phax pharma


Phax Pharma offers due diligence, audit, and pharmaceutical contractor management services.

Operating in an increasingly regulated industry we can bring a fresh and pragmatic approach to the necessary review of documents and facilities.

Our licensing experience with regulatory agencies means we are ideally positioned to provide advice or undertake due diligence on pharmaceutical products and active ingredients.

We offer a range of GMP and GDP services to make sure the necessary quality and regulatory requirements are being met.

And with the team’s industry knowledge in contracting out services, we have successfully identified and worked with a range of contract service providers across Europe.

Due Diligence

  • Potential licensing opportunities
  • Regulatory documents
  • CMC data evaluation
  • Drug master files

Quality Audits

  • Manufacturing sites
  • Analytical laboratories
  • Clinical trial supplies providers
  • Warehouses


  • Evaluation of contractors
  • Selection of contractors
  • Management of contractors


Documentation: CTD modules, orphan drug designation, clinical trial applications, more...

Scientific advice: Preparation, documents, presentation, communication, more...

Active ingredients: Drug master files, certificates of suitability, more...


Of interest

Quality ingredients & services


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