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Quality and regulatory services for medical devices

ProductLife Group provides full product lifecycle support from Design to Post Market, and for all domains of Medical Devices, Combined Devices, SAMDs.

Thorough understanding of Business processes for managing communication between the different stake-holders involved in a project – such as: clinical, regulatory, Quality, PMS team, manufacturing, and commercial. Advising clients on their processes or redefining and formalizing the processes with clients.

Thanks to cross functional expertise in regulatory, safety, and quality, information management, in both Medical devices and Pharma Environment, PLG develops pragmatic strategies consulting for new challenges facing companies placing medical devices, combined devices, Startups with innovative solutions.

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