- published: 28 Sep 2014
- views: 1517
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Title 21 CFR Part 11 is the part of Title 21 of the Code of Federal Regulations that establishes the United States Food and Drug Administration (FDA) regulations on electronic records and electronic signatures (ERES). Part 11, as it is commonly called, defines the criteria under which electronic records and electronic signatures are considered to be trustworthy, reliable and equivalent to paper records (Title 21 CFR Part 11 Section 11.1 (a)).
This video is targeted to blind users.
Attribution:
Article text available under CC-BY-SA
Creative Commons image source in video
In this video presentation, I've summarized 21 CFR part 11 guidelines into a easy presentation, followed by checklist for easy implementation. If you're interested to download this presentation, you could do so from website....
http://www.iricro.com/#!data-management/c73p
- published: 10 Nov 2013
- views: 7720
Learn about FDA 21 CFR Part 11 in layman's terms. --
If you’re involved with the life sciences industry, odds are you’ve heard the term “21 CFR Part 11.” You may have gathered that it’s a set of regulations related to computer systems, but unless you work in a compliance group, you might not understand what it’s about or why it’s important.
In our webinar, Sally Miranker, head of computer system validation in Perficient’s life sciences practice, “decoded” the secrets of 21 CFR Part 11.
Building on our popular blog post series, Sally explained the regulations in layman’s terms and offered implementation insights and case study examples.
To view this webinar in its entirety, please visit: http://www.perficient.com/Thought-Leadership/On-Demand-Webinars/2015/Decoding-21-CFR-Part-11
Stay on top of Life Sciences technologies by following us here:
Blog: http://blogs.perficient.com/lifesciences
Twitter: http://www.twitter.com/Perficient_LS
Facebook: http://www.facebook.com/Perficient
LinkedIn: http://www.linkedin.com/company/165444
Google+: https://plus.google.com/+Perficient
SlideShare: http://www.slideshare.net/PerficientInc
- published: 28 Apr 2015
- views: 881
Learn how pharmaceutical and medical device manufacturers can comply with the FDAs 21 CFR Part 11 regulations.
NiceLabel will explain what is needed to comply with regulations pertaining to electronic records, electronic signatures, and audit trails.
NiceLabel's Control Center Enterprise is the perfect software for FDA regulated companies that need label lifecycle management. Global organizations can consolidate their printing from each region and centralize on a single NiceLabel platform.
- published: 23 Jan 2014
- views: 5349
In this video, FDA compliance and Part 11 expert David Nettleton discusses the most common reasons why companies fail in ensuring their computer systems are validated, the time period for record retention, how to ensure software bought from vendors is Part 11 compliant and the need for training in this particular area.
Get more details - http://www.complianceonline.com/computer-system-validation-reduce-costs-and-avoid-483s-seminar-training-80005SEM-prdsm?channel=YT
- published: 21 Apr 2014
- views: 3731
FDA is increasing emphasis on scrutiny of computer systems validation and adherence of 21 CFR part 11 compliance validation to companies under FDA regulatory jurisdiction. A third of FDA’s recent warning letters have been with respect to improper or ineffective QA validation practices. Increasing use of automated manufacturing and quality system is forcing exposure of computer systems. Validated computerized systems are integral for producing accurate, reliable and consistent data. For many small to mid-sized organizations, meeting the regulatory requirements is a daunting task and 21 CFR Part 11 compliance is a major focus for audits.
This seminar will discuss the basics of 21 CFR Part 11 requirements and practical techniques for evaluation of the current compliance status of a given organization. You will hear about QA validation plans, user requirements, test plans, test reports, change controls, standard operating procedures, data backup and business continuity. Case studies will be used to highlight common issues and potential solutions. We will ensure your readiness for 21 CFR Part 11 compliance to confidently face the next FDA compliance audit.
- published: 28 Jan 2015
- views: 1276
21 CFR Part 11 is FDA regulation for electronic signatures and electronic records. It started by the Pharma - it is a good regulation for medical and Pharma companies but it is also a good guideline for other industries.
More Info - https://www.globalcompliancepanel.com
- published: 09 Feb 2015
- views: 568
More details: http://www.appfusions.com/display/PRT11J/Home
Eval at info@appfusions.com
• Compliance for Title 21 CFR Part 11
• Audit reports - printable view of all E-Signatures
• New "E-Signatures" tab in the "Activity" section for each issue
• User reauthenticates at each key stage to sign the transition
• Only successful authentication allows transition to next stage
- published: 28 Mar 2012
- views: 2563
This 21 CFR Part 11 training will analyze the regulations and provides concrete guidance on compliance for Electronic Medical Records.
For Information: http://www.complianceonline.com/21-cfr-part-11-compliance-for-electronic-medical-records-webinar-training-701217-prdw?channel=YT_701217
- published: 27 Jan 2016
- views: 62
View this webinar to learn all about the FCS Express Security System, with hundreds of permissions, extensive reporting, electronic signatures, and more. FCS Express provides all the functionality for your security and 21 CFR Part 11 requirements.
- published: 11 May 2015
- views: 86
Name: Validating SharePoint 2013 for 21 CFR Part 11 Environments
Date & Time: Friday, 9th August -11:00am EDT (New York), 4:00pm GMT (London), 5:00pm CET (Barcelona)
Presenter: Paul Fenton, President & CEO, Montrium
Summary:
When used as a system for managing regulated content and processes, SharePoint is subject to the requirements of 21 CFR Part 11 and related requirements. During this session we will review the approaches being taken by companies to validate their SharePoint environments, and emerge with a set of guidelines for a risk-based validation strategy for SharePoint. We will explore the differences in approach for cloud based environments versus on premise deployments. You will gain a clear understanding of why, when and how to validate SharePoint, and there will be a strong focus on reducing the time, cost and resources required to validate a SharePoint environment whilst providing maximum quality, control and ROI.
Topics will include:
- Managing and validating a mixed SharePoint environment that includes both controlled and non-controlled SharePoint sites
- Risk evaluation methods for SharePoint systems
- A Step by Step overview of the risk-based validation process following the GAMP5 model
- Implementing effective configuration and change control procedures for SharePoint-based systems
- SharePoint Online versus SharePoint on-premise
Find more at www.montrium.com
- published: 15 Aug 2013
- views: 6301
http://www.qsi-inc.com - Watch Our Video! Quality Systems Integrators has industry-leading 21 cfr part 11 software. We provide training and document
management solutions that save time and money.
- published: 01 Oct 2008
- views: 559
Title 21 CFR Part 11 of the Code of Federal Regulations deals with the Food and Drug Administration (FDA) guidelines on electronic records and electronic signatures in the United States. Part 11, as it is commonly called, defines the criteria under which electronic records and electronic signatures are considered to be trustworthy, reliable and equivalent to paper records (Title 21 CFR Part 11 Section 11.1 (a)).
Practically speaking, Part 11 requires drug makers, medical device manufacturers, biotech companies, biologics developers, CROs, and other FDA-regulated industries, with some specific exceptions, to implement controls, including audits, system validations, audit trails, electronic signatures, and documentation for software and systems involved in processing electronic data that are (a) required to be maintained by the FDA predicate rules or (b) used to demonstrate compliance to a predicate rule. A predicate rule is any requirement set forth in the Federal Food, Drug and Cosmetic Act, the Public Health Service Act, or any FDA regulation other than Part 11. [1]
This page contains text from Wikipedia, the Free Encyclopedia -
http://en.wikipedia.org/wiki/Title_21_CFR_Part_11
This article is licensed under the Creative Commons Attribution-ShareAlike 3.0 Unported License, which means that you can copy and modify it as long as the entire work (including additions) remains under this license.
This article is licensed under the Creative Commons Attribution-ShareAlike 3.0 Unported License, which means that you can copy and modify it as long as the entire work (including additions) remains under this license.
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6:52Title 21 CFR Part 11
Title 21 CFR Part 11Title 21 CFR Part 11
Title 21 CFR Part 11 is the part of Title 21 of the Code of Federal Regulations that establishes the United States Food and Drug Administration (FDA) regulations on electronic records and electronic signatures (ERES). Part 11, as it is commonly called, defines the criteria under which electronic records and electronic signatures are considered to be trustworthy, reliable and equivalent to paper records (Title 21 CFR Part 11 Section 11.1 (a)). This video is targeted to blind users. Attribution: Article text available under CC-BY-SA Creative Commons image source in video -
17:52Presentation on 21 CFR Part 11
Presentation on 21 CFR Part 11Presentation on 21 CFR Part 11
In this video presentation, I've summarized 21 CFR part 11 guidelines into a easy presentation, followed by checklist for easy implementation. If you're interested to download this presentation, you could do so from website.... http://www.iricro.com/#!data-management/c73p -
60:46Decoding 21 CFR Part 11
Decoding 21 CFR Part 11Decoding 21 CFR Part 11
Learn about FDA 21 CFR Part 11 in layman's terms. -- If you’re involved with the life sciences industry, odds are you’ve heard the term “21 CFR Part 11.” You may have gathered that it’s a set of regulations related to computer systems, but unless you work in a compliance group, you might not understand what it’s about or why it’s important. In our webinar, Sally Miranker, head of computer system validation in Perficient’s life sciences practice, “decoded” the secrets of 21 CFR Part 11. Building on our popular blog post series, Sally explained the regulations in layman’s terms and offered implementation insights and case study examples. To view this webinar in its entirety, please visit: http://www.perficient.com/Thought-Leadership/On-Demand-Webinars/2015/Decoding-21-CFR-Part-11 Stay on top of Life Sciences technologies by following us here: Blog: http://blogs.perficient.com/lifesciences Twitter: http://www.twitter.com/Perficient_LS Facebook: http://www.facebook.com/Perficient LinkedIn: http://www.linkedin.com/company/165444 Google+: https://plus.google.com/+Perficient SlideShare: http://www.slideshare.net/PerficientInc -
29:40FDA 21 CFR Part 11 Webinar
FDA 21 CFR Part 11 WebinarFDA 21 CFR Part 11 Webinar
Learn how pharmaceutical and medical device manufacturers can comply with the FDAs 21 CFR Part 11 regulations. NiceLabel will explain what is needed to comply with regulations pertaining to electronic records, electronic signatures, and audit trails. NiceLabel's Control Center Enterprise is the perfect software for FDA regulated companies that need label lifecycle management. Global organizations can consolidate their printing from each region and centralize on a single NiceLabel platform. -
5:57FDA Compliance Expert on Computer System Validation and 21 CFR Part 11
FDA Compliance Expert on Computer System Validation and 21 CFR Part 11FDA Compliance Expert on Computer System Validation and 21 CFR Part 11
In this video, FDA compliance and Part 11 expert David Nettleton discusses the most common reasons why companies fail in ensuring their computer systems are validated, the time period for record retention, how to ensure software bought from vendors is Part 11 compliant and the need for training in this particular area. Get more details - http://www.complianceonline.com/computer-system-validation-reduce-costs-and-avoid-483s-seminar-training-80005SEM-prdsm?channel=YT -
32:57Webinar on 21 CFR Part 11 - Road to Successful FDA Compliance
Webinar on 21 CFR Part 11 - Road to Successful FDA ComplianceWebinar on 21 CFR Part 11 - Road to Successful FDA Compliance
FDA is increasing emphasis on scrutiny of computer systems validation and adherence of 21 CFR part 11 compliance validation to companies under FDA regulatory jurisdiction. A third of FDA’s recent warning letters have been with respect to improper or ineffective QA validation practices. Increasing use of automated manufacturing and quality system is forcing exposure of computer systems. Validated computerized systems are integral for producing accurate, reliable and consistent data. For many small to mid-sized organizations, meeting the regulatory requirements is a daunting task and 21 CFR Part 11 compliance is a major focus for audits. This seminar will discuss the basics of 21 CFR Part 11 requirements and practical techniques for evaluation of the current compliance status of a given organization. You will hear about QA validation plans, user requirements, test plans, test reports, change controls, standard operating procedures, data backup and business continuity. Case studies will be used to highlight common issues and potential solutions. We will ensure your readiness for 21 CFR Part 11 compliance to confidently face the next FDA compliance audit. -
11:0121 CFR Part 11: Complete Manual For Compliance Success - GlobalCompliancePanel Virtual Seminar
21 CFR Part 11: Complete Manual For Compliance Success - GlobalCompliancePanel Virtual Seminar21 CFR Part 11: Complete Manual For Compliance Success - GlobalCompliancePanel Virtual Seminar
21 CFR Part 11 is FDA regulation for electronic signatures and electronic records. It started by the Pharma - it is a good regulation for medical and Pharma companies but it is also a good guideline for other industries. More Info - https://www.globalcompliancepanel.com -
0:55CFR Part 11 Compliance E-Signatures (FDA) for JIRA
CFR Part 11 Compliance E-Signatures (FDA) for JIRACFR Part 11 Compliance E-Signatures (FDA) for JIRA
More details: http://www.appfusions.com/display/PRT11J/Home Eval at info@appfusions.com • Compliance for Title 21 CFR Part 11 • Audit reports - printable view of all E-Signatures • New "E-Signatures" tab in the "Activity" section for each issue • User reauthenticates at each key stage to sign the transition • Only successful authentication allows transition to next stage -
2:40What's This 21 CFR Part 11 Thing
What's This 21 CFR Part 11 ThingWhat's This 21 CFR Part 11 Thing
This 21 CFR Part 11 training will analyze the regulations and provides concrete guidance on compliance for Electronic Medical Records. For Information: http://www.complianceonline.com/21-cfr-part-11-compliance-for-electronic-medical-records-webinar-training-701217-prdw?channel=YT_701217 -
30:29Security, Logging, and 21 CFR Part 11 compliance in FCS Express 5
Security, Logging, and 21 CFR Part 11 compliance in FCS Express 5Security, Logging, and 21 CFR Part 11 compliance in FCS Express 5
View this webinar to learn all about the FCS Express Security System, with hundreds of permissions, extensive reporting, electronic signatures, and more. FCS Express provides all the functionality for your security and 21 CFR Part 11 requirements. -
57:42Validating SharePoint 2013 for 21 CFR Part 11 Environments Webinar
Validating SharePoint 2013 for 21 CFR Part 11 Environments WebinarValidating SharePoint 2013 for 21 CFR Part 11 Environments Webinar
Name: Validating SharePoint 2013 for 21 CFR Part 11 Environments Date & Time: Friday, 9th August -11:00am EDT (New York), 4:00pm GMT (London), 5:00pm CET (Barcelona) Presenter: Paul Fenton, President & CEO, Montrium Summary: When used as a system for managing regulated content and processes, SharePoint is subject to the requirements of 21 CFR Part 11 and related requirements. During this session we will review the approaches being taken by companies to validate their SharePoint environments, and emerge with a set of guidelines for a risk-based validation strategy for SharePoint. We will explore the differences in approach for cloud based environments versus on premise deployments. You will gain a clear understanding of why, when and how to validate SharePoint, and there will be a strong focus on reducing the time, cost and resources required to validate a SharePoint environment whilst providing maximum quality, control and ROI. Topics will include: - Managing and validating a mixed SharePoint environment that includes both controlled and non-controlled SharePoint sites - Risk evaluation methods for SharePoint systems - A Step by Step overview of the risk-based validation process following the GAMP5 model - Implementing effective configuration and change control procedures for SharePoint-based systems - SharePoint Online versus SharePoint on-premise Find more at www.montrium.com -
1:2721 cfr part 11 software
21 cfr part 11 software21 cfr part 11 software
http://www.qsi-inc.com - Watch Our Video! Quality Systems Integrators has industry-leading 21 cfr part 11 software. We provide training and document management solutions that save time and money.
-
Title 21 CFR Part 11
Title 21 CFR Part 11 is the part of Title 21 of the Code of Federal Regulations that establishes the United States Food and Drug Administration (FDA) regulations on electronic records and electronic signatures (ERES). Part 11, as it is commonly called, defines the criteria under which electronic records and electronic signatures are considered to be trustworthy, reliable and equivalent to paper records (Title 21 CFR Part 11 Section 11.1 (a)). This video is targeted to blind users. Attribution: Article text available under CC-BY-SA Creative Commons image source in video -
Presentation on 21 CFR Part 11
In this video presentation, I've summarized 21 CFR part 11 guidelines into a easy presentation, followed by checklist for easy implementation. If you're interested to download this presentation, you could do so from website.... http://www.iricro.com/#!data-management/c73p -
Decoding 21 CFR Part 11
Learn about FDA 21 CFR Part 11 in layman's terms. -- If you’re involved with the life sciences industry, odds are you’ve heard the term “21 CFR Part 11.” You may have gathered that it’s a set of regulations related to computer systems, but unless you work in a compliance group, you might not understand what it’s about or why it’s important. In our webinar, Sally Miranker, head of computer system validation in Perficient’s life sciences practice, “decoded” the secrets of 21 CFR Part 11. Building on our popular blog post series, Sally explained the regulations in layman’s terms and offered implementation insights and case study examples. To view this webinar in its entirety, please visit: http://www.perficient.com/Thought-Leadership/On-Demand-Webinars/2015/Decoding-21-CFR-Part-11 Stay... -
FDA 21 CFR Part 11 Webinar
Learn how pharmaceutical and medical device manufacturers can comply with the FDAs 21 CFR Part 11 regulations. NiceLabel will explain what is needed to comply with regulations pertaining to electronic records, electronic signatures, and audit trails. NiceLabel's Control Center Enterprise is the perfect software for FDA regulated companies that need label lifecycle management. Global organizations can consolidate their printing from each region and centralize on a single NiceLabel platform. -
FDA Compliance Expert on Computer System Validation and 21 CFR Part 11
In this video, FDA compliance and Part 11 expert David Nettleton discusses the most common reasons why companies fail in ensuring their computer systems are validated, the time period for record retention, how to ensure software bought from vendors is Part 11 compliant and the need for training in this particular area. Get more details - http://www.complianceonline.com/computer-system-validation-reduce-costs-and-avoid-483s-seminar-training-80005SEM-prdsm?channel=YT -
Webinar on 21 CFR Part 11 - Road to Successful FDA Compliance
FDA is increasing emphasis on scrutiny of computer systems validation and adherence of 21 CFR part 11 compliance validation to companies under FDA regulatory jurisdiction. A third of FDA’s recent warning letters have been with respect to improper or ineffective QA validation practices. Increasing use of automated manufacturing and quality system is forcing exposure of computer systems. Validated computerized systems are integral for producing accurate, reliable and consistent data. For many small to mid-sized organizations, meeting the regulatory requirements is a daunting task and 21 CFR Part 11 compliance is a major focus for audits. This seminar will discuss the basics of 21 CFR Part 11 requirements and practical techniques for evaluation of the current compliance status of a given org... -
21 CFR Part 11: Complete Manual For Compliance Success - GlobalCompliancePanel Virtual Seminar
21 CFR Part 11 is FDA regulation for electronic signatures and electronic records. It started by the Pharma - it is a good regulation for medical and Pharma companies but it is also a good guideline for other industries. More Info - https://www.globalcompliancepanel.com -
CFR Part 11 Compliance E-Signatures (FDA) for JIRA
More details: http://www.appfusions.com/display/PRT11J/Home Eval at info@appfusions.com • Compliance for Title 21 CFR Part 11 • Audit reports - printable view of all E-Signatures • New "E-Signatures" tab in the "Activity" section for each issue • User reauthenticates at each key stage to sign the transition • Only successful authentication allows transition to next stage -
What's This 21 CFR Part 11 Thing
This 21 CFR Part 11 training will analyze the regulations and provides concrete guidance on compliance for Electronic Medical Records. For Information: http://www.complianceonline.com/21-cfr-part-11-compliance-for-electronic-medical-records-webinar-training-701217-prdw?channel=YT_701217 -
Security, Logging, and 21 CFR Part 11 compliance in FCS Express 5
View this webinar to learn all about the FCS Express Security System, with hundreds of permissions, extensive reporting, electronic signatures, and more. FCS Express provides all the functionality for your security and 21 CFR Part 11 requirements. -
Validating SharePoint 2013 for 21 CFR Part 11 Environments Webinar
Name: Validating SharePoint 2013 for 21 CFR Part 11 Environments Date & Time: Friday, 9th August -11:00am EDT (New York), 4:00pm GMT (London), 5:00pm CET (Barcelona) Presenter: Paul Fenton, President & CEO, Montrium Summary: When used as a system for managing regulated content and processes, SharePoint is subject to the requirements of 21 CFR Part 11 and related requirements. During this session we will review the approaches being taken by companies to validate their SharePoint environments, and emerge with a set of guidelines for a risk-based validation strategy for SharePoint. We will explore the differences in approach for cloud based environments versus on premise deployments. You will gain a clear understanding of why, when and how to validate SharePoint, and there will be a stro... -
21 cfr part 11 software
http://www.qsi-inc.com - Watch Our Video! Quality Systems Integrators has industry-leading 21 cfr part 11 software. We provide training and document management solutions that save time and money.
Title 21 CFR Part 11
- Order: Reorder
- Duration: 6:52
- Updated: 28 Sep 2014
- views: 1517
Title 21 CFR Part 11 is the part of Title 21 of the Code of Federal Regulations that establishes the United States Food and Drug Administration (FDA) regulation...
Title 21 CFR Part 11 is the part of Title 21 of the Code of Federal Regulations that establishes the United States Food and Drug Administration (FDA) regulations on electronic records and electronic signatures (ERES). Part 11, as it is commonly called, defines the criteria under which electronic records and electronic signatures are considered to be trustworthy, reliable and equivalent to paper records (Title 21 CFR Part 11 Section 11.1 (a)).
This video is targeted to blind users.
Attribution:
Article text available under CC-BY-SA
Creative Commons image source in video
wn.com/Title 21 Cfr Part 11
Title 21 CFR Part 11 is the part of Title 21 of the Code of Federal Regulations that establishes the United States Food and Drug Administration (FDA) regulations on electronic records and electronic signatures (ERES). Part 11, as it is commonly called, defines the criteria under which electronic records and electronic signatures are considered to be trustworthy, reliable and equivalent to paper records (Title 21 CFR Part 11 Section 11.1 (a)).
This video is targeted to blind users.
Attribution:
Article text available under CC-BY-SA
Creative Commons image source in video
- published: 28 Sep 2014
- views: 1517
Presentation on 21 CFR Part 11
- Order: Reorder
- Duration: 17:52
- Updated: 10 Nov 2013
- views: 7720
In this video presentation, I've summarized 21 CFR part 11 guidelines into a easy presentation, followed by checklist for easy implementation. If you're interes...
In this video presentation, I've summarized 21 CFR part 11 guidelines into a easy presentation, followed by checklist for easy implementation. If you're interested to download this presentation, you could do so from website....
http://www.iricro.com/#!data-management/c73p
wn.com/Presentation On 21 Cfr Part 11
In this video presentation, I've summarized 21 CFR part 11 guidelines into a easy presentation, followed by checklist for easy implementation. If you're interested to download this presentation, you could do so from website....
http://www.iricro.com/#!data-management/c73p
- published: 10 Nov 2013
- views: 7720
Decoding 21 CFR Part 11
- Order: Reorder
- Duration: 60:46
- Updated: 28 Apr 2015
- views: 881
Learn about FDA 21 CFR Part 11 in layman's terms. --
If you’re involved with the life sciences industry, odds are you’ve heard the term “21 CFR Part 11.” You m...
Learn about FDA 21 CFR Part 11 in layman's terms. --
If you’re involved with the life sciences industry, odds are you’ve heard the term “21 CFR Part 11.” You may have gathered that it’s a set of regulations related to computer systems, but unless you work in a compliance group, you might not understand what it’s about or why it’s important.
In our webinar, Sally Miranker, head of computer system validation in Perficient’s life sciences practice, “decoded” the secrets of 21 CFR Part 11.
Building on our popular blog post series, Sally explained the regulations in layman’s terms and offered implementation insights and case study examples.
To view this webinar in its entirety, please visit: http://www.perficient.com/Thought-Leadership/On-Demand-Webinars/2015/Decoding-21-CFR-Part-11
Stay on top of Life Sciences technologies by following us here:
Blog: http://blogs.perficient.com/lifesciences
Twitter: http://www.twitter.com/Perficient_LS
Facebook: http://www.facebook.com/Perficient
LinkedIn: http://www.linkedin.com/company/165444
Google+: https://plus.google.com/+Perficient
SlideShare: http://www.slideshare.net/PerficientInc
wn.com/Decoding 21 Cfr Part 11
Learn about FDA 21 CFR Part 11 in layman's terms. --
If you’re involved with the life sciences industry, odds are you’ve heard the term “21 CFR Part 11.” You may have gathered that it’s a set of regulations related to computer systems, but unless you work in a compliance group, you might not understand what it’s about or why it’s important.
In our webinar, Sally Miranker, head of computer system validation in Perficient’s life sciences practice, “decoded” the secrets of 21 CFR Part 11.
Building on our popular blog post series, Sally explained the regulations in layman’s terms and offered implementation insights and case study examples.
To view this webinar in its entirety, please visit: http://www.perficient.com/Thought-Leadership/On-Demand-Webinars/2015/Decoding-21-CFR-Part-11
Stay on top of Life Sciences technologies by following us here:
Blog: http://blogs.perficient.com/lifesciences
Twitter: http://www.twitter.com/Perficient_LS
Facebook: http://www.facebook.com/Perficient
LinkedIn: http://www.linkedin.com/company/165444
Google+: https://plus.google.com/+Perficient
SlideShare: http://www.slideshare.net/PerficientInc
- published: 28 Apr 2015
- views: 881
FDA 21 CFR Part 11 Webinar
- Order: Reorder
- Duration: 29:40
- Updated: 23 Jan 2014
- views: 5349
Learn how pharmaceutical and medical device manufacturers can comply with the FDAs 21 CFR Part 11 regulations.
NiceLabel will explain what is needed to comply...
Learn how pharmaceutical and medical device manufacturers can comply with the FDAs 21 CFR Part 11 regulations.
NiceLabel will explain what is needed to comply with regulations pertaining to electronic records, electronic signatures, and audit trails.
NiceLabel's Control Center Enterprise is the perfect software for FDA regulated companies that need label lifecycle management. Global organizations can consolidate their printing from each region and centralize on a single NiceLabel platform.
wn.com/Fda 21 Cfr Part 11 Webinar
Learn how pharmaceutical and medical device manufacturers can comply with the FDAs 21 CFR Part 11 regulations.
NiceLabel will explain what is needed to comply with regulations pertaining to electronic records, electronic signatures, and audit trails.
NiceLabel's Control Center Enterprise is the perfect software for FDA regulated companies that need label lifecycle management. Global organizations can consolidate their printing from each region and centralize on a single NiceLabel platform.
- published: 23 Jan 2014
- views: 5349
FDA Compliance Expert on Computer System Validation and 21 CFR Part 11
- Order: Reorder
- Duration: 5:57
- Updated: 21 Apr 2014
- views: 3731
In this video, FDA compliance and Part 11 expert David Nettleton discusses the most common reasons why companies fail in ensuring their computer systems are val...
In this video, FDA compliance and Part 11 expert David Nettleton discusses the most common reasons why companies fail in ensuring their computer systems are validated, the time period for record retention, how to ensure software bought from vendors is Part 11 compliant and the need for training in this particular area.
Get more details - http://www.complianceonline.com/computer-system-validation-reduce-costs-and-avoid-483s-seminar-training-80005SEM-prdsm?channel=YT
wn.com/Fda Compliance Expert On Computer System Validation And 21 Cfr Part 11
In this video, FDA compliance and Part 11 expert David Nettleton discusses the most common reasons why companies fail in ensuring their computer systems are validated, the time period for record retention, how to ensure software bought from vendors is Part 11 compliant and the need for training in this particular area.
Get more details - http://www.complianceonline.com/computer-system-validation-reduce-costs-and-avoid-483s-seminar-training-80005SEM-prdsm?channel=YT
- published: 21 Apr 2014
- views: 3731
Webinar on 21 CFR Part 11 - Road to Successful FDA Compliance
- Order: Reorder
- Duration: 32:57
- Updated: 28 Jan 2015
- views: 1276
FDA is increasing emphasis on scrutiny of computer systems validation and adherence of 21 CFR part 11 compliance validation to companies under FDA regulatory ju...
FDA is increasing emphasis on scrutiny of computer systems validation and adherence of 21 CFR part 11 compliance validation to companies under FDA regulatory jurisdiction. A third of FDA’s recent warning letters have been with respect to improper or ineffective QA validation practices. Increasing use of automated manufacturing and quality system is forcing exposure of computer systems. Validated computerized systems are integral for producing accurate, reliable and consistent data. For many small to mid-sized organizations, meeting the regulatory requirements is a daunting task and 21 CFR Part 11 compliance is a major focus for audits.
This seminar will discuss the basics of 21 CFR Part 11 requirements and practical techniques for evaluation of the current compliance status of a given organization. You will hear about QA validation plans, user requirements, test plans, test reports, change controls, standard operating procedures, data backup and business continuity. Case studies will be used to highlight common issues and potential solutions. We will ensure your readiness for 21 CFR Part 11 compliance to confidently face the next FDA compliance audit.
wn.com/Webinar On 21 Cfr Part 11 Road To Successful Fda Compliance
FDA is increasing emphasis on scrutiny of computer systems validation and adherence of 21 CFR part 11 compliance validation to companies under FDA regulatory jurisdiction. A third of FDA’s recent warning letters have been with respect to improper or ineffective QA validation practices. Increasing use of automated manufacturing and quality system is forcing exposure of computer systems. Validated computerized systems are integral for producing accurate, reliable and consistent data. For many small to mid-sized organizations, meeting the regulatory requirements is a daunting task and 21 CFR Part 11 compliance is a major focus for audits.
This seminar will discuss the basics of 21 CFR Part 11 requirements and practical techniques for evaluation of the current compliance status of a given organization. You will hear about QA validation plans, user requirements, test plans, test reports, change controls, standard operating procedures, data backup and business continuity. Case studies will be used to highlight common issues and potential solutions. We will ensure your readiness for 21 CFR Part 11 compliance to confidently face the next FDA compliance audit.
- published: 28 Jan 2015
- views: 1276
21 CFR Part 11: Complete Manual For Compliance Success - GlobalCompliancePanel Virtual Seminar
- Order: Reorder
- Duration: 11:01
- Updated: 09 Feb 2015
- views: 568
21 CFR Part 11 is FDA regulation for electronic signatures and electronic records. It started by the Pharma - it is a good regulation for medical and Pharma com...
21 CFR Part 11 is FDA regulation for electronic signatures and electronic records. It started by the Pharma - it is a good regulation for medical and Pharma companies but it is also a good guideline for other industries.
More Info - https://www.globalcompliancepanel.com
wn.com/21 Cfr Part 11 Complete Manual For Compliance Success Globalcompliancepanel Virtual Seminar
21 CFR Part 11 is FDA regulation for electronic signatures and electronic records. It started by the Pharma - it is a good regulation for medical and Pharma companies but it is also a good guideline for other industries.
More Info - https://www.globalcompliancepanel.com
- published: 09 Feb 2015
- views: 568
CFR Part 11 Compliance E-Signatures (FDA) for JIRA
- Order: Reorder
- Duration: 0:55
- Updated: 28 Mar 2012
- views: 2563
More details: http://www.appfusions.com/display/PRT11J/Home
Eval at info@appfusions.com
• Compliance for Title 21 CFR Part 11
• Audit reports - printable view ...
More details: http://www.appfusions.com/display/PRT11J/Home
Eval at info@appfusions.com
• Compliance for Title 21 CFR Part 11
• Audit reports - printable view of all E-Signatures
• New "E-Signatures" tab in the "Activity" section for each issue
• User reauthenticates at each key stage to sign the transition
• Only successful authentication allows transition to next stage
wn.com/Cfr Part 11 Compliance E Signatures (Fda) For Jira
More details: http://www.appfusions.com/display/PRT11J/Home
Eval at info@appfusions.com
• Compliance for Title 21 CFR Part 11
• Audit reports - printable view of all E-Signatures
• New "E-Signatures" tab in the "Activity" section for each issue
• User reauthenticates at each key stage to sign the transition
• Only successful authentication allows transition to next stage
- published: 28 Mar 2012
- views: 2563
What's This 21 CFR Part 11 Thing
- Order: Reorder
- Duration: 2:40
- Updated: 27 Jan 2016
- views: 62
This 21 CFR Part 11 training will analyze the regulations and provides concrete guidance on compliance for Electronic Medical Records.
For Information: http://...
This 21 CFR Part 11 training will analyze the regulations and provides concrete guidance on compliance for Electronic Medical Records.
For Information: http://www.complianceonline.com/21-cfr-part-11-compliance-for-electronic-medical-records-webinar-training-701217-prdw?channel=YT_701217
wn.com/What's This 21 Cfr Part 11 Thing
This 21 CFR Part 11 training will analyze the regulations and provides concrete guidance on compliance for Electronic Medical Records.
For Information: http://www.complianceonline.com/21-cfr-part-11-compliance-for-electronic-medical-records-webinar-training-701217-prdw?channel=YT_701217
- published: 27 Jan 2016
- views: 62
Security, Logging, and 21 CFR Part 11 compliance in FCS Express 5
- Order: Reorder
- Duration: 30:29
- Updated: 11 May 2015
- views: 86
View this webinar to learn all about the FCS Express Security System, with hundreds of permissions, extensive reporting, electronic signatures, and more. FCS Ex...
View this webinar to learn all about the FCS Express Security System, with hundreds of permissions, extensive reporting, electronic signatures, and more. FCS Express provides all the functionality for your security and 21 CFR Part 11 requirements.
wn.com/Security, Logging, And 21 Cfr Part 11 Compliance In Fcs Express 5
View this webinar to learn all about the FCS Express Security System, with hundreds of permissions, extensive reporting, electronic signatures, and more. FCS Express provides all the functionality for your security and 21 CFR Part 11 requirements.
- published: 11 May 2015
- views: 86
Validating SharePoint 2013 for 21 CFR Part 11 Environments Webinar
- Order: Reorder
- Duration: 57:42
- Updated: 15 Aug 2013
- views: 6301
Name: Validating SharePoint 2013 for 21 CFR Part 11 Environments
Date & Time: Friday, 9th August -11:00am EDT (New York), 4:00pm GMT (London), 5:00pm CET (Barc...
Name: Validating SharePoint 2013 for 21 CFR Part 11 Environments
Date & Time: Friday, 9th August -11:00am EDT (New York), 4:00pm GMT (London), 5:00pm CET (Barcelona)
Presenter: Paul Fenton, President & CEO, Montrium
Summary:
When used as a system for managing regulated content and processes, SharePoint is subject to the requirements of 21 CFR Part 11 and related requirements. During this session we will review the approaches being taken by companies to validate their SharePoint environments, and emerge with a set of guidelines for a risk-based validation strategy for SharePoint. We will explore the differences in approach for cloud based environments versus on premise deployments. You will gain a clear understanding of why, when and how to validate SharePoint, and there will be a strong focus on reducing the time, cost and resources required to validate a SharePoint environment whilst providing maximum quality, control and ROI.
Topics will include:
- Managing and validating a mixed SharePoint environment that includes both controlled and non-controlled SharePoint sites
- Risk evaluation methods for SharePoint systems
- A Step by Step overview of the risk-based validation process following the GAMP5 model
- Implementing effective configuration and change control procedures for SharePoint-based systems
- SharePoint Online versus SharePoint on-premise
Find more at www.montrium.com
wn.com/Validating Sharepoint 2013 For 21 Cfr Part 11 Environments Webinar
Name: Validating SharePoint 2013 for 21 CFR Part 11 Environments
Date & Time: Friday, 9th August -11:00am EDT (New York), 4:00pm GMT (London), 5:00pm CET (Barcelona)
Presenter: Paul Fenton, President & CEO, Montrium
Summary:
When used as a system for managing regulated content and processes, SharePoint is subject to the requirements of 21 CFR Part 11 and related requirements. During this session we will review the approaches being taken by companies to validate their SharePoint environments, and emerge with a set of guidelines for a risk-based validation strategy for SharePoint. We will explore the differences in approach for cloud based environments versus on premise deployments. You will gain a clear understanding of why, when and how to validate SharePoint, and there will be a strong focus on reducing the time, cost and resources required to validate a SharePoint environment whilst providing maximum quality, control and ROI.
Topics will include:
- Managing and validating a mixed SharePoint environment that includes both controlled and non-controlled SharePoint sites
- Risk evaluation methods for SharePoint systems
- A Step by Step overview of the risk-based validation process following the GAMP5 model
- Implementing effective configuration and change control procedures for SharePoint-based systems
- SharePoint Online versus SharePoint on-premise
Find more at www.montrium.com
- published: 15 Aug 2013
- views: 6301
21 cfr part 11 software
- Order: Reorder
- Duration: 1:27
- Updated: 01 Oct 2008
- views: 559
http://www.qsi-inc.com - Watch Our Video! Quality Systems Integrators has industry-leading 21 cfr part 11 software. We provide training and document
manageme...
http://www.qsi-inc.com - Watch Our Video! Quality Systems Integrators has industry-leading 21 cfr part 11 software. We provide training and document
management solutions that save time and money.
wn.com/21 Cfr Part 11 Software
http://www.qsi-inc.com - Watch Our Video! Quality Systems Integrators has industry-leading 21 cfr part 11 software. We provide training and document
management solutions that save time and money.
- published: 01 Oct 2008
- views: 559
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6:52
Title 21 CFR Part 11
Title 21 CFR Part 11 is the part of Title 21 of the Code of Federal Regulations that estab...
published: 28 Sep 2014
Title 21 CFR Part 11
Title 21 CFR Part 11
- Report rights infringement
- published: 28 Sep 2014
- views: 1517
17:52
Presentation on 21 CFR Part 11
In this video presentation, I've summarized 21 CFR part 11 guidelines into a easy presenta...
published: 10 Nov 2013
Presentation on 21 CFR Part 11
Presentation on 21 CFR Part 11
- Report rights infringement
- published: 10 Nov 2013
- views: 7720
60:46
Decoding 21 CFR Part 11
Learn about FDA 21 CFR Part 11 in layman's terms. --
If you’re involved with the life sci...
published: 28 Apr 2015
Decoding 21 CFR Part 11
Decoding 21 CFR Part 11
- Report rights infringement
- published: 28 Apr 2015
- views: 881
29:40
FDA 21 CFR Part 11 Webinar
Learn how pharmaceutical and medical device manufacturers can comply with the FDAs 21 CFR ...
published: 23 Jan 2014
FDA 21 CFR Part 11 Webinar
FDA 21 CFR Part 11 Webinar
- Report rights infringement
- published: 23 Jan 2014
- views: 5349
5:57
FDA Compliance Expert on Computer System Validation and 21 CFR Part 11
In this video, FDA compliance and Part 11 expert David Nettleton discusses the most common...
published: 21 Apr 2014
FDA Compliance Expert on Computer System Validation and 21 CFR Part 11
FDA Compliance Expert on Computer System Validation and 21 CFR Part 11
- Report rights infringement
- published: 21 Apr 2014
- views: 3731
32:57
Webinar on 21 CFR Part 11 - Road to Successful FDA Compliance
FDA is increasing emphasis on scrutiny of computer systems validation and adherence of 21 ...
published: 28 Jan 2015
Webinar on 21 CFR Part 11 - Road to Successful FDA Compliance
Webinar on 21 CFR Part 11 - Road to Successful FDA Compliance
- Report rights infringement
- published: 28 Jan 2015
- views: 1276
11:01
21 CFR Part 11: Complete Manual For Compliance Success - GlobalCompliancePanel Virtual Seminar
21 CFR Part 11 is FDA regulation for electronic signatures and electronic records. It star...
published: 09 Feb 2015
21 CFR Part 11: Complete Manual For Compliance Success - GlobalCompliancePanel Virtual Seminar
21 CFR Part 11: Complete Manual For Compliance Success - GlobalCompliancePanel Virtual Seminar
- Report rights infringement
- published: 09 Feb 2015
- views: 568
0:55
CFR Part 11 Compliance E-Signatures (FDA) for JIRA
More details: http://www.appfusions.com/display/PRT11J/Home
Eval at info@appfusions.com
•...
published: 28 Mar 2012
CFR Part 11 Compliance E-Signatures (FDA) for JIRA
CFR Part 11 Compliance E-Signatures (FDA) for JIRA
- Report rights infringement
- published: 28 Mar 2012
- views: 2563
2:40
What's This 21 CFR Part 11 Thing
This 21 CFR Part 11 training will analyze the regulations and provides concrete guidance o...
published: 27 Jan 2016
What's This 21 CFR Part 11 Thing
What's This 21 CFR Part 11 Thing
- Report rights infringement
- published: 27 Jan 2016
- views: 62
30:29
Security, Logging, and 21 CFR Part 11 compliance in FCS Express 5
View this webinar to learn all about the FCS Express Security System, with hundreds of per...
published: 11 May 2015
Security, Logging, and 21 CFR Part 11 compliance in FCS Express 5
Security, Logging, and 21 CFR Part 11 compliance in FCS Express 5
- Report rights infringement
- published: 11 May 2015
- views: 86
57:42
Validating SharePoint 2013 for 21 CFR Part 11 Environments Webinar
Name: Validating SharePoint 2013 for 21 CFR Part 11 Environments
Date & Time: Friday, 9th...
published: 15 Aug 2013
Validating SharePoint 2013 for 21 CFR Part 11 Environments Webinar
Validating SharePoint 2013 for 21 CFR Part 11 Environments Webinar
- Report rights infringement
- published: 15 Aug 2013
- views: 6301
1:27
21 cfr part 11 software
http://www.qsi-inc.com - Watch Our Video! Quality Systems Integrators has industry-leading...
published: 01 Oct 2008
21 cfr part 11 software
21 cfr part 11 software
- Report rights infringement
- published: 01 Oct 2008
- views: 559
Title 21 CFR Part 11...
Presentation on 21 CFR Part 11...
Decoding 21 CFR Part 11...
FDA 21 CFR Part 11 Webinar...
FDA Compliance Expert on Computer System Validatio...
Webinar on 21 CFR Part 11 - Road to Successful FDA...
21 CFR Part 11: Complete Manual For Compliance Suc...
CFR Part 11 Compliance E-Signatures (FDA) for JIRA...
What's This 21 CFR Part 11 Thing...
Security, Logging, and 21 CFR Part 11 compliance i...
Validating SharePoint 2013 for 21 CFR Part 11 Envi...
21 cfr part 11 software...
photo: Creative Commons / Gage Skidmore
[VIDEOS]: Behind-The-Scenes Scenario May Prevent Trump, Clinton Presidency: Report
Edit WorldNews.com 18 May 2016
Current Democratic frontrunner Hillary Clinton also wins on the Democratic side.Republican strategist Liz Mair told Mother Jones the option being discussed would see popular third-party candidates – say Mitt Romney running in Utah or Sen ... Should that happen, the president would be chosen by the Republican-led U.S. House of Representatives. Is such a plan legal? The 12th Amendment to the U.S. Constitution allows for the process ... ....
photo: AP / Elaine Thompson
“In New Republican Party We Trust” As Democrats Face Contested Convention
Edit WorldNews.com 18 May 2016
Article by WN.com Correspondent Dallas DarlingIt was Benjamin Franklin who wrote the sardonic proverb ... To be sure, Sen ... This is why he can challenge the 9/11, Iraq, NATO, European allies and Free Trade narratives, why he can repeatedly change his answers, and why he gets a free pass with his views towards Russia, Planned Parenthood and a national healthcare system. Even William F ... They also blame her for the deaths of four U.S....
photo: NASA / JPL-Caltech/ SETI Institute
A mysterious ocean on a frozen moon just became our best shot at finding alien life
Edit Business Insider 18 May 2016
"We’re studying an alien ocean using methods developed to understand the movement of energy and nutrients in Earth’s own systems," Steve Vance, a planetary scientist at JPL and lead author of the new study, said in a press release ... This process is also likely responsible for cracks in the moon's surface ... "Whether or not life and biological processes complete the circuit is part of what motivates our exploration of Europa," says Hand ... ....
photo: AP / Olamikan Gbemiga
'First Chibok girl found' in Nigeria
Edit BBC News 18 May 2016
One of the Chibok girls has been found, the first since their capture by Boko Haram militants in 2014, activists say ... ....
photo: WN / Imran Nissar
US scientists say major earthquake likely in Jammu & Kashmir
Edit The Times of India 18 May 2016
New geologic mapping in the Himalayan mountains of Kashmir suggests that the region is ripe for a major earthquake that could endanger the lives of as many as a million people, according to an Oregon State University statement ... The 2005 Kashmir earthquake killed about 80,000 people in Pakistan and India ... The fault hasn't slipped for a long time, which means the potential for a large earthquake is strong ... It's a matter of when." ... RELATED....
« back to news headlines
Local youths’ views on TV programs part of festival (Southern Illinois University System)
Edit Public Technologies 19 May 2016
-- Findings about children's television programs judged by local youths earlier this year will be part of an international festival where the focus is on promoting quality television for children throughout the world. The results will be part of the Prix Jeunesse International Festival --'What it means to be me ... category for 11-15 year olds....
Leechburg SD parents, board members want answers amid latest controversy
Edit WPXI 19 May 2016
Kline and a school board member who spoke with Channel 11 News Wednesday said there’s a pattern of the district not keeping taxpayers in the loop ... Despite multiple calls over the past two days, no one from the district agreed to an on-camera interview with Channel 11 News ... School board member Anthony Shea told Channel 11 News over the phone Wednesday that he's outraged by the latest allegations....
The Biggest M&A; Deals Of 2015
Edit Forbes 19 May 2016
Target.Allergan. Acquirer.Pfizer. Deal value, including debt.$160 billion. Date. 11/23/15. Merger. Deal value, stock-for-stock.$130 billion. Date.12/11/2015. Target.SABMiller. Acquirer.Anheuser-Busch InBev. Deal value, including debt.$107 billion. Date.11/11/2015. Target.BG Group PLC. Acquirer.Royal Dutch Shell PLC ... Date.4/8/2015. Target ... Acquirer....
The Latest: Larsen surprised by inclusion on Trump list
Edit The Associated Press 19 May 2016
One of the 11 judges named by Donald Trump on Wednesday as a potential replacement for the late Antonin Scalia says her inclusion on the list took her by surprise ... attorney in Missouri is among 11 potential Supreme Court justices presumptive Republican presidential nominee Donald Trump has released ... The Republican senator said in a statement Wednesday that the people he knows on Trump's list of 11 potential U.S....
Greenberg Traurig Received Multiple Honors at the 2016 Turnaround Atlas Awards (Greenberg Traurig LLP)
Edit Public Technologies 19 May 2016
(Source. Greenberg Traurig LLP) ... The firm was honored with the following awards ... Steinberg, Andrew R ... 'Chapter 11 Restructuring of the Year - Middle Markets' award for its role in Global Geophysical Services' Chapter 11 Plan of Reorganization ... 'Retail Services Turnaround of the Year' award for its role in Frederick's of Hollywood's Chapter 11 Plan of Reorganization and acquisition by Authentic Brands Group....
IFES Testifies on Capitol Hill on “Democracy Support Strategies in Africa” (IFES - International Foundation for Electoral Systems)
Edit Public Technologies 19 May 2016
In many parts of the world, IFES also works with its Consortium for Elections and Political Process Strengthening (CEPPS) partners - the International Republican Institute and the National Democratic Institute - under USAID's Elections and Political Transitions mechanism (EPT) on comprehensive democracy, human rights, and governance (DRG) programming....
National Get Outdoors Day at Fort Vancouver National Historic Site Highlights Outdoor Recreation in the Northwest (NPS - National Park Service)
Edit Public Technologies 19 May 2016
(Source. NPS - National Park Service) News Release Date.. May 18, 2016 ... National Get Outdoors Day (GO Day) will bring community partners together to celebrate healthy, active, outdoor fun at Fort Vancouver National Historic Site (NHS) from 10 am to 3 pm, Saturday, June 11, 2016 ... National Get Outdoors Day (GO Day) ... WHAT ... WHEN. 10 am to 3 pm, Saturday, June 11, 2016 ... Entrance to the reconstructed Fort Vancouver will also be free on June 11....
CorVel Announces Fiscal Earnings Release Webcast (CorVel Corporation)
Edit Public Technologies 19 May 2016
(Source. CorVel Corporation). IRVINE, CALIFORNIA, May 18, 2016 - In conjunction with CorVel Corporation's (NASDAQ. CRVL) fiscal year earnings release, CorVel will be conducting a conference call that will be broadcast live over the Internet on Thursday, June 2 at 11.30 am Eastern Time. Event.. CorVel Announces Fiscal Earnings Release Webcast. Host.. Gordon Clemons, Chief Executive Officer. Date. Thursday, June 2, 2016 ... 11.30 am Eastern Time....
A taste of local produce in a food desert Gray Street Farmers Market returns... (University of Louisville)
Edit Public Technologies 19 May 2016
(Source. University of Louisville). LOUISVILLE, Ky ... 'Farmers markets are great ways to bring fresh, healthy foods into our neighborhoods ... - 2.00 p.m., the market includes 11 vendorsfrom throughout Kentucky and Indiana ... The market also has established a new partnership with the Kentucky Cooperative Extension Service's Nutrition Education Program, and will co-sponsor meal-sampling events on June 9, July 14, and August 11 ... STAY CONNECTED ... ###....
Bank of England's chief economist calls for more simple pension system
Edit The Guardian 19 May 2016
He called for simplification as part of the process of eroding the “great divide” between the public and bankers and other financial professionals caused by the 2008 crash ... “Of course, part of the reason so many members of the public find finance difficult is because it is difficult – and, sometimes at least, it is made deliberately so. Related ... Twitter ... “The way maths is taught may be part of the problem here ... ....
Bank of England's top economist in call to make pensions simpler
Edit Belfast Telegraph 19 May 2016
He called for simplification as part of the process of eroding the "great divide" between the public and bankers and other financial professionals caused by the 2008 crash ... "Of course, part of the reason so many members of the public find finance difficult is because it is difficult - and, sometimes at least, it is made deliberately so," he said ... "The way maths is taught may be part of the problem here ... ....
Buy Local Summit Moved to Mutare
Edit Topix 19 May 2016
Other key presenters expected to speak at the event to be held from the June 8-11 are Industry and Commerce Minister Mike Bimha and Reserve Bank of Zimbabwe Governor Dr John Mangudya.Mines and Mining Development Minister Walter Chidhakwa and other key Government officials, private sector leaders and the academia are also expected to participate in the 2016 event's economic discussions ... ....
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