Our e-learning platform offers a wide range of modules covering essential topics in clinical research, including but not limited to
This course sets the foundations on understanding the requirements of ICH GCP and on how to successfully conduct a clinical trial according to internationally acceptable ethical, scientific and quality standards.
$69
A refresher will be provided on the following: Principles of GCP, Investigator, Sponsor and IRB/IEC responsibilities, Source Documents and Essential Documents, Informed Consent, Safety, Quality Management, Monitoring and IP management.
$49
This module will address the key fundamentals of managing a clinical study at the site. The Clinical Research Coordinators will be taken through the life cycle of a clinical study at the site and how to drive success of the clinical study.
$69
This module will introduce delegates to the fundamentals of research methodology that is key in the advancement of science and healthcare and management of patients.
$39
This module will provide on overview of the drug development process from identification of a potential molecule to the marketplace. An introduction to ICH GCP will also be provided.
$39
This module will provide an understanding of the essential components and structure of a scientifi publication. The IMRaD structure will be introduced as well as the requirements of the ICMJE for good scientific publications.
$49
Experience Learning Redefined
Expert-Led Courses:
Learn from leading professionals and researchers with real-world experience in clinical research.
Flexible Learning:
Access our modules anytime, anywhere, and at your own pace.
Interactive and Practical:
Engage with interactive content, practical exercises, and real-life case studies to enhance your learning experience.
Certification:
Earn certificates upon course completion to validate your expertise and advance your career.
