Harten Group

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Medical Affairs

With over 18 years' experience in supporting the Medical Affairs function in global pharmaceutical companies, Harten Group is ideally placed to provide specialist life sciences consultancy - from multi-disciplinary teams to individual specialists.

Providing Medico-marketing support, our Medical Affairs consultants are experienced in working in senior cross-functional roles, delivering time-critical clinical information for market launches and promotional campaigns, providing recommendations to Advisory Boards and advising on drug safety issues.

From our established network of 2000-plus consultants, over 600 are Medical Affairs specialists who, over recent years, have worked with 12 of the top 20 global pharma companies on hundreds of different projects. Some have provided help as part of a Medical Affairs team 'parachuted in' to offer complementary skills and experience; others have delivered specialist advice on an individual interim basis.

Our consultants are highly proficient in all elements of the Medical Affairs role copy approval including digital and web-based copy, keeping up-to-date with constantly changing regulations including the ABPI and PMCPA Codes to ensure compliance, supporting the pharmacovigilance function, accessing key opinion leaders and providing advice on clinical trials.

For a confidential discussion, please contact Dr Vernon Harten-Ash on +44 (0)1223 233777.

A very exciting opportunity in a new therapy area presented itself and we were keen to move quickly. Harten Group accessed a highly experienced specialist Medical Affairs team who delivered from day one, providing just the expertise we needed in terms of copy approval and PV advice

Medical Director, Top 10 US Pharma


Latest assignments

Phase I/II Physician

6 months, likely to extend

Medical Director / Clinical Science Director

6 months, likely to extend

Interim Medical Director

6 months, likely to extend

Recent projects & updates

A consultant has been helping a generics company headquartered in Ireland, currently branching into branded pharmaceuticals, with training and raising awareness of the Code to ensure local and UK compliance.

Harten Group consultant handles all regulatory requirements for compiling and submitting monthly safety updates for a global pharma company's antiviral during flu epidemic.

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