Good Laboratory Practice is good news for EPP and their clients

Published: 28 July 2021

The Medicines and Healthcare products Regulatory Agency (MHRA) has inspected and certified EPP Ltd as being GLP compliant - a position the company has held continuously since 2009.

The latest inspection covers diverse test areas such as Analytical Chemistry, Environmental Fate (eFate), Environmental Toxicity and Physical/Chemical Testing.

The MHRA is internationally recognised as being a global regulatory policy leader, acting as the UK Good Laboratory Practice Monitoring Authority (GLPMA) and therefore our clients can be assured that EPP conducts GLP studies to the highest standards in the world.

Good laboratory practice or GLP is a set of principles intended to assure the quality and integrity of non-clinical laboratory studies that are intended to support research or marketing permits for products regulated by government agencies.

Find out more about EPP GLP & Compliance

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EPP Ltd is a globally operating GLP Contract Research Organisation committed to providing superior quality across all aspects of their work. Continued Professional Development, training and mentoring underpin this quality and the company support their scientific and business teams to learn and improve.

The company celebrated 29 years of operation on 27 July 2021. The experienced staff work across three core areas - Analytical and Screening including REACH and 5-Batch; Environmental Sciences (eFate); and Process Research and Development (R&D).

EPP Ltd specialise in:

  • Custom synthesis of impurity, metabolite, and degradant reference standards
  • Re-certification of reference materials
  • GLP certification (with GLP NMR – qualitative analysis and on-site NMR)
  • Reference Standard Management Service
  • Synthesise stable labelled reference materials

For further information, please contact

Sharon McCluskie
Administration Manager

t: +44 (0)131 285 0566




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Managing Director: Rosie Newlands

T: +44 (0)131 285 0566

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