Novartis
Clinical Trials: Good Clinical Practice Specialization
Novartis

Clinical Trials: Good Clinical Practice Specialization

GCP Principles for Ethical Clinical Trials

Novartis Learning

Instructor: Novartis Learning

16,539 already enrolled

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Get in-depth knowledge of a subject
4.8

(613 reviews)

Beginner level
No prior experience required
4 weeks to complete
at 10 hours a week
Flexible schedule
Learn at your own pace
Get in-depth knowledge of a subject
4.8

(613 reviews)

Beginner level
No prior experience required
4 weeks to complete
at 10 hours a week
Flexible schedule
Learn at your own pace

What you'll learn

  • Explore the clinical trial process and the details of Good Clinical Practice principles.

Skills you'll gain

  • Category: Informed Consent
  • Category: Drug Development
  • Category: Clinical Research Coordination
  • Category: Clinical Research
  • Category: Document Management
  • Category: Electronic Medical Record
  • Category: Record Keeping
  • Category: Good Clinical Practices (GCP)
  • Category: Patient Education And Counseling
  • Category: Clinical Documentation
  • Category: Risk Management
  • Category: Clinical Data Management
  • Category: Regulatory Compliance
  • Category: Health Equity
  • Category: Patient Communication
  • Category: Clinical Research Ethics
  • Category: Clinical Trials
  • Category: Institutional Review Board (IRB)

Details to know

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Taught in English

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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: Good Clinical Practices (GCP)
Category: Informed Consent
Category: Drug Development
Category: Clinical Research
Category: Health Equity
Category: Patient Education And Counseling
Category: Institutional Review Board (IRB)
Category: Clinical Data Management
Category: Clinical Research Ethics
Category: Risk Management

What you'll learn

  • Explore the clinical trial process, the details of good clinical practice, and regulatory requirements.

Skills you'll gain

Category: Good Clinical Practices (GCP)
Category: Clinical Trials
Category: Clinical Research Ethics
Category: Institutional Review Board (IRB)
Category: Clinical Research Coordination
Category: Document Management
Category: Informed Consent
Category: Drug Development
Category: Electronic Medical Record
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: Good Clinical Practices (GCP)
Category: Clinical Documentation
Category: Informed Consent
Category: Clinical Trials
Category: Record Keeping
Category: Drug Development
Category: Clinical Research
Category: Patient Communication
Category: Institutional Review Board (IRB)
Category: Clinical Research Ethics
Category: Regulatory Compliance

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

Novartis Learning
Novartis Learning
Novartis
4 Courses27,112 learners

Offered by

Novartis

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