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.
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Design control shouldn’t inhibit creativity; it should enable it by providing a safety net in the form of a system to fall back on.
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Top 10 StarFish Medical blogs of 2017 feature a mix of regulatory, engineering, and practical information and advice for all levels of expertise.
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Enjoy our 2017 Readers' Choice Blogs and StarFish Medical articles, images, events and videos from our monthly newsletter.
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StarFish Medical videos help viewers learn medical device design, development and manufacture insights and tips from the people at StarFish.
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RoHS and REACH are two regulations that requires compliance if a company intends to sell in the European Union.
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Establishing supply chain controls to ensure reliable suppliers is critical to satisfy regulatory requirements for your device.
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Two ISO 13485:2016 section 7 changes impact your Quality Management System (QMS) are taking a risk based approach and documenting everything.
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How to handle recent medical product development regulatory changes under the 21st Century Cures Act and device exemption list.
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Start early to avoid surprises when preparing for MDR 2017/745. The new EU medical device regulations will come into full force in Q2 2020.
