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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RoHS and REACH compliance is required to sell equipment or consumer parts with hazardous materials in EU, China, Korea, United States and Canada.
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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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Top 3 root causes of design transfer problems are identified by the author with suggestions for corrective actions to mitigate the problems.
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Applying Process Failure Modes and Effects Analysis (PFMEA) efficiently to Medtech manufacturing process will greatly improve effectiveness.
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A world class medtech supply chain is made on a foundation of controls, knowledge and planning. Expert tips for optimization.
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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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Overview of magnetism and rare earth magnets with a novel medical application homogenizing tissue samples (IE liver or brain) using rare earth magnets.
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Define medical device ID strategy early, A strategy document can quickly align a large interdisciplinary team on a product’s design direction.
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Any medical device connected to a hospital network or the cloud may be exposed to some form of medical device cyber attack.
