Good Clinical Practice (GCP) in Pharmaceuticals
Ensure ethical, compliant, and inspection-ready clinical trials aligned with global Good Clinical Practice standards.
This training program provides in-depth knowledge of Good Clinical Practice (GCP) guidelines applicable to clinical trials in the pharmaceutical industry. The course covers ethical principles, regulatory requirements, investigator responsibilities, sponsor oversight, documentation standards, and inspection readiness in accordance with ICH-GCP and global regulatory authorities. Participants will gain practical understanding to ensure subject safety, data integrity, and regulatory compliance in clinical research.
Course Content
Meet Your Instructor
Offered by Huksa, this L&D program is led by elite industry veterans—CXOs and Functional Heads with 25+ years of deep-domain expertise. You have the flexibility to customize the curriculum, select your preferred expert, and align the program to your organization’s specific objectives. Connect with the Huksa team to explore our array of top-tier trainers available for this course!
₹85,000.00
This course includes:
- Lessons 8
- Topics 32
- Duration 1 Day
- Quizzes 0
- Language English
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