Pharmaceutical Current Good Manufacturing Practice (cGMP): Introductory Level

Dr. Kareim Hassanin

QC Manager

0 Instructor Rating 47 lectures 1 Courses 6209 Views
USD 39
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This course includes :

47 lectures 04:20:53 hours 0 Downloadable resources Full lifetime access Certificate of Completion In Arabic & English Updated at: 2022-09-24 21:59:51
USD 39

This course includes :

04:20:53 hours On-demand videos 0 Downloadable resources Full lifetime access Certificate of Completion In Arabic & English Updated at: 2022-09-24 21:59:51

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
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02:20

Lec 3 Quality Management Requirements
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04:29

Lec 4 Business Environment
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04:40

Lec 5 Documentation
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11:08

Lec 6 Introduction To cGMP
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07:51

Lec 7 History Of cGMP
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02:36

Lec 8 CGMP Regulations
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02:41

Lec 9 Quality Relationships
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02:44

Lec 10 Quality Assurance (Part 1)
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03:03

Lec 11 Quality Assurance (Part 2)
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06:15

Lec 12 Quality Risk Management (QRM)
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04:57

Lec 13 cQRM Tools
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02:41

Lec 14 Sanitation and Hygiene
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02:19

Lec 15 Personal Hygiene
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05:57

Lec 16 PPE
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01:34

Lec 17 Premises Sanitation
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03:18

Lec 18 Production Operations
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02:46

Lec 19 Qualification and Validation (Part 1)
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07:51

Lec 20 Qualification and Validation (Part 2)
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03:13

Lec 21 Documentation
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06:55

Lec 22 Phases Of Validation
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02:18

Lec 23 Complaints Procedures
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03:35

Lec 24 Defects and Root Cause Analysis
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04:28

Lec 25 Product Recall
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04:15

Lec 26 Production Contract (TOLL)
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03:25

Lec 27 Contract
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05:47

Lec 28 Responsibility Of The Contract Giver
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03:18

Lec 29 Responsibility Of The Contract Acceptor
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03:11

Lec 30 Self Inspection
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09:27

Lec 31 Types Of Audit.
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05:03

Lec 32 Self-Inspection Program
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03:16

Lec 33 Personnel Requirements
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06:18

Lec 34 Key Personnel
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08:01

Lec 35 Responsibility Of Head Of Production and Quality Manager
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07:41

Lec 36 Training
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05:46

Lec 37 Premises
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11:35

Lec 38 Specific Areas Requirements (Part 1)
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07:34

Lec 39 Specific Areas Requirements (Part 2)
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08:44

Lec 40 Equipment
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07:26

Lec 41 Production Equipment
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04:59

Lec 42 Material Requirements
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04:45

Lec 43 Starting and Packaging Material
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12:12

Lec 44 Bulk, Intermediate, and Finished Products
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11:53

Lec 45 Documentation
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08:27

Lec 46 Types Of Documentation (1). Master Formula
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08:18

Lec 47 Types Of Documentation (2) Batch Records
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07:49

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