How to Manage Deviations in a GMP Environment – Part 2

Description:

This course has been designed to explain how to manage deviation in a regulated environment. By taking this course, you will learn how to identify deviations, how to train your personnel on deviation management, how to keep your deviations up-to-date,how to communicate all the necessary deviations with your colleagues and also How to close a deviation.

Curriculum for this course:
Introduction
Overview 1 min 10 secs
Learning objectives 1 min 13 secs
Who should take this course? 50 secs
Course modules 45 secs
Module 4: Deviation Archiving, Storage and Review
Definition archiving 1 min 23 secs
Step 1: Identify the types 1 min 52 secs
Step 2: Identify the information 58 secs
Step 3: Document the CAPA 1 min 30 secs
Definition archiving summary 1 min 15 secs
Deviation storage 1 min 23 secs
Storage space 1 min 19 secs
Storage method 1 min 22 secs
Storage conditions 48 secs
Deviation review 1 min 09 secs
System review and repetitive pattern analysis 1 min 33 secs
Trend and result analysis – Part 1 52 secs
Trend and result analysis – Part 2 1 min 10 secs
Strategic solution 1 min 45 secs
Management review 1 min 05 secs
Module 5: Deviation Closure
Steps for deviation closure 1 min 12 secs
Deviation closure documentation 1 min 20 secs
Bullet proof deviation prevention 45 secs
Module 6: Suggestion for Case Specific Deviation Handling
Industry deviations 1 min 29 secs
Sales and customer related deviations 1 min 17 secs
Service related 1 min 37 secs
Product related 1 min 07 secs
Module 7: Deviation Examples
Let’s set the scene 1 min 10 secs
Receiving the deviation 1 min 20 secs
Handling the deviation 1 min 33 secs
Corrective and preventative action 1 min 23 secs
Deviation communication 1 min 40 secs
Deviation closure 1 min 44 secs
Conclusion
Final Assessment
Certification
Author:

Start Learning Today!

We’ve got pricing plans to suit everyone

View Our Pricing Plans