Pharmaceutical Quality Standards | GMP Requirements

Tergus Pharma and MedPharm are now one company!

The two premier topical experts have joined forces to create the world’s leading topical CDMO with global reach, experienced leadership, strong financial backing, and expanded end-to-end capabilities from early stage development through full commercial production of topical drug products.

Click here for the official press release.

We have an outstanding record of compliance with regulatory authorities, with a thorough understanding of the regulatory landscape and close relationships with the relevant bodies.

You can be confident that the manufacture and testing of your products at MedPharm facilities will meet all regulatory compliance requirements when required.

All activities at MedPharm are conducted in accordance with a single global harmonised Quality Management System (QMS) based on international Pharmaceutical Quality Standards. We have current certificates for working under cGMP and are licensed by the MHRA to manufacture clinical trial supplies worldwide.

All R&D studies are conducted following MedPharm’s quality management system that is compliant with ICH Q10. All Clinical (GMP) activities are performed in accordance with the requirements of cGMP.

Quality and Compliance