Tutorials > Course On Current Good Manufacturing Practices For Pharma

Course On Current Good Manufacturing Practices For Pharma

Date: 20 March 2023 | Posted by: voska89

Free Download Course On Current Good Manufacturing Practices For Pharma
Published 3/2023
MP4 | Video: h264, 1280x720 | Audio: AAC, 44.1 KHz
Language: English | Size: 10.07 GB | Duration: 17h 26m
Include Good practices in warehouse, analytical and, microbiology laboratory, data integrity and computerised system.

Free Download What you'll learn
Pharmacy,pharmaceuticals professionals
This course has been updated to include the advances in Current Good Manufacturing Practices. This is two-days course
This is very important training. Failure to learn GMP principles can loose product and production licences.
Everyone who is working in pharmaceutical should be trained on this course
Requirements
The person who is interested in learning should learn in focussed way to understand the concepts and practical approach.
Description
This course will help learners to understand good manufacturing practices. This course is prepared with special attention on good warehouse practices, good laboratory practices, good computerized systems, and good data integrity practices. Further, this course will discuss good documentation practices and good review practices also. Further emphasis will be Good behaviour practices are also considered while developing this course. As, Good behaviour will first be required to ensure data integrity and good manufacturing practices. This course will further specifically have lectures on data integrity aspects of analytical laboratories and microbiology laboratories.This course is having many lectures. Below different points will be discussed in the lecturesInvestigations, OOS, OOT in pharmaceuticals, stability study in pharmaceuticals, guideline expectations about different aspects of GMP, FDA citations, the computerized system compliance includes - FDA part 11, business continuity plan, and excel spreadsheet validation also.How you can be ready for inspection is also discussed with a special focus on computerized system requirements. Overall, this is the complete course for learning pharmaceuticals in all disciplines. This course contains many recorded lectures. Kindly request you fully focus on each lecture to understand it in a better way.Further, if you have any question/s, please put your questions in the comment section. I will respond to your questions.
Overview
Section 1: Good Warehouse Practices
Lecture 1 Introduction
Lecture 2 GMP in warehouse Part 1
Lecture 3 GMP in warehouser part II
Section 2: Good Laboratory Practices
Lecture 4 Good Behaviour Practices
Lecture 5 Stability Study
Lecture 6 OOS and OOT investigations
Lecture 7 Analytical method validation
Section 3: Data Integrity in Pharmaceuticals
Lecture 8 Data Integrity and audit trail review part 2
Lecture 9 Data Integrity in analytial laboratories
Lecture 10 Data Integrity in Microbiology Laboratories
Section 4: Good Documentation Practices
Lecture 11 Good Documentation Practices Vs data integrity
Lecture 12 Good Review Practices
Section 5: Good Computerised System/IT practices
Lecture 13 Excel Spreadsheet Validation
Lecture 14 Common Errors related to cGXP computerised system
Lecture 15 FDA part 11 compliance
Lecture 16 Business Continuity Plan
Pharmacy students, consultants, This course is essential for software vendors, auditors, and quality staff involved in GxP applications. • Regulatory Affairs • QA/ QC • IT/IS • Software Managers • Project Managers • Software vendors and suppliers

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