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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Environmental, Social and Governance (ESG) Medical Device Impact tips to ensure that your products fulfill compliance obligations. Major buyers request ESG reporting from suppliers as new and revised regulations require supply chain attention.
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Overview of 2024 Regulatory trends include QMSR, LDTs, FDA guidances, and timelines in the EU for MDR and IVDR.
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FDA Real-World Evidence Draft Guidance analysis identifies five key points to help understand the potential impact of the draft guidance.
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2024 resolutions our employees use to build a productive year ahead. May they help inspire you to start the New Year with positive goals.
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How a ready-made modular proof of concept system for rapid prototyping Point of Care Diagnostics can expedite and de-risk product development.
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The modular platform for transferring immunoassays acts as an intermediate bridge and is a significant step towards streamlining the product development process for diagnostics.
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Design and development insights for 3 areas of technology powering the future of cell and gene therapies (CGT) manufacturing: decentralized manufacturing, closed & automated systems and single-use technologies
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Medical device software is very diverse. In all this variety, one technology is ubiquitous: Git! Three eye-openers which help developers use Git better.
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Discover eleven essential medical device entrepreneur and founder traits used to successfully navigate the medical device industry.
