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Analytical Services

By Penn Pharma

Working to ICH and cGMP guidelines, we provide analytical support for a wide variety of product development programmes. With an extensive range of fully qualified analytical equipment available as well as comprehensive stability studies expertise, we work closely with our clients to assist at every stage of the product development cycle.

With a track record of successful MHRA and FDA audits we offer clients complete piece of mind by providing analytical support for a wide variety of product development programmes.

Our clients ranges from small companies with specific development needs to multi-nationals requiring turnkey stability programs for commercial batches.

Penn also provides testing of product upon importation into the EU along with routine annual stability testing of commercialised products. Our analytical development experts not only support the Formulation Development process with protocol design, analysis and stability testing but also provide expert interpretation of data for clients. Our recently upgraded and expanded stability storage facilities provide more capacity and conditions to suit your specific requirements. This enables our Analytical Services team to provide a service second to none.

We:

  • Supply analytical method transfer protocols
  • Develop and validate analytical methodologies
  • Work according to ICH and cGMP guidelines
  • Offer a wide variety of techniques including HPLC, GC and LCMS
  • Offer cytotoxic and teratogenic compound testing
  • Provide strategies for testing of packaging configurations
  • Provide full ICH stability testing parameters
  • Provide expert documentation for regulatory submissions worldwide
  • Provide accurate analytical data to support development programmes