Corate 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. Make sure your products always comply with the required regulations.

Learn more about product development.

We can support you through the entire preclinical research process. Compliance is guaranteed from initial animal model identification to final clinical report generation.

Learn more about Preclinical Research.

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

Learn more about Regulatory strategy.

This is an important step for you to shape your path to market. We'll help you prepare this entire important step, including formulating FDA questions, documentation, and insights.

Learn more about Pre-IND.

HMC is your key partner in obtaining regulatory approval. We prepare a complete package of documents, shaping clinical trials to ensure success. In addition, we use our relationship to help you monitor your site, check for GCP, and other critical components.

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 take steps to monitor after the market and report vigilance. Make it easier for you to commercialize your product.

Save your cost and time by contacting us.

Learn more about Post-market surveillance.