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November 23, 2021
On December 1st, join us as MIDI Medical Device Development Corp. and RQMIS Inc. present in a live #webinar "The Innovation Roadmap™ for Medical Device Development: Fostering Innovation & Optimum Programmatic Direction Under Strategic #Regulatory Deployment". Presented by Christopher Montalbano, CEO, MIDI Medical Device Development Corp., and Barry Sands, President, RQMIS.
September 1, 2021
If you want to verify if an establishment or product is registered and listed in the FDA, follow the advice of our experts!
August 24, 2021
The new In Vitro Diagnostic Medical Devices Regulation (2017/746/EU) (IVDR) bring EU legislation into line with technical advances changes in medical science, and progress in law making. At follow, you will have listed the changes that the IVDR involves for Invitro Diagnostic Manufacturers, and what IVDR manufactures should do to comply with it. RQMIS can help you providing In Vitro Diagnostic Medical Devices Regulation consultancy service to guide you in the new IVDR!
August 17, 2021
US FDA Establishment Registration & Medical Device Listing must be done between October 1 and December 31, 2021!
August 9, 2021
FDA De Novo 510K clearance RQMIS consultancy services - Success story by providing regulatory and quality remote full service support. RQMIS expert consultants worked to achieve the medical device manufacturer goals