This course is part of the "GCP Mutual Recognition Program" and is therefore accredited by TransCelerate BioPharma Inc. The Patronage of Transcelerate aims to standardize the GCP training for Research Teams and ensures that your chosen course meets the basic requirements for the GCP course.
The Transcelerate program is recognizable and accepted by pharmaceutical companies around the world.
Courses:
GCP Training
- After finishing this course, you will acquire knowledge in the following areas:
- • Principles of Good Clinical Practice
- • Role of Regulatory Bodies
- • Responsibilities of the Sponsor and Investigator
- • Basics of maintaining source documentation
- • Informed Consent Process
- • Monitoring of Clinical Trials
- • Safety Reporting
- The course is completed with a test consisting of 15 questions. Gaining 80% correct answers in final test generates a certificate valid for 2 years.
Clinical trials: principles, documentation, legal aspects
- Training for students and university staff covering all necessary clinical trial information.
- Training is conducted at higher education institutions.
- This training is the absolute basis for understanding the definitions used in clinical trials.
- Available only in Polish language version
If you wish to take the course, please contact us at office@clinicalconsulting.pl.
Cooperating Universities
