HMC has a full range of resources, including collaborative labs and in-house engineers to accompany you from the very first steps of drug development. With the Functional Service Provider model, you can get advice, perform testing, access expert data, and much more.

Learn more about Drug 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.

With our solid experience, we will help you create a suitable plan to lead to success. HMC's team of scientists will help you categorize products, define system requirements, create budgets and action systems for management, answer any questions you need.

Learn more about Regulatory strategy.

This is the step to help you shape the way to commercialize the product. We will help you arrange a pre-IND meeting with the FDA and prepare all the documents you need.

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 relationships to help you monitor your site, check for GCP, and other critical components.

Learn more about Clinical investigation.

We have a proprietary methodology to establish a customized quality system tailored to you while meeting international standards. Not only does it help you pass pre-approval checks, but it also gives you an added competitive edge.

Learn more about Developing and ensuring the quality system.

We will maintain every aspect of your quality management system. Make sure your products are sustainable to standards and regulations.

HMC will continue to accompany you to develop your career. When you invest in a new project, we will continue to monitor the safety of your existing products.

Kickstart your success by talking to HMC. We always have a team of experts available 24/7 to listen to its partners.