Both Online and OnCampus training is available
Good Clinical Practices training is used by thousands of institutions including many leading hospitals, academic medical centers, universities, and healthcare companies to meet their GCP training needs. Hence, experts in the Good Clinical Practices training sector are in high demand.
This training is designed for students to thrive in the Good Clinical Practices sector and focuses on various subjects such as GCP regulatory requirements, GCP in protocol development processes, GCP for Clinical Trials with Investigational Drugs and Medical Devices (U.S. FDA Focus), GCP for Clinical Trials with Investigational Drugs and Biologics (ICH Focus). The program also includes corresponding refresher courses for retraining and advanced learning.
Attendees may interact with the class and lead trainers for more clarifications or concerns.
Module 1
GCP regulatory requirements
GCP in clinical studies
Module 2
GCP in protocol development processes
GCP in various clinical study activities
GCP in clinical studies
Module 3
GCP for Clinical Trials with Investigational Drugs and Medical Devices (U.S. FDA Focus)
GCP for Clinical Trials with Investigational Drugs and Biologics (ICH Focus)
After successful completion of this course, students will be :
Anyone who wants to become the following should attend this webinar on good clinical practices:
Dr. Sanjida Ahmed joined NACPT in 2016, as Director of Strategic Planning & Business Development. She attained a Ph.D. in Cell Biology and Post Graduate Diploma in Clinical Research. Prior to her present position in NACPT and Validation Tech Inc., Dr. Ahmed worked as Director of Research & Business Development, in a Dubai based Biotechnology Company, Eastern Biotech & Life Sciences. She brings along 10 years of extensive experience in business development from the international market to stand out the growth of NACPT and Validation Tech.