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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Nick and Joris break down what a DHF is, why it's required, and how it plays a vital role throughout the development lifecycle.
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Common mistakes in medical device projects can create roadblocks that, if left unchecked, can snowball into costly setbacks.
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Overview of tools for Root Cause Analysis is an important tool in medical device development and manufacturing.
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elearning and LMS improve an employee’s ability to learn and adhere to the company QMS for medical device design and development.
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Nick and Joris dive into the surprising connection between rock bands and medical device safety. What do jelly beans and 1980s rock legends Van Halen have to do with developing safe and effective medical technologies? More than you might think.
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5 FDA Inspection tips from our QA/RA experts help make FDA inspections efficient, effective and successful.
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How QA/RA provides value to medical device project development projects and helps support Product Development and Manufacturing teams.
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Analysis of QMSR ISO 13485:2016 Alignment in FDA proposed changes to Quality Management System Regulation for alignment with ISO 13485:2016.
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Onsite or Virtual Audits uses an internal survey of QA/RA professionals to understand and weigh the pros and cons of virtual vs onsite audits.
