Over 15 years of experience in regulation, including assessments of Medicines, vaccines, medical devices, diagnostics, and Emerging Technologies.
Regulatory Inspections, including Good Manufacturing Practice (GMP) and Good Clinical Practice (GCP) inspections, Market Surveillance, and Pharmacovigilance,

Technical areas of expertise include:

• Providing scientific and technical expertise on registration of Health Products;
• Reviewing scientific and regulatory assessments of Marketing Applications;
• Supporting reliance and joint review approaches;
• Advising on regulatory standards, guidelines, and best practices;
• Contributing to continental capacity strengthening;
• Supporting emergency regulatory preparedness where relevant