RGYS organises Hong Kong drug licence, licensed-company acquisition and compliance resources, with related international service materials kept distinct.
The service directory below is organised by licence type. To compare the scope of business, application preparation, licensed operations and changes across the board, first read the comprehensive guide and then proceed to the relevant details. Further reading:ASP pharmacy, LSP dispensary, Western medicine wholesale, proprietary Chinese medicine wholesale
Supplying pharmaceutical products to pharmacies, hospitals and other authorised buyers, with a focus on the Person-in-Charge, compliant storage and a fully traceable distribution system.
View eligibility and application requirements ↗A pharmacy business serving the public, involving registered premises, supervision by a registered pharmacist, and statutory conditions governing the sale of medicines on prescription and under supervision.
View eligibility and application requirements ↗Suitable for retail sale of Part II poisons within the licensed scope. It cannot replace pharmacy authorisation, and Part I poisons may not be sold or restricted pharmacy signage used.
View eligibility and application requirements ↗Covers approved pharmaceutical product manufacturing activities, with a focus on PIC/S GMP, the quality system, premises and equipment, key personnel, and batch release.
View eligibility and application requirements ↗Plan the wholesale business in proprietary Chinese medicines under the separate regime established by Cap. 549. Check the business licence, product registration, labels and package inserts, imports and exports, and batch records separately; a wholesale licence does not replace other licences for Chinese medicine traders.
View eligibility and application requirements ↗Plan the transaction handover and ongoing operations around the licensed entity, genuine premises, key personnel and historical compliance record.
Acquisitions and shareholding changes ↗Learn separately about the competent authorities, application preparation, ongoing maintenance and change requirements for medicine retail, wholesale and manufacturing. Only country guides whose official sources and main text in seven languages have completed review are made available; all other entries are clearly marked as pending verification.
A comprehensive compilation of 137 professional guides and service materials across the 17 regional categories on the original site, for reference on company establishment, financial licences and related cross-border compliance matters.
The following are related service resources from the original Rengangyongsheng website. They are not a uniform guide to pharmaceutical licensing in every jurisdiction. A Hong Kong pharmaceutical licence cannot replace product registration, import or business licences in other jurisdictions; overseas projects must be assessed separately for the target market. The resources were written at different times, and actual services, quotations and rules should be verified on a case-by-case basis.
The links in this directory have been extracted in full from the original Hong Kong pharmaceutical licence guide by Rengangyongsheng. Service years, case numbers and partner claims in the original promotional material have not been presented as verified results for this website.
Read the additional content from the complete original text ↗Business Manager Tang Shangyong (Drew Tang) will review your products, operating model, licence type and preparation requirements with you one-to-one. The precise service scope is confirmed in writing; pharmaceutical duties are carried out by legally qualified personnel, and approvals are determined by the competent authorities.
