Analytical Services

We provide a wide range of services supporting each stage of the pre-clinical development process. Programmes have included:

  • Developing and validating methods for APIs, excipients, new drug products, and other materials
  • Supporting specialist manufacturing sites as part of their analytical resource
  • Stability and Leaching studies, multi condition store facilities are available on site
  • Routine release testing of APIs and products
We have wide experience developing methods for the Pharmaceutical, Medical Device and Healthcare industry sectors.
We are familiar with working with teams carrying out method validation work to meet regulatory requirements, and for internal cGMP needs.
Method verification is used to demonstrate that a standardised published method (e.g. Pharmacopoeial method) can be run effectively in a given laboratory.
We are able to support a full range of standard ICH conditions with both on site and off site qualified storage facilities.
We support release testing for clinical studies and more routine release.
As a company with a wide range of experience, particularly in the development field, we are used to working in multi-disciplinary teams across the UK and well beyond.
Problem solvers when your team need an answer