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.
-
Using a design approach to investigate the user’s needs provides a head start on ISO 60601 Ed. 3 and IEC 62366 medical devices
-
FDA 510(k) medical device submission tips and advice: being adequately prepared is essential for a smooth submission.
-
Inexpensive to build equipment with strategies and tips for successful medical device EMC compliance prescreening.
-
ISO 21500 and PMI provide guidance for Medical Device Development and Project Management Officer at StarFish Medical.
-
ISO 10993-1 and Biocompatibility impact on Medical Device Plans. Financial impact of additional Medical Device testing will have a cost.
-
Quality managers don’t have a magic wand to turn a bad product into a good one. Quality management needs an objective definition for quality.
-
Medical Device innovation and new product features must be balanced with an equally intense focus on Risk Analysis and Verification Testing.
-
A Project Management Office (PMO) supports Project Managers and promotes effective medical device development.
-
Seven tips for a smooth and successful outcome.to IEC 60601 Edition 3 submissions and electrical safety testing
