Dr David Jones

After spending 8 years in Contract Toxicology and 11 years as a Toxicologist in the Pharmaceutical Industry, David Jones currently work as an Expert Pharmaco-Toxicologist within the Licensing Division of the Medicines and Healthcare products Regulatory Agency (MHRA) in London.

His current role principally involves assessing nonclinical data for Clinical Trial Applications, both non-biological and biological.  A further aspect of his job is to offer regulatory advice to companies on behalf of  the MHRA or the EU’s Committee for Human Medicinal Products (CHMP).  David is one of the UK’s accredited non-clinical experts to support the CHMP and is the UK representative on the EU’s Safety Working Party (SWP). He represented the EU in the ICH revision of the M3 Guideline and is now on the new ICH S11 Guideline.

David is also a guest lecturer at the University of Surrey and the University of Wales and a frequent presenter at conferences around the world.