Device Advice by RQM+

Strategy for First-in-Human Studies (2/2) โ€“ MedTech CRO: Strategy Development Series


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*This video is part of our educational video series on clinical trials. Clips will cover three key areas: clinical trial strategy, clinical trial execution, and regulatory expertise in clinical trials. Please โ reach out to RQM+โ  if you need support with clinical trials.*


โ“ What are the CGMP principles and traceability requirements for ๐—ณ๐—ถ๐—ฟ๐˜€๐˜-๐—ถ๐—ป-๐—ต๐˜‚๐—บ๐—ฎ๐—ป ๐˜€๐˜๐˜‚๐—ฑ๐—ถ๐—ฒ๐˜€? How do you manage device iterations and site selection effectively?


๐ŸŽฌ The second video in our ๐— ๐—ฒ๐—ฑ๐—ง๐—ฒ๐—ฐ๐—ต ๐—–๐—ฅ๐—ข: ๐—ฆ๐˜๐—ฟ๐—ฎ๐˜๐—ฒ๐—ด๐˜† ๐——๐—ฒ๐˜ƒ๐—ฒ๐—น๐—ผ๐—ฝ๐—บ๐—ฒ๐—ป๐˜ ๐—ฆ๐—ฒ๐—ฟ๐—ถ๐—ฒ๐˜€ โ€“ ๐—ฆ๐˜๐—ฟ๐—ฎ๐˜๐—ฒ๐—ด๐˜† ๐—ณ๐—ผ๐—ฟ ๐—™๐—ถ๐—ฟ๐˜€๐˜-๐—ถ๐—ป-๐—›๐˜‚๐—บ๐—ฎ๐—ป ๐—ฆ๐˜๐˜‚๐—ฑ๐—ถ๐—ฒ๐˜€ (๐Ÿฎ/๐Ÿฎ) answers these questions. Once again, Jaishankar Kutty, Ph.D. is back with VP of Strategic Regulatory Affairs Sew-Wah Tay.


๐—ช๐—ฎ๐˜๐—ฐ๐—ต ๐˜๐—ผ ๐—น๐—ฒ๐—ฎ๐—ฟ๐—ป:

๐Ÿ“Œ The importance of CGMP principles and full traceability for FIH devices

๐Ÿ“Œ Managing device iterations in a 10-15 patient FIH study

๐Ÿ“Œ Key considerations for site and physician selection across different geographies


We hope these strategies help you navigate the complexities of FIH studies and ensure success. RQM+ is here to help if you need it.


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