Summary of Services Offered

Philip Bedford Consulting Limited is a Cambridge-based consultancy specialising in clinical development and regulatory affairs services for companies developing biological pharmaceutical products and small molecules targeted for licensure in Europe and the United States of America. Services include:

  • Formulation of regulatory and clinical development strategy
  • Creation of product development plans
  • Preparation of regulatory and clinical documentation (including eCTD)
  • Advice and help with preparation for meetings with regulatory authorities
  • Project management from laboratory bench to product licence submission
  • Due diligence of business opportunities

Philip Bedford Consulting offers a unique blend of scientific knowledge with hands-on experience covering most aspects of the biopharmaceutical development process. The Company prides itself on providing a high-quality service in a flexible but timely manner.

Philip Bedford

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With more than 30 years of experience in both “blue chip” pharmaceutical and small cutting-edge biopharmaceutical companies, Philip Bedford has overseen the submission of 2 Biologics Licence Applications, 8 Investigational New Drug Applications and several EU Clinical Trial Applications.

In addition, he has managed more than 100 clinical trials from Phase 1 to 4. Scientific expertise includes, but is not limited to, vaccines, cell-based therapies, monoclonal antibodies and biological responses modifiers used in cancer, infectious disease, autoimmune disease, transplant rejection and wound care.

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