cap 138a pharmacy and poisons regulations

cap 138a pharmacy and poisons regulations

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Home > Ordinance and Regulations > 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

To print individual / selected provisions, please first tick the provision(s) to be printed from the TOC panel and then click . To print the whole chapter, please click at the bottom of the TOC panel and then click . Please set the page orientation to Landscape for

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Pharmacy and Poisons Regulations (Cap. 138 sub. leg. A) Contents Regulation Page Part 1 Preliminary 1. Citation 1-2 2. Interpretation 1-2 2A. Poisons List 1-6 3. Application of section 22 restricted to the Schedule 1 1-6 4. Extension of labelling provisions and

Pharmacy and Poisons Regulations (Cap. 138A) Pharmacy and Poisons Regulations (Cap. 138A)

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Power to make regulations Cap 138 s 29A Power of Board to specify forms Cap 138 s 30 Pharmacy and Poisons Appeal Tribunal Cap 138 s 30A Right of appeal to Court of First Instance Cap 138 s 31 Poisons Committee Cap 138 s 32

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PHARMACY AND POISONS ORDINANCE RESOLUTION (Under section 29 of the Pharmacy and Poisons Ordinance (Cap. 138)) RESOLVED that the following Regulations, made by the Pharmacy and Poisons Board on 6 April 2009, be approved – (a) the

Power to make regulations Cap 138 s 29A Power of Board to specify forms Cap 138 s 30 Pharmacy and Poisons Appeal Tribunal Cap 138 s 30A Right of appeal to Court of First Instance Cap 138 s 31 Poisons Committee Cap 138 s 32

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PHARMACY AND POISONS ORDINANCE RESOLUTION (Under section 29 of the Pharmacy and Poisons Ordinance (Cap. 138)) RESOLVED that the following Regulations, made by the Pharmacy and Poisons Board on 6 April 2009, be approved – (a) the

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Cap 138A – PHARMACY AND POISONS REGULATIONS 1 Chapter: 138A PHARMACY AND POISONS REGULATIONS Gazette Number Version Date Empowering section 30/06/1997 (Cap 138, section 29) [1 July 1978] L.N. 145 of 1978 (Originally L.N. 163

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《2015年藥劑業及毒藥(修訂)條例》 2015年第2號條例 A136 條次 頁次 Pharmacy and Poisons (Amendment) Ordinance 2015 Ord. No. 2 of 2015 A137 Section Page 27. Section 32 amended (exemption在 with respect to sales wholesale and sales to certain

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requirements are offences under the Pharmacy and Poisons Ordinance and Regulations, of which the maximum penalty for each offence is a fine of $100,000 and two years’ imprisonment.

The Pharmacy and Poisons Board of Hong Kong (the Board) is established under section 3 of the Pharmacy and Poisons Ordinance (Cap. 138, Laws of Hong Kong) to carry out functions in accordance with the provisions of the said Ordinance and its subsidiary

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Pharmacy & Poisons Ordinance PPO, definition: “Pharmaceutical product” & “medicine” mean any substance or combination of substances – a) presented as having properties for treating or preventing disease in human beings or animals; or b) that may be used in

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Guidance Notes on Classification of Products as “Pharmaceutical Products” under the Pharmacy and Poisons Ordinance (Cap. 138) Preamble 1. According to the Pharmacy and Poisons Regulations (PPR)(Cap. 138A) a subsidiary legislation of the

Home > Ordinance and Regulations > Pharmacy and Poisons Regulations Cap 138A Empowering section Cap 138A Part I PRELIMINARY Cap 138A reg 1

This paper covers the following ordinances related to pharmacy practice in Hong Kong: Pharmacy and Poisons Ordinance Cap. 138A Pharmacy and Poisons Regulation Cap. 138A Poisons List Regulation Cap. 138B Pharmacy and Poisons (Pharmacy and Poisons

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Guidance Notes on Classification of Products as “Pharmaceutical Products” under the Pharmacy and Poisons Ordinance (Cap. 138) Preamble 1. According to the Pharmacy and Poisons Regulations (PPR)(Cap. 138A) a subsidiary legislation of the

Home > Ordinance and Regulations > Pharmacy and Poisons Regulations Cap 138A Empowering section Cap 138A Part I PRELIMINARY Cap 138A reg 1

This paper covers the following ordinances related to pharmacy practice in Hong Kong: Pharmacy and Poisons Ordinance Cap. 138A Pharmacy and Poisons Regulation Cap. 138A Poisons List Regulation Cap. 138B Pharmacy and Poisons (Pharmacy and Poisons

This Committee is established to carry out the following functions in accordance with the Pharmacy and Poisons Regulations (Cap.138A, Laws of Hong Kong) – (a) consider and approve applications for licence to manufacture pharmaceutical products, subject to

In accordance with regulation 26 Pharmacy and Poisons Regulations (Cap.138A, Laws of Hong Kong), the Pharmacy and Poisons (Wholesale Licences) Committee is established to: (a) to consider and approve applications for wholesale dealer licence, subject

The Pharmacy and Poisons (Listed Sellers of Poisons) Committee is established to consider and approve applications for listed sellers of poisons under regulation 24A of the Pharmacy and Poisons Regulations (Cap.138A, Laws of Hong Kong).

Poisons Committee Pharmacy Internship Training Committee Pharmacy and Poisons Ordinance Pharmacy and Poisons Regulations Poisons List Regulations Course of Training, Study and Examination for Applicants for Registration as Pharmacists Regulations

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[Rev. 2012] Pharmacy and Poisons CAP. 244 P15 – 3 [Issue 1] CHAPTER 244 PHARMACY AND POISONS ACT ARRANGEMENT OF SECTIONS PART I – PRELIMINARY Section 1. Short title. 2. Interpretation. 3. Establishment of Pharmacy and Poisons Board.

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PHARMACY AND POISONS BOARD OF HONG KONG Explanatory Notes on Registration as a Pharmacist I. GENERAL 1.1 Subject to the provisions of the Pharmacy and Poisons Ordinance, Cap. 138, any person who intends to practise as a pharmacist

New medicine labelling requirements to take effect from August 5, 2016 The provisions under the Pharmacy and Poisons Ordinance (Cap. 138) (the Ordinance) in relation to the labelling of medicines containing poisons with either “Prescription Drug 處方藥物” or

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Requirement of Elemental Impurities Levels/Limits in Registered Pharmaceutical Products Background Under the Pharmacy and Poisons Ordinance (Cap. 138) and its Regulations (Cap. 138A), pharmaceutical products should meet the criteria of safety, efficacy

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Requirement of Microbiological Quality of Registered Pharmaceutical Products in Non-sterile Dosage Forms Background Under the Pharmacy and Poisons Ordinance (Cap. 138) and its Regulations (Cap. 138A), pharmaceutical products should meet the criteria of

The Historical Laws of Hong Kong Online is a full-text image database providing access to past revised editions of Hong Kong Laws. The database comprises a total of seven consolidations of the laws of Hong Kong: 1890, 1901, 1912, 1923, 1937, 1950, and 1964

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Pharmacy and Poisons Act CAP. 28.32 Section 8 8 Registration of applicants When any person has applied to be registered and has proved to the satisfaction of the Minister — (a) that he has attained the age of 21 years; (b) that he is entitled to be registered by

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File Ref.: FHB/H/23/4 LEGISLATIVE COUNCIL BRIEF Pharmacy and Poisons Ordinance (Cap. 138) PHARMACY AND POISONS (AMENDMENT) REGULATION 2019 INTRODUCTION The Pharmacy and Poisons Regulations (“the Regulations”) (Cap. 138A) was

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PHARMACY AND POISONS ORDINANCE RESOLUTION (Under section 29 of the Pharmacy and Poisons Ordinance (Cap. 138)) RESOLVED that the following Regulations, made by the Pharmacy and Poisons Board on 29 September 2008, be approved – (a) the

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LAWS OF KENYA PHARMACY AND POISONS ACT CHAPTER 244 Revised Edition 2012 [1989] Published by the National Council for Law Reporting with the Authority of the Attorney [Rev. 2012] CAP. 244 Pharmacy and Poisons 3 [Issue 1] CHAPTER 244

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Pharmacy and Poisons Regulations CAP. 28.32.1 Regulation 1 2008 Revised Edition Page 5 PHARMACY AND POISONS REGULATIONS MADE UNDER SECTION 46 OF THE PHARMACY AND POISONS ACT1 1 Citation These Regulations may be cited as

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Bills Committee on Pharmacy and Poisons (Amendment) Bill 2014 Trade’s concerns towards the legislative proposals to enhance the regulation of pharmaceutical products in Hong Kong and the Administration’s responses At the meeting of the Bills Committee on

According to section 27 of the PPO, no person shall sell any poison unless the container is labelled in accordance with the Pharmacy and Poisons Regulations (Cap 138A) (PPR). Under the PPR, the container of a poison-containing pharmaceutical product must be clearly printed with both English and Chinese text as specified in Schedule 5 in respect of the kind of poison contained.