Australian TGA collaborates with UK agency
This article was originally published in RAJ Devices
Executive Summary
The Australian Therapeutic Goods Administration has signed a memorandum of understanding with the UK Medicines and Healthcare Products Regulatory Agency to establish a framework for co-operation in the regulation of therapeutic products, including medical devices, human blood products and medicinal products1.
You may also be interested in...
Stakeholders Deliberate on Developing US Social Media Guidance
Jeanette Marchant reports on discussions at the US Food and Drug Administration public hearing on how drug and medical device companies should use the internet and social media to promote regulated products.
Stakeholders Deliberate on Developing US Social Media Guidance
Jeanette Marchant reports on discussions at the US Food and Drug Administration public hearing on how drug and medical device companies should use the internet and social media to promote regulated products.
Asian group identifies criteria for device nomenclature system
The Asian Harmonization Working Party agreed six criteria for a medical device nomenclature system at its 14th meeting in Hong Kong on 4-7 November 20091. The requirements ? which will help in the selection of a nomenclature system service provider ? cover charges for using the system; its governance; ownership of the database; response times to requests; the system’s future development; and further use.