Advances in GMP for Pharmaceuticals

Advances in GMP for Pharmaceuticals, available at $44.99, has an average rating of 4.1, with 16 lectures, based on 23 reviews, and has 108 subscribers.

You will learn about 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 This course is ideal for individuals who are 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 It is particularly useful for 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.

Enroll now: Advances in GMP for Pharmaceuticals

Summary

Title: Advances in GMP for Pharmaceuticals

Price: $44.99

Average Rating: 4.1

Number of Lectures: 16

Number of Published Lectures: 16

Number of Curriculum Items: 16

Number of Published Curriculum Objects: 16

Original Price: ₹1,499

Quality Status: approved

Status: Live

What You Will 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

Who Should Attend

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

Target Audiences

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

This course will help learners to understand advanced 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 on Good behavior practices are also considered while developing this course. As Good behavior 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 has many lectures. Below different points will be discussed in the lectures

Investigations, 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.

Course Curriculum

Chapter 1: Good Warehouse Practices

Lecture 1: Introduction

Lecture 2: GMP in warehouse Part 1

Lecture 3: GMP in warehouser part II

Chapter 2: Good Laboratory Practices

Lecture 1: Good Behaviour Practices

Lecture 2: Stability Study

Lecture 3: OOS and OOT investigations

Lecture 4: Analytical method validation

Chapter 3: Data Integrity in Pharmaceuticals

Lecture 1: Data Integrity and audit trail review part 2

Lecture 2: Data Integrity in analytial laboratories

Lecture 3: Data Integrity in Microbiology Laboratories

Chapter 4: Good Documentation Practices

Lecture 1: Good Documentation Practices Vs data integrity

Lecture 2: Good Review Practices

Chapter 5: Good Computerised System/IT practices

Lecture 1: Excel Spreadsheet Validation

Lecture 2: Common Errors related to cGXP computerised system

Lecture 3: FDA part 11 compliance

Lecture 4: Business Continuity Plan

Instructors

Hitendrakumar Shah
Pharmaceutical cGMP Compliance Consultant, Trainer & Auditor

Rating Distribution

1 stars: 1 votes
2 stars: 0 votes
3 stars: 3 votes
4 stars: 4 votes
5 stars: 15 votes

Frequently Asked Questions

How long do I have access to the course materials?

You can view and review the lecture materials indefinitely, like an on-demand channel.

Can I take my courses with me wherever I go?

Definitely! If you have an internet connection, courses on Udemy are available on any device at any time. If you don’t have an internet connection, some instructors also let their students download course lectures. That’s up to the instructor though, so make sure you get on their good side!

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