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Course / Course Details

Pharmaceutical GMP Auditor

  • Rajashri Ojha image

    By - Rajashri Ojha

  • 0 students
  • 3 Hours
  • (0)

Course Requirements

B.Pharm/M.Pharm/PhD/BSc/MSc/
B.Tech/M.Tech/Pharma, Healthcare Working Professionals.

Course Curriculum

  • 10 chapters
  • 108 lectures
  • 0 quizzes
  • 3 Hours total length
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1 Introduction
15 Min


2 GMP articles and guidance 1
15 Min


3 GMP articles and guidance 2
15 Min


4 PPT 1
15 Min


5 PPT 2
15 Min


6 GMP video 1
1 Min


7 GMP video 2
1 Min


8 Good Documentation practice Video
1 Min


9 Good Documentation Practice Video - documents and records
1 Min


10 Good Documentation Practice Video - importance of documentation
1 Min


11 Good Documentation Practice Video - process of document
1 Min


12 Good Documentation Practice Video - data integrity
1 Min


13 GMP Lecture Video 1
1 Min


14 GMP Lecture Video 2
1 Min


1 Introduction
15 Min


2 Article guidance
15 Min


3 GxP PPT
15 Min


4 GxP Video 1
1 Min


5 GxP Video 2
1 Min


1 Introduction
15 Min


2 PPT 1
15 Min


3 PPT 2
15 Min


4 Article and Guidances
15 Min


5 Video ISO 9001: 2015
1 Min


6 The Requirements of GMP video 1
1 Min


7 The Requirements of GMP video 2
1 Min


8 The Requirements of GMP video 3
1 Min


9 The Requirements of GMP video 4
1 Min


10 The Requirements of GMP video 5
1 Min


1 Audit and Audit preparation
15 Min


2 PPT - How to successfully face an audit
15 Min


3 PPT - Audit Overview
15 Min


4 PPT - Role of an auditor
15 Min


5 PPT - Audit Readiness
15 Min


6 PPT - Audit Process based QMS
15 Min


7 Articles and Guidances 1
15 Min


8 Articles and Guidances 2
15 Min


9 Video-Auditing
1 Min


10 Video-Do and Don't - part1
1 Min


11 Video- Inspection Readiness
1 Min


1 Introduction
15 Min


2 Article and Guidance - 1
15 Min


3 Article and Guidance - 2
15 Min


4 Article and Guidance - 3
15 Min


5 Article and Guidance - 4
15 Min


6 PPT 1
15 Min


7 PPT 2
15 Min


8 Deviations, Root Cause Analysis tool and CAPA video
1 Min


9 Auditing Video 1
1 Min


10 Auditing Video 2
1 Min


1 ICH Q7, Q8, Q9, Q10 and their role in Pharmaceutical Industry
15 Min


2 Articles and Guidance 1
15 Min


3 Articles and Guidance 2
15 Min


4 Articles and Guidance 3
15 Min


5 Articles and Guidance 4
15 Min


6 ICH Q 10 video
1 Min


7 ICH Q 9 video
1 Min


8 ICH Q 8 video
1 Min


1 Chapter 7: ISO 19011: 2018 and 21 CFR part 11
15 Min


2 Articles and Guidance 1
15 Min


3 Articles and Guidance 2
15 Min


4 Articles and Guidance 3
15 Min


5 Articles and Guidance 4
15 Min


6 Articles and Guidance 5
15 Min


7 PPT 1
15 Min


8 PPT 2
15 Min


9 Computerized GxP Validation Video 1
1 Min


10 Computerized GxP Validation Video 2
1 Min


11 21 CFR part 11 video
1 Min


12 ISO 19011: 2018 Video 1
1 Min


13 ISO 19011: 2018 Video 2
1 Min


14 ISO 19011: 2018 Video 3
1 Min


15 ISO 19011: 2018 Video 4
1 Min


1 Introduction
15 Min


2 PPT 1
15 Min


3 PPT 2
15 Min


4 PPT 3
15 Min


5 Articles and Guidance 1
15 Min


6 Articles and Guidance 2
15 Min


7 Remote Auditing Video
1 Min


1 Good Manufacturing Practices and its Regulations (International perspective)
15 Min


2 PPT
15 Min


3 Articles and Guidance 1
15 Min


4 Articles and Guidance 2
15 Min


5 Articles and Guidance 3
15 Min


6 Articles and Guidance 4
15 Min


7 GMP video 1
1 Min


8 GMP video 2
1 Min


9 GMP video 3
1 Min


1 Computer System Validation and GAMP5
15 Min


2 PPT 1
15 Min


3 PPT 2
15 Min


4 PPT 3
15 Min


5 PPT 4
15 Min


6 Articles and Guidances 1
15 Min


7 Articles and Guidances 2
15 Min


8 Articles and Guidances 3
15 Min


9 Articles and Guidances 4
15 Min


10 Articles and Guidances 5
15 Min


11 Articles and Guidances 6
15 Min


12 Articles and Guidances 7
15 Min


13 Articles and Guidances 8
15 Min


14 Articles and Guidances 9
15 Min


15 Articles and Guidances 10
15 Min


16 Importance of CSV video 1
1 Min


17 Importance of CSV video 2
1 Min


18 Importance of CSV video 3
1 Min


19 GAMP in Pharma Industry video
1 Min


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