Pharmacy and Poisons Regulations

	Cap 138A Empowering section Cap 138A Part 1 Preliminary Cap 138A reg 1 Citation Cap 138A reg 2 Interpretation Cap 138A reg 2A Poisons List Cap 138A reg 3 Application of section 22 restricted to Schedule 1 Cap 138A reg 4 Extension of labelling provisions and relaxation with respect to poisons in Schedule 6 Cap 138A reg 5 Extension of section 22 to sales wholesale etc. and relaxation of the section Cap 138A reg 6 Relaxation of section 28(3) in the case of certain medicines Cap 138A reg 7 Exemption from the provisions relating solely to Schedule 1 Cap 138A reg 8 Complete exemption for articles and substances in Schedule 2 Cap 138A Part 2 Additional Restrictions on the Sale of Poisons Cap 138A reg 9 Additional restriction of sale of poisons in Schedule 3 Cap 138A reg 10 Restriction of sales by listed sellers of poisons Cap 138A reg 10A Prohibition on dispensing of prescriptions by listed sellers of poisons Cap 138A reg 11 Restriction of sale of strychnine Cap 138A Part 3 Supplementary Provisions with respect to Labelling and Containers of Poisons* Cap 138A reg 12 Manner of labelling containers Cap 138A reg 13 Labelling of name of poison Cap 138A reg 14 Labelling of particulars as to proportions of the poison Cap 138A reg 15 "Poison" to be in English and Chinese Cap 138A reg 16 Special precautions in the case of certain articles Cap 138A reg 17 Name of seller and address of premises Cap 138A reg 18 Form of containers of poisons* Cap 138A Part 4 Storage and Transport of Poisons* Cap 138A reg 19 Storage of poisons Cap 138A reg 20 Transport of poisons Cap 138A reg 21 Special provisions with respect to the transport of poisons in Schedule 7 Cap 138A Part 5 Special Provisions with respect to Institutions Cap 138A reg 22 Supply of medicines to out-patients from certain institutions, etc. Cap 138A reg 23 Supply of medicines for use in institutions, etc. Cap 138A reg 24 Storage of poisons in institutions Cap 138A Part 5A Listed Sellers of Poisons Cap 138A reg 24A Applications to be entered on list under section 25 Cap 138A Part 5B Registration of Premises of Authorized Sellers of Poisons* Cap 138A reg 24B Applications to register premises under section 13 Cap 138A reg 24C (Repealed 2 of 2015 s. 44) Cap 138A Part 6 Wholesale Dealing in Poisons and Pharmaceutical Products* Cap 138A reg 25 Sale and supply of poisons or pharmaceutical products wholesale Cap 138A reg 26 Pharmacy and Poisons (Wholesale Licences) Committee Cap 138A reg 27 Sales of poisons by licensed wholesale dealers or licensed manufacturers* Cap 138A reg 28 Records to be kept by licensed wholesale dealers or licensed manufacturers* Cap 138A Part 7 Manufacture of Pharmaceutical Products* Cap 138A reg 28A Good Manufacturing Practice Guide Cap 138A reg 29 Licensing of manufacturers Cap 138A reg 30 Manufacture to be under supervision of a registered pharmacist Cap 138A reg 30A Authorized person to certify compliance with GMP Guide etc. Cap 138A reg 30B Register of authorized persons Cap 138A reg 30C Application for registration as authorized person Cap 138A reg 30D Registration as authorized person Cap 138A reg 30E Renewal of registration of authorized person Cap 138A reg 30F Cancellation or suspension etc. of registration as authorized person Cap 138A reg 31 Labelling by licensed manufacturers* Cap 138A reg 32 Manufacturing workers not to infect products Cap 138A reg 33 Duties of licensed manufacturers regarding identity, purity, safety, etc.* Cap 138A reg 34 Licensed manufacturer’s premises* Cap 138A reg 35 Records to be kept by licensed manufacturers* Cap 138A Part 8 Registration of Pharmaceutical Products and Substances Cap 138A reg 35A Interpretation (Part 8) Cap 138A reg 36 Registration of pharmaceutical products and substances Cap 138A reg 36A Application for approval to change the registered particulars of a registered product or substance Cap 138A reg 36B Clinical trials and medicinal tests Cap 138A reg 36C Definition of pharmaceutical product and substance for the purposes of this Part Cap 138A reg 36D Duplicate certificates Cap 138A reg 37 Factors relevant to determination of application for registration Cap 138A Part VIIIA (Repealed 2 of 2015 s. 61) Cap 138A reg 37A (Repealed 2 of 2015 s. 61) Cap 138A Part 9 Sale of Medicines Cap 138A reg 38 Disclosure of composition of medicines Cap 138A reg 38A Labelling of certain medicines Cap 138A Part 10 Miscellaneous Cap 138A reg 38B Power to specify forms Cap 138A reg 39 Period of keeping of records Cap 138A reg 40 Penalties Cap 138A reg 41 Certificates, forms and fees Cap 138A reg 42 (Omitted as spent—E.R. 3 of 2015) Cap 138A Sched 1 Substances to which Certain Restrictions with respect to the Sale, Supply, Labelling and Storage Apply under Regulations 3, 5, 6, 22 and 24* Cap 138A Sched 2 Articles Exempted by Regulation 8 from the Provisions of the Ordinance and of these Regulations Cap 138A Sched 3 Substances Required by Regulation 9 to be Sold by Retail only upon a Prescription Given by a Registered Medical Practitioner, Registered Dentist or Registered Veterinary Surgeon* Cap 138A Sched 4 Statement of Particulars as to Proportion of Poison in Certain Cases Permitted by Regulation 14(a) Cap 138A Sched 5 Indication of Statement Prescribed by Regulation 15 for the Purposes of Section 27(c) of the Ordinance Cap 138A Sched 6 Poisons Exempted by Regulation 4 from Labelling Provisions when Sold or Supplied in Certain Circumstances Cap 138A Sched 7 Poisons Required by Regulation 21 to be Specially Labelled for Transport Cap 138A Sched 8   Cap 138A Sched 9 Fees Cap 138A Sched 10 Poisons List

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