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Medpharm UK – Guildford

Formulation Development Facility

Unit 2, Surrey Research Park
Guildford, Surrey GU2 7AB, United Kingdom
Tel: +44 (0)1483 457 580

Overview

MedPharm’s Guildford facility is a 21,000 sq. ft. center of excellence for formulation development, located within the Surrey Research Park in the United Kingdom. Purpose-built to support the innovation, design, and evaluation of semi-solid and liquid pharmaceutical products, this facility plays a critical role in translating new drug concepts into clinical and commercial successes.

With deep experience in small molecules, biologics, and complex drug delivery systems, the Guildford site provides full-service CDMO support, from early formulation through to clinical trial material (CTM) manufacturing and stability testing.

Medpharm UK – Guildford

Specialized Laboratories

Formulation Development Labs – Prototype design, screening, and optimization
Process Development Labs – Scalable and GMP-aligned process evaluation
Characterization Suites – Rheology, viscosity, and texture profiling
Analytical Labs – Method development, validation, and release testing
Quality Control Labs – Batch release, raw material analysis, and stability testing

Key Capabilities

Formulation Development & Optimization

  • Semi-solid and liquid formulation expertise
  • Biologic and small molecule compatibility strategies
  • Prototype creation and proof-of-concept testing

Stability & Clinical Trial Manufacturing

  • ICH-compliant stability studies
  • Clinical batch production for Phase I–III
  • CTM packaging for global trial distribution

Analytical & Process Development

  • Analytical method development and validation
  • Process development with global tech transfer readiness
  • Support for scale-up and regulatory submissions

Quality & Compliance

The Guildford site operates under rigorous quality systems, with full adherence to MHRA and EU GMP standards. In-house QA and QC teams ensure each development milestone meets global expectations for safety, quality, and performance, supported by UK and EU QP oversight for clinical materials.


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