An interview with the Pharmacy and Poisons Board (PPB) is a key review stage in the licence application process, particularly for the Person-in-Charge (RP) of a wholesaler licence and key personnel of a manufacturer licence. The main purpose of the interview is to assess whether the nominees genuinely have the professional knowledge and ability to supervise and manage medicine-related activities. Topics generally cover five core areas: 1) understanding of Hong Kong laws and regulations relating to medicines, such as the Pharmacy and Poisons Ordinance and the Import and Export Ordinance; 2) knowledge of Good Distribution Practice (GDP) or Good Manufacturing Practice (GMP); 3) ability to handle practical scenarios, such as managing a medicine recall, identifying and reporting counterfeit medicines, and managing the supply chain; 4) professional knowledge of the medicines covered by the application; and 5) personal responsibility and integrity.
HONG KONG DRUG LICENSING
What capabilities does the Pharmacy and Poisons Board (PPB) interview primarily assess in applicants?
A complete explanation of the regulatory basis, Drew Tang’s recommendations and risk alerts. The original material dates from 2025; read it alongside the latest official requirements.
Original guide, 2025 edition: These FAQs are provided for topic-based reference and have not all been individually checked against current rules. Please confirm fees, personnel, renewal, changes and product requirements against the professional in-depth guide for the relevant licence type and the official requirements in force at the time.
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