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Medical Device Management Services In Europe
5 services found
by:NSAI Inc. based inNashua, NEW HAMPSHIRE (USA)
ISO 13485 is a necessary certification for medical device manufacturers. It proves that you have a quality manufacturing process and the management standards in place to maintain high quality. ISO 13485 certification is the first step towards achieving compliance with European, Canadian and other regulatory requirements for ...
Manufactured by:IMPLANET based inMartillac, FRANCE
Medical device flow management requires heavy means and procedures to ensure traceability, quality and product integrity, due to the sensitivity of their nature and ...
by:Evamed based inHerouville-Saint-Clair, FRANCE
Evamed has developed an online data collection tool specifically for medical devices. The project manager, with his data-management team, accompany you in: Creating an online template, Configuration of the eCRF during a session between Evamed and the sponsor, Customizing the eCRF for your study, Implementation of automatic ...
Manufactured by:MediPurpose based inDuluth, GEORGIA (US) (USA)
The MediPurpose™ Medical Device Innovation division collaborates with medical device inventors and innovators to take new medical devices from concept to commercialization—bringing together financing, proven medical device development methodology and global experience to help ensure success. Taking a new medical invention from concept to commercialization can be a difficult process, ...
by:Metecon GmbH based inMannheim, GERMANY
An audit is the most effective method to establish certainty that you as the manufacturer or distributor of medical devices are in the position to meet all requirements. Metecon offers comprehensive support in this regard with a wealth of experience and know-how. Take a moment to get an overview of our services. And if you see any need, we look forward to discussing a solution with ...