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Emergo is the largest EU AR for medical devices and IVDs, representing more than 1,000 device companies worldwide. We offer a new premium EU AR service designed for manufacturers looking for more than just an EU AR.
Our resource centers for Europe, Asia and Latin America compile regulatory updates and insights, white papers, process charts, videos, and available medical device consulting services for fast access to region-specific market and regulatory information.
Emergo: medical device consultants for QA/RA, device registration, clinical trials, reimbursement and distribution consulting. Offices worldwide.
12 de oct. de 2021 · Read more about the benefits of hiring an independent firm to act as your EC REP in Europe. Why choose Emergo as your European Authorized Representative? Emergo is the largest Authorized Representative for medical devices and IVDs, representing more than 1,000 device companies worldwide.
Emergo by UL | 15,298 followers on LinkedIn. Emergo provides quality and regulatory compliance consulting to medical device and IVD companies.
Emergo provides quality and regulatory compliance consulting to medical device and IVD companies. We assist with medical device registration/approval, regulatory strategy, ISO 13485 and QMS...
European member states by means of a new regulatory body called the Medical Device Coordination Group (MDCG). The objective of the MDCG is to foster cooperation between the member states while increasing the Commission’s power to act as needed in acute cases. The MDCG is in the process of establishing sub-groups consisting of various ...
