Hopkins MedTech Compliance

Hopkins MedTech Compliance is a CRO dedicated for IVD Clinical Performance Studies for FDA & EU and regulatory filing. OneStop Shop for Your Global Clinical Study. Hopkins MedTech Compliance helps medical device companies rapidly access the industry's best consultants, contractors, and candidates. Our resources assist in every stage of the product lifecycle, from clinical development to commercialization, with a focus in Quality Assurance, Regulatory Affairs, and Clinical Operations. HMC provides assistance in applying for EUA、premarket notice 510K by FDA、CE mark by European Commission and MDR. Finding top talent in the hyper-competitive life science industries gets harder each day. With over 1,500 resources worldwide, 85 of whom are former FDA, we meet your precise resourcing needs through a fast, convenient talent selection process supported by a Total Quality Guarantee.

• Employees 6
• Founded 2020