MedPharm Limited is a member of the Medicines and Healthcare Products Regulatory Agency (MHRA) Good Laboratory Practice (GLP) programme ensuring that all work is performed in accordance with the principles of Good Laboratory Practice. In addition we are accredited for Good Manufacturing Practce (GMP) by the MHRA.

The MedPharm Quality System has been developing their quality assurance procedures over a number of years to meet the stringent Quality Assurance requirements demanded by our clients in the drug delivery and formulation business.

As a service provider in clinical and preclinical research activities, MedPharm offers flexibility in the management of your development process, according to the highest quality standards. Our pre-clinical services constitute a remarkable range of experience and expertise which includes qualified pharmacists, pharmaceutical scientists, microbiologists, biotechnologists, chemical and physiochemical analysts with experience in numerous therapeutic areas.

As part of our ongoing commitment to GLP and GMP we provide full training for staff and are continuously upgrading and evaluating their skills. Our independent QA department Tower Mains Limited with over 20 years of auditing and Quality Assurance experience routinely audits our facilities, systems and procedures. This ensures that MedPharm always operates within current compliance regulations. To date MedPharm has undergone numerous client audits and as part of our commitment to their continued success we are happy to accommodate their auditing requirements in any way possible.

This pro-active approach ensures an environment of scientific excellence and encourages all staff to be actively involved in the continual improvement of the Quality System within MedPharm.