Our course series on ICH Good Clinical Practice equips trial investigators and clinical researchers with the essential knowledge required to conduct reliable and ethical clinical trials. Whether you are new to the field or an experienced professional, this course series provides the background needed to ensure participant safety, data integrity, and compliance with international regulations.
Clinical Trials: Good Clinical Practice Specialization
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Clinical Trials: Good Clinical Practice Specialization
GCP Principles for Ethical Clinical Trials
Instructor: Novartis Learning
13,618 already enrolled
Included with 
Get in-depth knowledge of a subject
(543 reviews)
Beginner level
No prior experience required
1 month at 10 hours a week
Flexible schedule
Earn a career credential
Share your expertise with employers
Get in-depth knowledge of a subject
(543 reviews)
Beginner level
No prior experience required
1 month at 10 hours a week
Flexible schedule
Earn a career credential
Share your expertise with employers
What you'll learn
Explore the clinical trial process and the details of Good Clinical Practice principles.
Overview
What’s included
Shareable certificate
Add to your LinkedIn profile
Taught in English
26 practice exercises
Advance your subject-matter expertise
- Learn in-demand skills from university and industry experts
- Master a subject or tool with hands-on projects
- Develop a deep understanding of key concepts
- Earn a career certificate from Novartis
Specialization - 3 course series
What you'll learn
Explore the clinical trial process, the basics of good clinical practice, and the history of regulatory frameworks for medical treatment and testing.
Skills you'll gain
Category: Clinical Trials
Category: Regulatory Compliance
Category: Clinical Research
Category: Risk Management
Category: Patient Education And Counseling
Category: Medical Science and Research
Category: Healthcare Ethics
Category: Medical Privacy
What you'll learn
Explore the clinical trial process, the details of good clinical practice, and regulatory requirements.
Skills you'll gain
Category: Clinical Trials
Category: Record Keeping
Category: Medical Science and Research
Category: Regulatory Compliance
Category: Healthcare Ethics
Category: Document Management
Category: Risk Management
Category: Clinical Research
What you'll learn
Explore the clinical trial process, the details of good clinical practice, and regulatory requirements.
Skills you'll gain
Category: Clinical Trials
Category: Record Keeping
Category: Regulatory Compliance
Category: Patient Safety
Category: Patient Education And Counseling
Category: Healthcare Ethics
Category: Clinical Research
Earn a career certificate
Add this credential to your LinkedIn profile, resume, or CV. Share it on social media and in your performance review.
Instructor
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Frequently asked questions
This course is completely online, so there’s no need to show up to a classroom in person. You can access your lectures, readings and assignments anytime and anywhere via the web or your mobile device.
If you subscribed, you get a 7-day free trial during which you can cancel at no penalty. After that, we don’t give refunds, but you can cancel your subscription at any time. See our full refund policy.
Yes! To get started, click the course card that interests you and enroll. You can enroll and complete the course to earn a shareable certificate. When you subscribe to a course that is part of a Specialization, you’re automatically subscribed to the full Specialization. Visit your learner dashboard to track your progress.
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Financial aid available,