Resource Centre
Discover a wealth of knowledge and insights from the experts at StarFish Medical. Our Resource Centre offers product development tips, reviews of new and cutting-edge technologies, and in-depth articles on regulatory updates and compliance in medical device development.
-
Summary of UK Medical Device Brexit Implications including high-level key points of the MHRA post-Brexit implementation plan.
-
FDA DHT Clinical Investigations examines the latest FDA draft guidance on Digital Health Technology for remote data acquisition in clinical investigations.
-
Analysis of QMSR ISO 13485:2016 Alignment in FDA proposed changes to Quality Management System Regulation for alignment with ISO 13485:2016.
-
Medical device cyber security: 2022 Update includes review of regulations and implications in an ever-evolving landscape of vulnerabilities.
-
StarFish employees share their bucket list vacation activities, including outdoor activities, family, travel, community, education.
-
Six principles to ensure your medical device project plan is useful and successful from a seasoned project manager.
-
Proven approach to medical device development risk management using an every day concept using plan, risks, opportunities, and actions.
-
Six common medical device product development destinations and overview of a High Level Program Planning (HLPP) approach.
-
Learn about the FDA’s 2023 guidance on premarket submissions for device software functions and its impact on the medical device industry.
