What you'll learn:
- What Good Clinical Practices Are?
- Guidelines of What An Ethical And Safe Trail Is?
- The Rights And Importance Of Consent Of The Trial Subjects
- The Duties Of The Sponsor And Investigator Of The Trial
- What Is International Council For Harmonization?
- Aims Of ICH
- How Was ICH Established?
- The Importance Of ICH
- Groups Working Within ICH
- ICH GCP E6 R2 Efficacy Guidelines
- Link Between ICH And GCP
- All About The Institutional Review Board, Investigators, Sponsors, Clinical Trial Protocol And Protocol Amendment, Investigator’s Brochure, Essential Documents
***Why this course is considered as a TOP RATED and BEST SELLING course for the ICH GCP category on Udemy?***
See what students are talking about in this course:
5***** Star Rating
I’m very glad I enrolled in this class! There’s so much information to be absorbed and she did a great job in presenting everything in as much detail as possible, but at the same time simplifying it to make your learning experience a lot smoother. This is a great course if you’re just starting out and want to know the fundamentals of GCP. This master class has it all!
---Devon Roman
5***** Star Rating
She is a great instructor, very transparent, cuts out all the BS getting straight to the meat and potatoes of the subject at hand, exactly how I like to learn.
I am happy about investing in this course. The videos are over the shoulder at the right pace explaining the process of understanding the clauses.
The course has left me feeling confident that I can achieve my goals, plus I had so much fun learning.
If you create any more courses, you have a repeat customer in me.
--- Rebecca
5***** Star Rating
Very well constructed course covering all the topics I was interested in. Really liked the step-by-step approach and tasks broken into manageable chunks, allowing me to absorb the information. The tutor was great, the notes were very helpful and I made a lot of use of the Quizzes and Assignments section.
Highly recommend the course for either a beginner or someone with some experience but a bit rusty (such as me).
--- Reshma
5***** Star Rating
She is an amazing teacher, the best I could find so far. She is knowledgeable, explains very well, has a nice and soothing voice, and has a great sense of presentation.
The course is also more hands-on than a lot of other courses where you practically just watch guys read. She explains clauses practically who ICH GCP E6 document.
If you want to learn and understand GCP or clinical research in general, this is a great place to start.
--- Varun P
5***** Star Rating
This is an excellent, cost-effective, and comprehensive course and I'm so glad to enroll in the class. Plus, I've learned so much from the basics that have been taught. I'm so grateful to have the instructor spending time to develop this course and share knowledge. Again, thanks, and this course is highly recommended!
--- Dennis Clayton
5***** Star Rating
The content was helpful and this was a nice quick review.
--- Ayesha A. Rizvi, Ed.D.
5***** Star Rating
The information is explained in a detailed manner
--- Monique Brown
5***** Star Rating
Bravo
--- Tshering JAMTSHO
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COMPLETE COURSE DESCRIPTION:
Welcome to the complete ICH Good Clinical Practices E6 R2 course.
In this course, we will learn what Good clinical practices are, guidelines of what an ethical and safe trial is, the rights and importance of consent of the trial subjects, the duties of the sponsor and investigator of the trial, and much more. Basically, I will walk you through the entire GCP guidelines document step by step.
My name is Warda Naz, and I will be leading you through this course.
Here at Magine Solutions highly experienced instructors, engineers, and doctors with more than 10 years of experience in the industry will guide you through very high-quality online courses.
At the end of the course, you will be able to understand
What is International Council for harmonization?
Aims of ICH
How was ICH established?
The importance of ICH.
Groups working within ICH
Efficacy Guidelines
What are Good clinical Practices (GCP)?
The link between ICH and GCP
All about the Institutional review board, investigators, sponsors, clinical trial protocol and protocol amendment, investigator’s brochure, essential documents for the conduct of a clinical trial, and much more.
We will also learn to understand these concepts by looking at case studies to strengthen the theoretical concepts.
The ideal student for this course is anyone who wants to learn about the ICH GCP E6 document or an existing professional who wants to expand on their current skills. There are no requirements necessary to enroll. I only ask to come open-minded and ready to learn.
Feel free to take a look at the course description and I look forward to seeing you inside. Thank you!!
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