Get industry‑ready for pharma and life sciences.
Live online training in drug safety, medical writing and regulatory work.
Choose your program
Already in pharma or life sciences?
Sharpen your skills in pharmacovigilance, safety writing and regulatory work, and move up.
Starting your career?
Graduates in pharmacy, medicine and life sciences: learn the workflows employers expect on day one.
Pharmacovigilance
Understanding drug safety. Protecting patients.
- Duration
- 20 hours
- Schedule
- 10 sessions of 2 hours
- Format
- Live online
Develop foundational and applied knowledge of pharmacovigilance processes, safety reporting, and regulatory expectations.
What you'll learn
- Pharmacovigilance principles and regulatory frameworks
- Adverse event reporting and ICSR processing
- Drug safety surveillance and documentation
- Case assessment, quality, and compliance
- Real-world pharmacovigilance workflows
Medical writing
Turning science into clear, credible communication.
- Duration
- 24 hours
- Schedule
- 12 sessions of 2 hours
- Format
- Live online
Strengthen your ability to interpret scientific evidence and develop accurate, structured medical and regulatory documents.
What you'll learn
- Scientific and regulatory medical writing
- Literature review and evidence interpretation
- Clinical and scientific documentation
- Research manuscripts and publications
- Writing quality, accuracy, and compliance
Signal management
From safety data to informed decisions.
- Duration
- 8 hours
- Schedule
- 8 sessions of 1 hour
- Format
- Live online
Understand how emerging drug safety concerns are identified, evaluated, and managed within pharmaceutical safety systems.
What you'll learn
- Signal detection and identification
- Signal validation and prioritization
- Safety data evaluation
- Signal assessment and documentation
- Practical exercises and case-based learning
Risk management plans
Understanding risks. Strengthening medicine safety.
- Duration
- 6 hours
- Schedule
- 6 sessions of 1 hour
- Format
- Live online
Explore the scientific and regulatory considerations involved in developing and maintaining effective risk management plans.
What you'll learn
- Principles of pharmaceutical risk management
- Identification and characterization of safety concerns
- Risk minimization measures
- Regulatory expectations for RMPs
- RMP structure, preparation, and review
Aggregate safety report authoring
Transforming safety evidence into regulatory reports.
- Duration
- 10 hours
- Schedule
- 10 sessions of 1 hour
- Format
- Live online
Develop an understanding of aggregate safety reporting, scientific evaluation, and the preparation of structured regulatory safety documents.
What you'll learn
- Aggregate safety reporting principles
- PSUR/PBRER and DSUR fundamentals
- Safety data collection and interpretation
- Benefit–risk evaluation
- Report authoring, structure, and quality review
How it works
Message us on WhatsApp
Tell us which program interests you.
Pick your batch
We share dates, timings and fees.
Attend live sessions
Online, with real-world exercises.
Apply it at work
Leave with skills you can use on the job.
Ready to take the next step in your career?
Talk to us about the right program for you.