Skip to main content
Business Licence Information Service
Mobile Version
Print
Business Licence Information Services
New Search
Medical Establishment - Medical Practitioner or Dentist, Private Practice
If your business involves the following situations, you may need to apply for specific licence(s). Please put a √ in the appropriate box(es) for further information:
You will conduct a clinical trial or medicinal test of proprietary Chinese medicines in Hong Kong.
You will import any radioactive substances or irradiating apparatus.
You will deal with controlled chemicals listed under Schedule 1, 2, or 3 to the Control of Chemical Ordinance, Cap. 145.
You will store or keep Schedule 1 or 2 controlled chemicals listed under the Control of Chemical Ordinance, Cap. 145.
You will export Schedule 1, 2 or 3 controlled chemicals listed under the Control of Chemicals Ordinance, Cap. 145.
You will import Schedule 1 or 2 controlled chemicals listed under the Control of Chemicals Ordinance, Cap. 145.
You will remove any Schedule 1 or 2 controlled chemicals listed under the Control of Chemicals Ordinance, Cap. 145 which are being transhipped.
You will dispose of or reprocess or re-cycle any chemical waste.
You will produce or cause chemical wastes to be produced (include storage, package, labelling and disposal).
You will, as a chemical waste producer, store chemical waste in any containers with a capacity exceeding 450 litres.
You will manufacture, produce, import, possess, use, sell or deal in/with radioactive substances.
You will manufacture, produce, import, possess, use, sell or deal in/with irradiating apparatus.
You will import any biological materials.
Your business entity will operate as a company with limited liability in Hong Kong.
Your company is incorporated outside Hong Kong and planning to establish a place of business in Hong Kong.
You will import any pharmaceutical products and medicines.
You will export any pharmaceutical products and medicines.
You will produce or cause to be produced any clinical waste, or have possession or custody of any clinical waste.
You will use your premises where you produce clinical waste to receive clinical waste that you generate in other premises or those delivered by other clinical waste producers.
You will commercialise regulated products (products made from human tissues that fall within the definition of regulated products under section 7A of the Human Organ Transplant Ordinance (Cap. 465)).
You will convey radioactive substances.
You will initiate, manage or conduct a clinical trial / medicinal test of drug.
You will import any pharmaceutical products and medicines containing dangerous drugs.
You will import any pharmaceutical products and medicines containing dangerous drugs.
You will export any pharmaceutical products and medicines containing dangerous drugs.
You will operate a day procedure centre providing scheduled medical procedures.