Collaborate with HMC for valuable advice and input. By letting us accompany you from the very beginning of product development, your steps will be solid and cost-effective. We help you synchronize workflow, regulation and quality. By making sure your products always comply with the required regulations.

Learn more about product development.

By having a well-thought out strategy, you will minimize risks and quickly pass important milestones

Learn more about Regulatory strategy.

Help your clinical trials quickly succeed, eliminating unnecessary errors. Helps you develop studies in a timely and effective manner. We also create medical examination and survey sites and produce records with accurate and transparent data

Learn more about Clinical investigation.

We stay up-to-date with the latest regulations to help get your product submitted in a timely, correct manner. Limited returns and loss of time.

Learn more about regulatory submissions.

We rely on your system to create the most suitable management mechanism. Based on our proprietary approach, we implement Compliant, Lean, Integrated, and Custom QMSs. We will maintain all elements to ensure this quality system.

Learn more about Developing and ensuring the quality system.

We will carry out after-market monitoring activities and issue the necessary warnings. Make sure your business is sustainable.

Bring your medical equipment closer to your customers by talking to an HMC expert. HMC always has a team of experts available 24/7 to listen to its partners.

Learn more about Post-market surveillance.