Richard Taylor is Head of
Regulatory Affairs for Veeda
Clinical Research and is responsible
for providing regulatory solutions
to support our clients’ product
development programs and providing
on-going regulatory support once
products are registered.
Formerly Head of International Clinical & Regulatory Affairs with Zeneca Pharma International, (now part of AstraZeneca plc), Dr Taylor was responsible for the strategic development of clinical trials and regulatory affairs capability for Central and South America, Middle East and Africa, Asia Pacific and Central and Eastern Europe.
Previously, Dr. Taylor held management positions with Fisons Pharmaceuticals (now part of Aventis) and The Wellcome Research Laboratories (now part of GlaxoSmithKline plc), where he was Head of OTC medicines in International Medical Affairs.
Richard Taylor is an assessor for
The Royal College of General
Practitioners Primary Care Research
Team, which assists UK physicians’
practices gain accreditation to
conduct clinical studies. He is a recipient
of a Medical Research Council
Scholarship at The Institute of
Psychiatry and Kings College
Hospital Medical School, London, UK,
and holder of the first UK College
of Pharmacy Practice Research
Fellowship.
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