قواعد التصنيع الجيد للصناعات الدوائيه: المستوى التمهيدى

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