- published: 14 Apr 2014
- views: 5289
If you are thinking of supplying a therapeutic good, then you are a potential sponsor. To help you get started, watch this video to find out: * the six steps you need to follow when considering making an application to the TGA * where to find relevant information about different types of goods * what legal and financial responsibilities you need to be aware of * where to get more information on the regulatory process. * Make sure you also read the Overview of Supplying Therapeutic Goods in Australia.
Here's another BRAND NEW clip from Ross' new DVD Nonsensory Overload! The DVD is out NOW - buy yours on Amazon (http://goo.gl/kZ6Bh) This clip again comes from the Canberra performance, with Ross finding out more about the world of therapeutic goods administration from an audience member. Don't forget to Like/Share/Subscribe! ---- The official YouTube channel of international man of comedy, Ross Noble. To find out more about Ross Noble visit his Wikipedia page: http://en.wikipedia.org/wiki/Ross_Noble Check out Ross Noble's official website: http://www.rossnoble.co.uk Ross Noble is also on Myspace: http://www.myspace.com/officiallynoble You can also show support by following Ross Noble on twitter @realrossnoble: http://twitter.com/realrossnoble Like Ross Noble on Facebook: http:/...
Watch a 40 second introduction about the work of Australia’s medicines and medical devices regulator - the Therapeutic Goods Administration, including what types of products we regulate. For more details watch the full videos about the role of the Therapeutic Goods Administration for consumers and also for health professionals: https://www.bit.ly/edu-consumers https://www.bit.ly/edu-healthprofessionals
All therapeutic goods have some level of risk. Our role is to ensure that, on balance, the benefits outweigh any known risks. Watch this video to find out: * how we weigh the potential benefits of a product against the risks the different processes associated with lower risk and higher risk goods * what we do if a problem is identified after a product has been released to the market * how you can help us to monitor safety by reporting problems with therapeutic goods.
An overview of how to search the TGA website - focusing on the ARTG and other specialised databases, and where to search for specific information. More videos are available to help you understand the work of the TGA.
Course Description: This course describes conformity assessment and examines the process for obtaining a Conformity Assessment Certificate from the Australian Therapeutic Goods Administration (TGA), including the timeframes for assessment. It also explains what happens once an application is deemed successful or not and the ongoing responsibilities of the manufacturer after a certificate has been obtained. Learn more at: http://www.wmdo.org/course-detail.aspx?id=153
http://MedicalDevicesGroup.net Sydney-based regulatory affairs expert Arthur Brandwood discusses the recent changes made by the Australian Therapeutic Goods Administration (TGA). He also covers: • Australia’s aggressive deregulatory agenda • The Australian tax incentive (43.5% for R&D; expenditure) • The simple process for regulation of clinical trials in Australia • TGA’s web based submission process for device approvals
If you are a manufacturer, sponsor or agent who wants to use our online services you will need to use our TGA Business Services site. Watch this video to find out about: - How each user will have a personalised view - The different roles allocated to users - including drafter, submitter, financial or administrator, or any combination of these roles - How news and details of your organisation are displayed - Viewing a history of the various interactions your organisation has had with TGA Business Services.
Making sure you have access to therapeutic goods that are safe and good quality-meaning that they have been properly formulated and manufactured to certain standards-is an important and complex job. Watch this video to find out: • who we are and where the regulatory system originated • how the regulatory system operates • what products we regulate, and the different processes applied to lower and higher risk products • how you can help us to improve public health and safety.
The NZ Government is trying to change the way in which all Natural Health Products (NHPs) are regulated. They plan to treat Natural Health Products as drugs and give the power to control them to the Foreign Australian Therapeutic Goods Administration (TGA). 46 min indepth presentation by Amy Adams. The DVD was produced by NZ Health Trust in association with New Health New Zealand, it may be copied, distributed and Broadcast in its entirety free of charge - anything less than full reproduction or transmission of the contents requires the approval of the NZ Health Trust NZ Health Trust Webmaster: Paul Fahey
Course Description: Course Description: This course examines the fees and charges related to making applications to either the Australian Therapeutic Goods Administration (TGA) for conformity assessment certificates or the Australian Register of Therapeutic Goods (ARTG) for the inclusion of IVDs. It also describes the provisions available for reduced fees and the circumstances in which they may be granted. Learn more at: http://www.wmdo.org/course-detail.aspx?id=154
Video taken of an eastern brown snake at the entrance of the Therapeutic Goods Administration (TGA) building in Symonston, Canberra, Australia
A leaked judgement shows the TGA upheld a new wave of complaints about the advertising of Swisse products. *Correction, the TGA is the Therapeutic Goods Administration NOT association.* http://www.theage.com.au/national/swisse-ads-did-mislead-as-complaint-is-upheld-again-20130607-2nvok.html
0:00:00Introduction Richard Saunders 0:05:40Maynard's Spooky Action... Australian Skeptics National Convention - Maynard chats with...Dr Krissy Wilson, Kieran Dennis and Jayson Cooke 0:22:45Reality Bites... with Joanne Benhamu - Joanne comments on the recent recall of apricot kernels due to risk of cyanide toxicity and the history of claims about them as a cancer cure. 0:29:05 The Think Tank - This time we invade the home of Eran Segev to chat about the Therapeutic Goods Administration (TGA), Post-Fukushima 'anti-radiation' pills condemned by scientists, Bisphenol A (BPA) scare and the winners and losers at the 2011 Australian Skeptics Convention. With Dr Rachie Dunlop, Joanne Benhamu and Richard Saunders.
Do we really need supplements? Is the supplement industry safe? High-Quality Manufacturing is a necessity due to the nature of a very poorly regulated supplement industry. USANA’s founder, Myron Wentz, Ph.D., created this science-based company because he had a vision of a world free from pain and suffering. A world free from disease. And he knew science and high-quality manufacturing could help him bring his vision to life. That’s why our commitment to quality goes beyond the formulas we create. We manufacture more than 90 percent of our products in our own manufacturing facilities so we can control the entire process, from raw ingredient to finished supplement. John Cuomo, Ph.D., USANA’s executive director of product development and technology, explains, “The main reason to manuf...
Ray Thorpe Founder of the Happy Herb Company talks Drug Law Reform On Tuesday 31st May, 2016 at 8 am Melbourne (Monday 11 pm BST), CCN's We Are The Ones We've Been Waiting For's hostess, Eilish De Avalon chatted with Ray Thorpe Founder of Happy Herb Company about Drug Law Reform and his foray into politics, as an Independent in the New South Wales Senate. Eilish De Avalon, CCN's Hostess of We Are The Ones We've Been Waiting For Ray Thorpe is not only an entrepreneur he's also an avid Plant Activist advocating for the de-criminalisation of Medical Cannabis and other Medicinal Herbs. Ray Thorpe's vision is a properly informed public using safe non-addictive plants for medicine and recreation. Compare this to the current reality, where alcohol, tobacco and dangerous chemicals are consumed on ...
Question and Answer session Dr Eric Green, Director of the US National Human Genetics Research Institute (NHGRI), visited NHMRC on 8 August 2012. NHGRI is one of the 27 institutes that comprise the US National Institutes of Health (NIH) and NHGRI led the NIH's contribution to the International Human Genome Project, which had as its primary goal the sequencing of the human genome. In addition to meeting with NHMRC CEO, Professor Warwick Anderson, and senior NHMRC staff to discuss the two agencies shared interests in genome research and its application to human health, Dr Green gave a presentation titled "Entering the Era of Genomic Medicine: Research Opportunities and Challenges". The presentation was attended by NHMRC staff and invited guests from the Australian National University, the ...
Presentation Dr Eric Green, Director of the US National Human Genetics Research Institute (NHGRI), visited NHMRC on 8 August 2012. NHGRI is one of the 27 institutes that comprise the US National Institutes of Health (NIH) and NHGRI led the NIH's contribution to the International Human Genome Project, which had as its primary goal the sequencing of the human genome. In addition to meeting with NHMRC CEO, Professor Warwick Anderson, and senior NHMRC staff to discuss the two agencies shared interests in genome research and its application to human health, Dr Green gave a presentation titled "Entering the Era of Genomic Medicine: Research Opportunities and Challenges". The presentation was attended by NHMRC staff and invited guests from the Australian National University, the Department of H...
Dear friends This is an extract from our web site about Arbonne purity policy. None like this on the market: It is an equal opportunity employer : http://www.youtube.com/watch?v=KATAgtEdGmI About Our Products At Arbonne, beauty begins with premium botanical ingredients, innovative scientific discovery, and an unwavering commitment to pure, safe and beneficial products. Arbonne creates personal care and wellness products that preserve and enhance the skin, body and mind for an integrative approach to beauty. Working closely with scientists around the world and our Arbonne Institute of Research and Development (AIRD®) facility in Switzerland, we continually explore and develop scientifically advanced, botanically based proprietary formulas that meet our exacting standards for quality, saf...
Australia continues to be an attractive medical device market. It is sophisticated, transparent and for implantable devices there are reimbursement schemes that deliver certainty of pricing. The national regulator continues to improve processes to streamline registration of medium to low risk produces based on European (CE) certification evidence, although there's some way to go on dealing with backlogs of technical file desk audits ("application Audits") for certain higher risk devices. TGA continues to update the regulatory framework, with a current consultation on a key guidance for clinical evidence requirements, a new notification scheme for custom made devices and participation in the MDSAP program - which provides opportunities for faster registrations in Australia. If you're look...
Australians spend over $1.2 billion a year on complementary medicines. Many people use them in conjunction with orthodox medicines but do not necessarily disclose this to their doctor. The widespread availability of complementary medicines through the internet, pharmacies, supermarkets and health-food stores means that consumer information regarding quality, safety and efficacy can be confusing and sometimes misleading. The use and acceptance of complementary medicines in the community is often in contrast to the scepticism and opposition of many primary health care practitioners. This program aims to provide health professionals with the best advice for effective and informed health care practice on complementary medicines. The program covers: • Types of complementary medicines in Aust...