Good Clinical Practice (GCP)
Key features of the GCP guideline, roles and responsibilities involved and the requirements of essential documentation.
Ratings 4.42 / 5.00
What You Will Learn!
- Understand the global standard, and key variations in specific countries (eg, China)
- Learn when and where you want, with the flexibility of online learning
- Learn more effectively with video lecture capture
- Choose between lectures delivered in English or Chinese
- The topics cover ICH and SFDA standards
- Integrate with corporate learning management systems via SCORM compliance
Description
The principles of Good Clinical Practice (GCP) underpin the legal requirements for the conduct of clinical trials around the world. Originally developed as a unified standard by the European Union (EU), Japan and the United States (US), it also forms the basis of national regulation in many other countries, including China, India, Korea and Brazil.
A strong understanding of GCP is a fundamental requirement for anyone intending to develop a career in any aspect of clinical research, whether in industry, healthcare provision or academia.
This course introduces GCP for new professionals, but also serves as a refresher for those who feel they need it. The programme is clear and simple in design and gives full instructions for use.
Multi user pricing options are available. Contact us for more information.
Who Should Attend!
- This course introduces GCP for new professionals, but also serves as a refresher for those who feel they need it.
