Consultant, Pharma Biotech

Email: pharmamail@nsf.org
Phone: +44(0)1751 432999
Country: United Kingdom

Paul Cummings has nearly 30 years’ experience in pharmaceutical R&D, specializing in parenteral product development in all its guises from product formulation development to due diligence activities, specialist auditing of parenteral facilities to cGMP, and design of parenteral manufacturing facilities.

He started his career working in a hospital pharmacy in the UK, and then moving into the pharmaceutical industry.  Mr. Cummings has worked on sites in Europe, America, Japan and Australia and he has a practical approach to each market’s requirements.  

Mr. Cummings’ recognized areas of expertise include:

  • R&D parenteral product development
  • Product formulations
  • Due diligence audits for R&D products
  • Design and practical applications of parenteral manufacturing facilities
  • Mentoring and coaching R&D professionals
  • Clinical trial manufacture
  • Pharmaceutical radiation safety
  • Regulatory submissions

He is also a Fellow of the Society of Biology.

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