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.

  • Chief/Sub Investigator

    Experience of being Chief/Sub Investigator for over 300 studies in all early phase drug development study designs including First in Human studies.

  • Subject safety

    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.

  • Data Interpretation

    Interpretation of data and its relevance to the development process.

  • Global Understanding

    Truly Global understanding of problems.

  • Dynamic

    Dynamic Working Approach.

  • Ethical

    High regard for the ethical conduct of research.

  • Regulatory Experience

    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.