(GRACP) Global Regulatory Affairs Compliance Professional
Health care and Pharmaceutical
About Course
The GRACP course is a certification program for professionals who want to learn about the global regulatory affairs in the pharmaceutical, biotech, and medical device industries.
The course covers topics such as how to conduct clinical trials overseas, how to file compliant submissions with foreign regulators, and how to avoid common regulatory pitfalls in different regions.
Eligibilities
professionals who want to learn about global regulatory affairs in the pharmaceutical, biotech, and medical device industries.
To join this program and become certified, you need to: Choose three core courses from a list of topics such as FDA inspections, GCP, GLP, GMP, etc.
Choose one elective course from any course or from the core courses list.
Complete the courses within a three-year period. Pass the GRACP exam.
Note: Eligibility requirements may vary based on the specific course or program you choose. Please refer to the detailed course brochure for more information.
--- Health care and Pharmaceutical ---
(GRACP) Global Regulatory Affairs Compliance Professional
Total Days
26 Days
Total Hours
170 Hours
Your Achievement,
Recognized
Successfully complete the Global Regulatory Affairs Compliance Professional Program
and showcase your professional achievement with our certificate.
Certificate awarded upon successful completion of the program