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Here are all the products that are included in your bundle.
ALL COURSES
Proper documentation is essential for conducting high-quality research. In this course, participants will learn the requirements of good documentation practice and be equipped with the knowledge and skills needed to meet regulatory requirements.
$39
ALL COURSES
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
ALL COURSES
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
ALL COURSES
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
ALL COURSES
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
ALL COURSES
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