HMC

The Advantage of Expertise

The 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.

Client First
The Hopkins MedTech Compliance always prioritizes their clients’ needs and believes that their clients’ success is the firm’s success.
A Holistic Approach
The Hopkins MedTech Compliance always takes a holistic approach to engagements with a strong emphasis on their FDA expertise. Beyond solving the immediate short-term challenges, we consider other hidden or future issues.
Partnership
The Hopkins MedTech Compliance’s in-house team fully integrates with the client’s stakeholders ensuring a close partnership and seamless management of the client’s most complex challenges.