David Fairlamb
Consultant
Clinical Research
AlacraMed
United Kingdom
Biography
David has more than 20 years of experience working within the drug and medical device industries, with much of this experience based on the regulation of borderline products (e.g. drug/device combination) and biotechnology developments. Prior to moving into consultancy, David held senior regulatory positions within Smith & Nephew, Seven Seas (Merck KGaA) and Renovo plc. In addition to regulatory positions, David has also held responsibility for medical writing functions, pharmacovigilance and as the clinical lead in regard to development and validation of clinical endpoints for novel therapeutic indications. David holds a Bachelor’s Degree in pharmacology, a post-graduate qualification in Regulatory Affairs and is a member of “The Organisation for Professionals in Regulatory Affairs” (TOPRA), and “Regulatory Affairs Professionals Society” (RAPS). David is also a registered Chartered Biologist with the UK Royal Society of Biology.
Research Interest
Clinical Research
