1

Section 3.1: Overview – Regulation of Pharmaceutical Products in Hong Kong

2

Assessment 3.1: Overview - Regulation of Pharmaceutical Products in Hong Kong

2 questions

3

Section 3.2: Regulation of Medical Device in Hong Kong and Greater Bay Area

4

Assessment 3.2: Regulation of Medical Device in Hong Kong and Greater Bay Area

2 questions

5

Section 3.3: Regulation of Health Supplements in Hong Kong

6

Assessment 3.3: Regulation of Health Supplements in Hong Kong

2 questions

7

Section 3.4: Great Bay Area Perspectives - Regulation of Pharmaceutical Products in China

8

Assessment 3.4: Great Bay Area Perspectives - Regulation of Pharmaceutical Products in China

3 questions

9

Section 3.5: Great Bay Area Perspectives - Regulation of Pharmaceutical Products in Macau

10

Assesment 3.5: Great Bay Area Perspectives - Regulation of Pharmaceutical Products in Macau

2 questions

11

Session 3.6: Pharmaceutical Advertisement - Local and Global Perspectives

12

Assessment 3.6: Pharmaceutical Advertisement - Local and Global Perspectives

2 questions

13

Session 3.7: Pharmaceutical Advertisement - Industrial Practice

14

Assessment 3.7: Pharmaceutical Advertisement - Industrial Practice

2 questions

15

Session 3.8: Understanding of Quality-related ICH Guidelines

16

Assessment 3.8: Understanding of Quality-related ICH Guideline

2 questions

17

Session 3.9: Overview of Common Technical Document Dossier

18

Assessment 3.9: Overview of Common Technical Document Dossier

2 questions