Pharmaceutical Current Good Manufacturing Practice (cGMP): Introductory Level
قواعد التصنيع الجيد للصناعات الدوائيه: المستوى التمهيدى
USD
127
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
Created at: 2024-02-22 13:38:30
Updated at: 2025-02-23 00:59:29
Updated at: 2025-02-23 00:59:29
Pharmaceutical Current Good Manufacturing Practice (cGMP): Introductory Level
4:20:53
Lec 1 Introduction
02:04
Lec 2 Quality Management Framework
02:20
Lec 3 Quality Management Requirements
04:29
Lec 4 Business Environment
04:40
Lec 5 Documentation
11:08
Lec 6 Introduction To cGMP
07:51
Lec 7 History Of cGMP
02:36
Lec 8 CGMP Regulations
02:41
Lec 9 Quality Relationships
02:44
Lec 10 Quality Assurance (Part 1)
03:03
Lec 11 Quality Assurance (Part 2)
06:15
Lec 12 Quality Risk Management (QRM)
04:57
Lec 13 cQRM Tools
02:41
Lec 14 Sanitation and Hygiene
02:19
Lec 15 Personal Hygiene
05:57
Lec 16 PPE
01:34
Lec 17 Premises Sanitation
03:18
Lec 18 Production Operations
02:46
Lec 19 Qualification and Validation (Part 1)
07:51
Lec 20 Qualification and Validation (Part 2)
03:13
Lec 21 Documentation
06:55
Lec 22 Phases Of Validation
02:18
Lec 23 Complaints Procedures
03:35
Lec 24 Defects and Root Cause Analysis
04:28
Lec 25 Product Recall
04:15
Lec 26 Production Contract (TOLL)
03:25
Lec 27 Contract
05:47
Lec 28 Responsibility Of The Contract Giver
03:18
Lec 29 Responsibility Of The Contract Acceptor
03:11
Lec 30 Self Inspection
09:27
Lec 31 Types Of Audit.
05:03
Lec 32 Self-Inspection Program
03:16
Lec 33 Personnel Requirements
06:18
Lec 34 Key Personnel
08:01
Lec 35 Responsibility Of Head Of Production and Quality Manager
07:41
Lec 36 Training
05:46
Lec 37 Premises
11:35
Lec 38 Specific Areas Requirements (Part 1)
07:34
Lec 39 Specific Areas Requirements (Part 2)
08:44
Lec 40 Equipment
07:26
Lec 41 Production Equipment
04:59
Lec 42 Material Requirements
04:45
Lec 43 Starting and Packaging Material
12:12
Lec 44 Bulk, Intermediate, and Finished Products
11:53
Lec 45 Documentation
08:27
Lec 46 Types Of Documentation (1). Master Formula
08:18
Lec 47 Types Of Documentation (2) Batch Records
07:49
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