ICH-GCP:Good Clinical Practice(QUIZ+Guideline+Extra Lecture

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Monica Sharma

1:59:19

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1 - Introduction

1 - Institutional Review BoardIPR.html

1 - Introduction.mp4

01:58

2 - Pharma Regulatory Jargons.mp4

11:34

3 - DMF.mp4

07:32

4 - Audit.mp4

05:47

5 - Regulatory Compliance and Requirements.mp4

07:44

6 - Regulatory Regime India US and EU.mp4

07:49

7 - IPR Copyrights and Patents.mp4

17:54

8 - IPR in India.mp4

07:04

9 - IRB or IEC.mp4

04:53

2 - ICHGCP Principles Importance Link

2 - Question.html

10 - ICH GCP Preview.mp4

01:02

11 - ICHGCP Principles Importance Link.mp4

12:46

3 - ICH GCP E6 R2

3 - Multiple Choice Type Questions.html

12 - ICH GCP E6 R2 Guidelines.mp4

02:52

13 - Clause 21213.mp4

07:07

14 - Investigator Clause 4143.mp4

03:21

15 - Clause 4447.mp4

01:49

16 - Clause 48413.mp4

03:07

17 - Sponsor Clause 50510.mp4

07:44

18 - Sponsor Clause 511523.mp4

04:43

4 - Extra Lecture

19 - Quality Module 32 P2.mp4

02:33

Description

Unlocking ICH-GCP E6 R2: A Complete Guide to Good Clinical Practice in Clinical Research

What You'll Learn?

In the ICH GCP (International Council for Harmonisation - Good Clinical Practice) course, students will learn the essential principles and guidelines
for conducting clinical trials ethically and ensuring the safety and well-being of human participants.
They will gain a comprehensive understanding of the regulatory requirements, documentation, and standard operating procedures involved in the entire clinical tr
The course will cover topics like trial design, informed consent, data collection, monitoring, adverse event reporting, and quality assurance.
By completing the course, students will be equipped with the knowledge and skills necessary to adhere to GCP standards
contribute to successful and compliant clinical research.

Who is this for?

Clinical Research Organizations staff, students

Beginners

What You Need to Know?

Clinical Research Organizations staff, students

Beginners

More details

Description
Embark on a transformative journey through our comprehensive online course, "Mastering ICH-GCP E6 R2: Good Clinical Practice for Clinical Research." This meticulously crafted program is your gateway to becoming a proficient and certified expert in the intricacies of conducting ethical and high-quality clinical trials.
Designed for both novices and seasoned professionals, this course delves deep into the International Conference on Harmonization (ICH) guidelines, specifically E6 R2, elucidating every facet of Good Clinical Practice (GCP) in the realm of clinical research. With a dynamic blend of engaging multimedia content, interactive modules, and real-world case studies, you'll gain an in-depth understanding of the core principles of ICH-GCP E6 R2, ensuring the highest standards of participant safety, data integrity, and ethical conduct.
Our industry-renowned instructors, each a luminary in their respective fields, will guide you through essential topics such as obtaining informed consent, protocol adherence, adverse event reporting, and investigator responsibilities. Additionally, you'll explore the critical role of Institutional Review Boards (IRBs) and gain practical insights into effective monitoring techniques.
Upon successful completion, you'll not only be armed with a comprehensive knowledge of ICH-GCP E6 R2 but also earn a prestigious certification that solidifies your expertise and enhances your career prospects in the dynamic landscape of clinical research. Join us today and unlock the doors to excellence in Good Clinical Practice. Your journey toward mastering ICH-GCP E6 R2 starts here.
Who this course is for:
Clinical Research Organizations staff, students
Beginners

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