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.