What I am about to share with you is a guide to medical device regulatory classification. In this guide, I will provide you with a step-by-step approach for determining how your medical device will be ...
Developers with the mHealth Regulatory Coalition may have done some important heavy lifting in the struggle to clarify the U.S. Food and Drug Administration's regulation of mobile devices. The ...
Dublin, Nov. 05, 2025 (GLOBE NEWSWIRE) -- The "Mobile Medical Device Apps and the FDA - Classification, Regulatory Requirements and Cybersecurity" training has been added to ResearchAndMarkets.com's ...
The Gastroenterology and Urology Devices Panel of the US Food and Drug Administration's (FDA's) Medical Devices Advisory Committee deliberated yesterday on the classification of 4 categories of ...
As the biopharma space gets more competitive and the days of blockbuster drugs seem further in the rearview, biopharma companies are investing in digital to find new and innovative ways to ...
Key opportunities in the European medical devices market include leveraging comprehensive regulatory guides to streamline product registration across diverse countries, utilizing soft skills for ...
The medical device market has grown rapidly in the past decade and shows no sign of slowing down. An increasing number of companies have tapped the Asian region to manufacture medical devices. Many ...
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