Our Training Programs
Industry-aligned 6-week intensive courses designed to launch your career in drug safety and clinical research.
Pharmacovigilance
Master Drug Safety Monitoring
Pharmacovigilance (PV) is the science of detecting, assessing, understanding, and preventing adverse effects of medicines. This course prepares you for roles in drug safety departments at pharma companies, CROs, and regulatory agencies.
Week-by-Week Curriculum
What You'll Learn
- 1Process ICSRs end-to-end
- 2Write medical narratives
- 3Use Argus Safety & ARISg
- 4Prepare PSUR/PBRER reports
- 5Understand MedDRA coding
- 6Pass PV interview rounds
Career Opportunities
Clinical Research
Drive Life-Saving Clinical Trials
Clinical Research is the backbone of drug development. This course covers the entire clinical trial lifecycle — from protocol design to regulatory submission — equipping you for roles at CROs, pharma companies, and research hospitals.
Week-by-Week Curriculum
What You'll Learn
- 1Understand full clinical trial lifecycle
- 2Apply ICH-GCP guidelines
- 3Conduct monitoring visits
- 4Manage protocol deviations
- 5Work with EDC systems
- 6Prepare regulatory submissions
Career Opportunities
Clinical Data Management
Ensure Data Integrity in Trials
Clinical Data Management (CDM) ensures the accuracy, completeness, and reliability of clinical trial data. This course trains you in database design, data cleaning, and regulatory compliance — skills in high demand at CROs and pharma companies.
Week-by-Week Curriculum
What You'll Learn
- 1Design and annotate CRFs
- 2Work with Medidata Rave & Oracle InForm
- 3Apply CDISC SDTM standards
- 4Manage data queries end-to-end
- 5Perform database lock procedures
- 6Understand 21 CFR Part 11
Career Opportunities
Ready to Start Your Career in Drug Safety?
Talk to our admissions team today. Batches fill up fast — secure your seat now.