Our Expertise


  • Collaborate with an extensive international network of pharmaceutical industry professionals and medical specialists
  • Identify areas of unmet medical need

  • Engage with regulatory authorities to agree scientific strategy

  • Direct on product development strategy including management, detailed analysis and reporting

  • Manage formulation development, clinical trial supplies, and transfer to commercial manufacturing

  • Design clinical studies and write protocols consistent with the current legislation

  • Audit CROs

  • Lead preclinical and clinical programmes in compliance with GXP

  • Secure agreement for Paediatric Investigation Plans (PIPs) and approval for clinical trials 

  • Obtain marketing authorisations

  • Consult on new chemical entities and existing formulations


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Other Specialites