Hong Kong Regulations

PHARMACY AND POISONS REGULATIONS

- CHAPTER 138A

TABLE OF PROVISIONS

           Long Title

   1.      Citation
   2.      Interpretation
   3.      Application of section 22 restricted to the First Schedule
   4.      Extension of labelling provisions and relaxation with respect to
           poisons in the Sixth Schedule
   5.      Extension of section 22 to sales wholesale etc. and relaxation of
           the section
   6.      Relaxation of section 28(3) in the case of certain medicines
   7.      Exemption from the provisions relating solely to the First Schedule
   8.      Complete exemption for articles and substances in the Second Schedule
   9.      Additional restriction of sale of poisons in the Third Schedule
   10.     Restriction of sales by listed sellers of poisons
   10A.    Prohibition on dispensing of prescriptions by listed sellers of
           poisons
   11.     Restriction of sale of strychnine
   12.     Manner of labelling containers
   13.     Labelling of name of poison
   14.     Labelling of particulars as to proportions of the poison
   15.     "Poison" to be in English and Chinese
   16.     Special precautions in the case of certain articles
   17.     Name of seller and address of premises
   18.     Form of containers
   19.     Storage of poisons
   20.     Transport of poisons
   21.     Special provisions with respect to the transport of poisons in the
           Seventh Schedule
   22.     Supply of medicines to out-patients from certain institutions, etc.
   23.     Supply of medicines for use in institutions, etc.
   24.     Storage of poisons in institutions
   24A.    Applications to be entered on list under section 25
   24B.    Applications to register premises under section 13
   24C.    Certificate of registration under section 13
   25.     Sale and supply of poisons wholesale
   26.     Pharmacy and Poisons (Wholesale Licences) Committee
   27.     Sales by wholesale dealers
   28.     Records to be kept by wholesale dealer
   29.     Licensing of manufacturers
   30.     Manufacture to be under supervision of a registered pharmacist
   31.     Labelling by manufacturers
   32.     Manufacturing workers not to infect products
   33.     Duties of manufacturers
   34.     Manufacturer's premises
   35.     Records to be kept by manufacturers
   35A.    Interpretation (Part VIII)
   36.     Registration of pharmaceutical products and substances
   36A.    Application for approval to change the registered particulars of a
           registered product or substance
   36B.    Clinical trials and medicinal tests
   36C.    Definition of "pharmaceutical product" and "substance" for the
           purposes of this Part
   36D.    Duplicate certificates
   37.     Factors relevant to determination of application for registration
   37A.    Application for registration under section 28A
   38.     Disclosure of composition of medicines
   38A.    Labelling of certain medicines
   39.     Period of keeping of records
   40.     Penalties
   41.     Certificates, forms and fees
   42.     (Omitted as spent)
           SCHEDULE 1
           SCHEDULE 2
           SCHEDULE 3
           SCHEDULE 4
           SCHEDULE 5
           SCHEDULE 6
           SCHEDULE 7
           SCHEDULE 8
           SCHEDULE 9


[ Note: This table has been automatically generated and may be incomplete. ]