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.

Over 30 Years
of Experience

Independent
Testing & Advice

Quality Assured
Solutions

Cost Effective
Services

Our Core Services

Lot and Batch Release Testing

Raw Material Testing

ICH Method Development and Validation

ICH Stability Testing and Storage

We are committed to providing laboratory services that deliver on the promise of quality, with focus on the provision of pharmaceutical testing in support of drug development with an emphasis on inhalation, oral dosage, parenteral and biologics.

Our highly skilled workforce provides a customer focused performance, working alongside you towards a common goal.

  • We offer a quality assured, confidential and cost-effective service. Our knowledgeable and helpful staff have over 30 years of experience providing independent testing and advice that is tailored to your specific needs.
  • You’ll have a direct line of contact to the project manager and analyst working on your project, always ensuring easy communication.
  • Our delivery system utilises the latest technology to deliver your analysis, with fast provision of results.
  • We provide regulatory compliant analytics in support of small and large molecule APIs, IMPs and finished products.

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.

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 and medical devices.

ICH Method Development and Validation

Method development and validation for a variety of platforms including HPLC, GC, UPLC, Dissolution and Elisa, supporting product development for a variety of pharmaceuticals, APIs and formulation types.

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.

Our cGMP pharmaceutical testing facility, located in Livingston, Scotland, is where we work together with our customers and partners. Building mutual trust through a sharing of knowledge, expertise and teamwork.