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Medical Device Management Services In North America
8 services found
by:TRIMEDX based inIndianapolis, INDIANA (USA)
REDUCE MEDICAL DEVICE SUPPLY CHAIN DISRUPTIONS AND CONTROL COSTS WITH TRIMEDX'S DEDICATED SUPPORT TEAM. Medical device supply chain management is one of the greatest disruptions to clinical engineering services. Non-standardized processes force biomed technicians to source parts for maintaining and ...
Manufactured by:Integrated Diagnostics Group, A division of Sanzay Corporation based inMiami Gardens, FLORIDA (USA)
IDG helps you approach the medical device market with ease of mind. We assist you with Medical Device and IVD Registration, local in-country representation, distributor qualification and quality system ...
Manufactured by:Nordson Medical based inHuntington Beach, CALIFORNIA (USA)
Nordson MEDICAL provides elegant and robust design and development solutions of finished medical ...
by:Emergo by UL based inAustin, TEXAS (USA)
Regulators in most medical device markets require registrants to meet post-market surveillance (PMS) obligations to maintain compliance. However, PMS rules can vary between different medical device markets, requiring manufacturers to develop tailored rather than one-size-fits-all approaches. With deep expertise in post-market surveillance requirements, Emergo is equipped to act as your compliance ...
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: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:Tietronix Software, Inc. based inHouston, TEXAS (USA)
Tietronix is a leading provider of cutting-edge software products and solutions for mission critical applications. Recognized for its expertise in process automation, medical device software development, and control systems for industries such as aerospace, defense, medical, and renewable energy. Tietronix gains its strength from a combination of experienced engineers, proven engineering ...
by:Emergo by UL based inAustin, TEXAS (USA)
It is easy to make mistakes in the regulatory process that can delay market entry or incur unnecessary costs. With help from Emergo’s medical device RA/QA consultants, you can pursue the most efficient regulatory route to approval and registration for your device, and maintain compliance with post-market requirements ...