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Pharmaceutical Medicine

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Nature of the work

Pharmaceutical medicine is concerned with the discovery, development, evaluation, registration, monitoring and medical aspects of the marketing of medicines.

Working in pharmaceutical medicine

Careers in pharmaceutical medicine relate to three main groups of physicians:

  • those working in the pharmaceutical industry
  • those with appointments within medicines regulatory bodies (such as the MHRA)
  • those working in independent clinical research organisations dedicated to the development of new medicines.

A pharmaceutical physician may be responsible (alongside his or her team) for the clinical development of one or more compounds, and the effective evaluation of associated benefits and risks. This can represent a major challenge in a discipline which is by definition always working on the frontiers of science.

The specialty is now evolving rapidly after a slow gestation. There is increased recognition of the discipline of pharmaceutical medicine in many countries around the world, and formal recognition in UK, Ireland, Switzerland and Mexico. There are many postgraduate training programmes, particularly in Europe, leading to a Diploma in Pharmaceutical Medicine or a master’s degree, with or without subsequent accreditation of the qualification.

The role of the pharmaceutical physician has widened to cover all areas of pharmaceutical medicine, including:

  • drug candidate selection
  • clinical research
  • medical marketing
  • drug safety and pharmacovigilance
  • regulatory affairs
  • medical and scientific affairs
  • pharmacoeconomics
  • societal and public health issues relating to pharmaceuticals in the wider context of healthcare delivery.

Common procedures / interventions

These include:

  • planning, organisation, analysis and reporting of clinical trials on medicines
  • collecting, assessing and regulatory reporting of suspected adverse drug reactions
  • the preparation of product information such as an investigator’s brochure, a summary of product characteristics or patient information leaflets
  • ensuring promotional material complies with relevant pharmaceutical industry codes of practice
  • preparation of reports such as safety summaries and periodic safety update reports.

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