PJC Pharma Consulting Ltd provides solutions to pharmaceutical issues across the globe

With over 150 combined years of experience in the pharmaceutical industry our senior consultants provide expertise on the development of small molecules, biologics, generic portfolio development, device development, new chemical entity and product line extension development, from candidate selection/concept to registration and commercial launch, human and veterinary pharmaceuticals.

PJC Pharma Consulting Ltd has worked with clients in the UK and Europe, USA, Canada, Switzerland, Bangladesh, India, Japan, Auistralia and Russia across a wide range of projects. 

The company is led by Paul Cummings, a Chartered Biologist, Fellow of the Society of Biology, Chartered Scientist and Fellow of the Royal Institute. The senior consultant team have expertise generated and honed over decades within numerous organisations around the world. These skills include GMP compliance, good documentation practise, QC, Development, Registration, Agency interactions, Due diligence and Cleaning Qualification and extractables and leachables, all to the latest cGMP expectations.

Our senior consultant team has hosted FDA meetings, FDA pre-approval inspections, MHRA, IMB, ANVISA, Japan Ministry of Health and Health Canada inspections. The team has many years of experience leading transnational groups based in Japan, EU, USA and Canada for development of products for World-wide markets.

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Whatever your pharmaceutical issue or training need, when you contact PJC Pharma Consulting Ltd you can be assured of a high quality, pragmatic solution.