A lot of people know that the US Department of Commerce publishes short research reports on the medical device industry in specific countries, but it's worth repeating in case you have not visited in some time. You can read regulatory process overviews on 20+ countries at the Learning Library on our website.
Software manufacturers whose products fall under Health Canada’s medical device classification system have until February or September 2011 to comply with new requirements set forth by the regulator.
Medical devices and IVD products able to pass muster with the US FDA and Health Canada may now enjoy de facto access to Mexico as well thanks to recent regulatory reforms. The Mexican Health Author
The UK’s Academy of Medical Sciences has issued a new report recommending the consolidation of medical research regulations and governance under a single entity. The Academy’s report, “A new Pathway for the Regulation and Governance of Health Research,” includes five key components: