Pharmaceutical Current Good Manufacturing Practice (cGMP): Introductory Level

Dr. Kareim Hassanin

QC Manager

0 Instructor Rating 47 lectures 1 Courses 11112 Views
USD 15
Add to cart

Join our "Learn More & Save a life" initiative by buying this course & 50% from what you pay will go to buy Personal protective equipment for the medical staff

This course includes :

47 lectures 04:20:53 hours 0 Downloadable resources Full lifetime access Certificate of Completion In Arabic & English Updated at: 2024-12-22 04:22:12
USD 15

This course includes :

04:20:53 hours On-demand videos 0 Downloadable resources Full lifetime access Certificate of Completion In Arabic & English Updated at: 2024-12-22 04:22:12

You Will Learn

  • Quality Management and Pharmaceutical Quality System
  • cGMP requirements:
  • Quality Management
  • Sanitation and Hygiene
  • Qualification and Validation
  • Complaints and Recalls
  • Contract Production, Analysis, and Other Activities
  • Self-inspection and Quality Audits
  • Personnel
  • Premises
  • Equipment
  • Materials
  • Documentation

Description


Pharmaceutical Current Good Manufacturing Practice (cGMP): Introductory The level course covers the basic training for all employees working in pharmaceutical industry. It covers all the aspects of the industry as premises, personnel, equipment …

Accreditations


Upon completion of the  “Pharmaceutical Current Good Manufacturing Practice (cGMP): Introductory Level" course and successfully passing the exam, you will get a certificate approved by  the Arab Pharmacists Federation.


Pharmaceutical Current Good Manufacturing Practice (cGMP): Introductory Level

Some lectures will remain locked until you watch the previous ones.
Lec 1 Introduction
Lec 2 Quality Management Framework
Watch

02:20

Lec 3 Quality Management Requirements
Watch

04:29

Lec 4 Business Environment
Watch

04:40

Lec 5 Documentation
Watch

11:08

Lec 6 Introduction To cGMP
Watch

07:51

Lec 7 History Of cGMP
Watch

02:36

Lec 8 CGMP Regulations
Watch

02:41

Lec 9 Quality Relationships
Watch

02:44

Lec 10 Quality Assurance (Part 1)
Watch

03:03

Lec 11 Quality Assurance (Part 2)
Watch

06:15

Lec 12 Quality Risk Management (QRM)
Watch

04:57

Lec 13 cQRM Tools
Watch

02:41

Lec 14 Sanitation and Hygiene
Watch

02:19

Lec 15 Personal Hygiene
Watch

05:57

Lec 16 PPE
Watch

01:34

Lec 17 Premises Sanitation
Watch

03:18

Lec 18 Production Operations
Watch

02:46

Lec 19 Qualification and Validation (Part 1)
Watch

07:51

Lec 20 Qualification and Validation (Part 2)
Watch

03:13

Lec 21 Documentation
Watch

06:55

Lec 22 Phases Of Validation
Watch

02:18

Lec 23 Complaints Procedures
Watch

03:35

Lec 24 Defects and Root Cause Analysis
Watch

04:28

Lec 25 Product Recall
Watch

04:15

Lec 26 Production Contract (TOLL)
Watch

03:25

Lec 27 Contract
Watch

05:47

Lec 28 Responsibility Of The Contract Giver
Watch

03:18

Lec 29 Responsibility Of The Contract Acceptor
Watch

03:11

Lec 30 Self Inspection
Watch

09:27

Lec 31 Types Of Audit.
Watch

05:03

Lec 32 Self-Inspection Program
Watch

03:16

Lec 33 Personnel Requirements
Watch

06:18

Lec 34 Key Personnel
Watch

08:01

Lec 35 Responsibility Of Head Of Production and Quality Manager
Watch

07:41

Lec 36 Training
Watch

05:46

Lec 37 Premises
Watch

11:35

Lec 38 Specific Areas Requirements (Part 1)
Watch

07:34

Lec 39 Specific Areas Requirements (Part 2)
Watch

08:44

Lec 40 Equipment
Watch

07:26

Lec 41 Production Equipment
Watch

04:59

Lec 42 Material Requirements
Watch

04:45

Lec 43 Starting and Packaging Material
Watch

12:12

Lec 44 Bulk, Intermediate, and Finished Products
Watch

11:53

Lec 45 Documentation
Watch

08:27

Lec 46 Types Of Documentation (1). Master Formula
Watch

08:18

Lec 47 Types Of Documentation (2) Batch Records
Watch

07:49

Recommended courses
Reviews