FDA 510k Submissions Guide: Free Kolabtree Whitepaper
510k submissions are an integral part of entering the USA medical device market, and help…
510k submissions are an integral part of entering the USA medical device market, and help…
Ensuring risk management in Medical device is a continuous process, and medical device manufacturers have a…
Kolabtree have recently published a whitepaper on ‘AI trends in medtech and digital healthcare’, authored…
Keeping up with timely EU MDR updates is crucial for medical device companies, enabling them…
In Part 1 of our series covering the major medtech, biotech and healthcare players in…
The Great Resignation might be the latest iteration, but the broader concept of a gig…
Looking to consult a medical content writer? Here’s an exhaustive guide on everything you need…
This article outlines the challenges medical device manufacturers are facing with EU MDR compliance and…
Mahasweta Pal, freelance medical writer on Kolabtree, provides a comprehensive comparison of medical device regulatory…
Mahasweta Pal, freelance medical writer on Kolabtree, writes about the essential skills medical device companies…
The medical devices industry is experiencing a massive transformation. Multi-billion dollar acquisitions in 2018 have…