Pui Man Leung
Independent Consultant in Pharmaceutical Medicine.
My years of experience in early phase Drug Development together with my experience in MHRA Clinical Trials Unit as Medical Assessor and widespread experience in acute hospital medicine & a deep understanding of Drug Safety are the mainstay of my strengths.
Wide clinical exposure
Wide clinical exposure in acute hospital medicine and over 14 years in the CRO industry in various different Phase 1 clinics and deep understanding in most therapeutic areas.
Wide ranging experience
Experience of working with the largest multinationals to the smallest virtual companies.
Experience of being Chief/Sub Investigator for over 300 studies in all early phase drug development study designs including First in Human studies.
Deep understanding of subject safety.
Drug development process
Ability to analyze individual problems and to understand the drug development process as well as the pharmacology.
Interpretation of data and its relevance to the development process.
Truly Global understanding of problems.
Dynamic Working Approach.
High regard for the ethical conduct of research.
Extensive experience of Regulatory Authority accreditation and clinical trial application processes through working in MHRA.
Training & Teaching
Extensive training/teaching experience and active involvement in Faculty of Pharmaceutical Medicine education, DPM examination and PMST training matters.