Clinical Trial Manufacture

MedPharm has a GMP accredited and MHRA (MIAIMP) licensed manufacturing facility for the manufacture of topical and transdermal clinical supplies. Having a fully integrated service, that can now move from formulation design and assay validation all the way through to manufacture of clinical trial materials, is both convenient and cost effective for the client.

MedPharm is able to scale up all semi-solid dosage forms to a 50 Kg batch size and produce aerosols, solutions and other dosage forms on request. ICH stability and analytical testing, QP release and project management services are all available to aid the manufacturing process.

MedPharm can develop and validate quality assurance assays and in-process control for the client’s product and validate these in scale-up prior to performing a technical transfer to the finished products manufacturing facility.