Dr Lisa Hinchliffe

LangAllan CMC Regulatory Solutions


Based in the UK, Lisa has around 20 years’ experience working in Regulatory CMC roles across Clinical Trials and Post-Licensing projects for a variety of leading global pharmaceutical organisations such as GSK, MSD, Novartis Vaccines and AZ, as well as working with a variety of smaller companies on large and small molecule projects. Lisa now runs her own limited company consultancy specialising in the CMC aspects of Regulatory submissions. Lisa is a Chartered Chemist and active Member of the Royal Society of Chemistry and the Joint Pharmaceutical Analysis Group. She holds a BSc Hons in Chemical and Pharmaceutical Sciences from the University of Sunderland and a PhD in pharmaceutical chemistry from the University of Derby.


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