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Legislation Notes by Sharon Tang

Rated 5.00 out of 5 based on 1 customer rating
(1 customer review)

300.00$ Original price was: 300.00$.59.00$Current price is: 59.00$.

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Category: Uncategorized Tags: Legislation Notes, Legislation Notes by Sharon Tang, Sharon Tang
  • Description
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Description

Legislation Notes by Sharon Tang

Description

Your Instructor

 

Sharon Tang

Sharon Tang

Started this online tutorial platform in September 2017. I have a BPharm (1996) and a PhD in Pharmacognosy (2003) obtained from the University of London School of Pharmacy and have worked in community and in hospital in the UK. Since moving to Hong Kong several years ago I have passed the registration exams (2012). I have also taught pharmacology and human disease topics to pharmacy technicians and student nurses, which included writing exams and marking them. The Facebook group I run provides support for pharmacists taking the Hong Kong pharmacy registration exams.

Course Curriculum

 

Introduction
  •  
    Preview

    Introduction

Sections of the PPO and PPR – Cap 138 and 138A
  •  
    Preview

    Summary of the sections

ASPs, LSPs, and Basics of Poisons Categorisations (PPO)
  •  
    Preview

    Introduction – ASPs, LSPs, and Basics of Poisons Categorisations

  •  
    Start

    Medicines that can be kept in ASPs and LSPs

  •  
    Start

    Authorised Seller of Poisons (ASP) (S.11)

  •  
    Start

    Each premises is required to be under the control of a pharmacist (S.12)

  •  
    Start

    Registration of premises (S.13)

  •  
    Start

    Code of Practice for ASPs

  •  
    Start

    Display of Logo, and restriction on use of titles

  •  
    Start

    Listed Seller of Poisons (LSP) (S.25)

 

Labelling (PPO and PPR)
  •  
    Start

    Introduction

  •  
    Start

    Relevant sections of the Ordinance/Regs

  •  
    Start

    Labelling of Poisons (S.27)

  •  
    Start

    Exemptions for medicines (S.28)

  •  
    Start

    Extensions and relaxations (R.4)

  •  
    Start

    Supplementary Provisions for labelling (R.12-17)

  •  
    Start

    Transporting of poisons (R.21)

  •  
    Start

    Labelling requirements for manufacturers (R.31)

  •  
    Start

    Sale of medicines (R.38)

  •  
    Start

    Labelling of Part 2 and Non-Poisons (R.38A)

  •  
    Start

    PPB Code of Ethics – Mandatory labelling requirements for dispensed medicines

  •  
    Start

    Institutions (R.22,23)

  •  
    Start

    Dangerous Drugs (cap 134A)

Storage (PPR)
  •  
    Start

    Storage requirements (R.19)

Wholesale of Pharmaceutical Products (PPR)
  •  
    Start

    Wholesale – Relevant sections in the ordinance

  •  
    Start

    Definition

  •  
    Start

    Who can wholesale (R.25)

  •  
    Start

    Who wholesale dealers can sell to (R.27)

  •  
    Start

    Records (R.28)

  •  
    Start

    Recall system (R.28(8))

  •  
    Start

    Application for wholesale dealer license (R.26)

  •  
    Start

    Wholesale of Dangerous Drugs

  •  
    Start

    Code of Practice for Holder of Wholesale Dealer License

Manufacture (PPR)
  •  
    Start

    Manufacturing – Introduction and the GMP

  •  
    Start

    Licensing of manufacturers (R.29)

  •  
    Start

    Authorised Person (R.30A)

  •  
    Start

    Obligations and Duties

  •  
    Start

    Supervision (R.30)

  •  
    Start

    Health and hygiene of workers (R.32)

  •  
    Start

    Premises (R.34)

  •  
    Start

    Labelling (R.31)

  •  
    Start

    Quality Control and Recall System (R.33)

  •  
    Start

    Record keeping (R.35)

  •  
    Start

    Sale and supply (R.27)

  •  
    Start

    Dangerous drugs

  •  
    Start

    Definitions

Registration of pharmaceutical products and substances (PPR)
  •  
    Start

    Registration of products and substances – Introduction

  •  
    Start

    Registration of products and substances (R.36)

  •  
    Start

    Particulars to be registered (R.36A(3))

  •  
    Start

    Registration certificate (R.36(5))

  •  
    Start

    Clinical trials and medicinal tests (R.36B)

  •  
    Start

    Factors relevant to determination of applications (R.37)

Dangerous Drugs Ordinance and Regulations (DDO cap 134 and DDR 134A)
  •  
    Start

    Dangerous Drugs – Introduction

  •  
    Start

    Definitions

  •  
    Start

    The Dangerous Drugs List (Schedule 1)

  •  
    Start

    Example of forensic classification – Codeine

  •  
    Start

    Homework

  •  
    Start

    Trafficking (S.4)

  •  
    Start

    Supply (S.5)

  •  
    Start

    Import, Export, and Transit (S.10-21)

  •  
    Start

    Authority to procure, supply and possess (S.22-23)

  •  
    Start

    ASPs and LSPs (S.24)

  •  
    Start

    People who are allowed to possess DD (S.25)

  •  
    Start

    Supply of DD on prescription (S.31)

  •  
    Start

    Prescription requirements (R.3)

  •  
    Start

    Labelling (R.4)

  •  
    Start

    Record keeping (R.5-6)

Antibiotics Ordinance (Cap 137)
  •  
    Start

    Antibiotics Ordinance – Sections 1 & 2

  •  
    Start

    Section 3 – Substances to which the Antibiotics Ordinance applies

  •  
    Start

    Section 4 – Sale and Supply of Antibiotic Substances

  •  
    Start

    Section 4 – Administration of Antibiotics

  •  
    Start

    Section 4 – Prescription requirements

  •  
    Start

    Section 5 – Possession of Antibiotics

  •  
    Start

    Section 6 – Antibiotic permits

  •  
    Start

    Section 7 – Record keeping

  •  
    Start

    Schedule 8 – Notification that no scheduled antibiotics may be sold

  •  
    Start

    Section 9 – Inspections and enforcement of Ordinance

  •  
    Start

    Cap 137A – Antibiotics Regulations

Undesirable Medical Advertisements Ordinance (Cap 231)
  •  
    Start

    Undesirable Medical Advertisements Ordinance

  •  
    Start

    Definitions

  •  
    Start

    Prohibitions and Exceptions

  •  
    Start

    Schedule 1 – Prohibitions and exceptions continued

  •  
    Start

    Schedule 2 – Purposes for which it is prohibited to advertise any medicine, surgical appliance or treatment

  •  
    Start

    Responsibility

  •  
    Start

    Certain defences

  •  
    Start

    Prohibitions and Exceptions for Orally Consumed Products

  •  
    Start

    Penalty, power to amend, enforcement

 Frequently Asked Questions

When does the course start and finish?
The course starts now and never ends! It is a completely self-paced online course – you decide when you start and when you finish.
How long do I have access to the course?
How does lifetime access sound? After enrolling, you have unlimited access to this course for as long as you like – across any and all devices you own.
What if I am unhappy with the course?
We would never want you to be unhappy! If you are unsatisfied with your purchase, contact us in the first 30 days and we will give you a full refund.
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Reviews (1)

1 review for Legislation Notes by Sharon Tang

  1. Rated 5 out of 5

    tristian – May 25, 2020

    This is Digital Download service, the course is available at Coursecui.com and Email download delivery.

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