Supporting Drug Development, Improving Patient Outcomes
We are successful because of our People. We are Progressive in our way of thinking. We believe in our Principles.
We focus on the provision of pharmaceutical testing in support of drug development with an emphasis on inhalation, oral dosage, parenteral and biologics. We are committed to providing laboratory services that deliver on the promise of quality, through a highly skilled workforce and a customer focused performance working alongside you towards a common goal. Our cGMP pharmaceutical testing facility is located in Livingston, Scotland where we work together with our customers and partners building mutual trust through a sharing of knowledge, expertise and teamwork.
With over 30 years’ CRO experience of pharmaceutical testing, we provide regulatory compliant analytics in support of small and large molecule APIs, IMPs and finished products. We are committed to continuous improvement and development of our processes to create value propositions on behalf of our clients. Under inspection and approval of the MHRA and FDA, our pharmaceutical testing services include:
Lot and Batch Release Testing
Confirming every batch of medicine has the correct composition through documented and validated laboratory tests, before QP certification and release.
ICH Method Development and Validation
Method development and validation for a variety of platforms including HPLC, GC, UPLC, Dissolution and Elisa, support product development of a variety of pharmaceuticals, APIs and formulation types.
Raw Material Testing
Comprehensive testing as per pharmacopoeia (USP, EP, BP and JP) and to your specifications for analytical chemistry and microbiology for raw materials, APIs, finished products, packaging materials and medical devices.
ICH Stability Testing and Storage
Gathering data to determine an overall stability profile as described in ICH Q1A(R2) on Drug substance, drug product, combination devices, and raw materials.