Gain expertise in clinical trial processes, drug safety monitoring, and regulatory compliance.
Certification
RTMNU Certified
Level
Beginner
Duration
60 Hours (Online)
Modules
12 Modules
Assignments
10 Assignments
Students
1200+ Enrolled
Special Offer Price
₹2000
















To introduce students to clinical research processes
study designs
and protocols.
To develop knowledge of drug safety monitoring and pharmacovigilance principles.
To train students in regulatory compliance and ethical standards (ICH-GCP
FDA
CDSCO).
To provide practical understanding of adverse event reporting and risk management.
To prepare students for career opportunities in clinical research
pharma
and healthcare industries.
Understand clinical trial processes and phases.
Conduct adverse event monitoring and pharmacovigilance activities.
Ensure regulatory compliance and ethical practices in research.
Use basic clinical data management tools.
Pursue careers in clinical research organizations (CROs)
pharmaceutical companies
and healthcare monitoring agencies.
Career Paths
Roles
Diploma, Undergraduate and Graduate (Life Science, Pharmacy and Medical)
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Course Expert
Certified Trainer
| Features | Best Spruce | NPTL |
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Find answers to common questions about our courses, NEP 2020 compliance, and career opportunities.
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