Paul R Palmer's profile and experience

Paul R Palmer has been in the pharmaceutical industry since 1986, he has accrued over 60,000 hours of experience in the development manufacture and supply of medicinal products and medical devices.

Throughout his career Paul has intentionally taken on all opportunities as they arose in order to develop a broad range of knowledge with an in-depth detailed understanding of manufacturing, storage, distribution, research, computerised systems, as well as the facilities and services to support each.

People and systems have always been a core focus, how to ensure best use optimise and enhance efficiency. Starting with biology has resulted in a level of curiosity rarely displayed in people taking on the qualified person role in pharmaceutical manufacturing. Culture, behaviour and psychology are all significant influences on the systems and processes we implement, but are often ignored.

Paul studied psychology as part of his MSc in 1993 and has always enjoyed observing the world around them with a curiosity that is rarely satisfied.

Working with Paul, you may find challenging as he pushes your systems and processes, further than you thought was possible.

Speciality skills

We support the Pharmaceutical Industry delivering their needs to ensure quality is assured.

Regulatory Inspection support ; preparation for, hosting of and resolution of observations. 100%
Pharmaceutical supplier auditing, Qualified Person declarations, oversight and qualification. 90%
Pharmaceutical Quality Management System ; review, optimisation and automation. 75%
Computer System Validation training, qualification and support. 55%
Training ; GMP, GDP, QP, RP, CSV, auditor whatever you need for your Pharmaceutical business we can deliver. 90%
Automation of systems and processes to enhance performance, efficiency and integration. 75%
Regulatory compliance advice and structure support when your organisation needs it. 55%