on 6 March 2017 | By Jake O'Donnell
Medical device manufacturers need to carefully manage several important outward streams of information regarding their products. The regulatory community is generally most familiar with the data stream that relates to obtaining clearance to market devices, which involves...
Read Moreon 15 February 2016 | By Stephen Biernacki
About R&Q's Case Studies: We hope you find value in our second case study. View all of our available Case Studies. Subscribing to our blog is the best way to know when future case studies are available. Challenge Regulation doesn't have to be a barrier to innovation. A client...
Read Moreon 19 July 2013 | By Ryan Kasun
The latest mobile medical application news on the industry's collective mind is the issuance of an "It has come to our attention..." letter sent to Biosense Technologies in India, essentially questioning why Biosense has not obtained 510(k) clearance for their uChek mobile...
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