Drug Safety and Pharmacovigilance Training in Edison, NJ

• Blue-Green & Canary Deployments

• Chaos Engineering (Introduction)

• Serverless DevOps (AWS Lambda, Azure Functions)

We aim to build expertise in monitoring and assessing drug safety through:

• Mastery of adverse event reporting (including identifiable patient, reporter, suspect drug, and event).

• Proficiency in signal detection, risk mitigation, and regulatory frameworks.

• Skills to navigate pre- and post-marketing safety challenges using pharmacoepidemiology principles.

1. Monitor drug safety through adverse event collection, reporting, and analysis.

2. Apply signal detection methods to identify potential risks in real-world data.

3. Design risk management plans using assessment and mitigation strategies.

4. Navigate FDA GVP, EMA modules, and other regulatory frameworks.

5. Evaluate clinical trial safety data and post-marketing surveillance systems.

6. Master pharmacoepidemiology basics to interpret drug safety trends.

Program Name: Drug Safety and Pharmacovigilance Training

Duration: 6 Months (Flexible options available)

Mode: Online/In-person

Level: Beginner to Intermediate

Who Should Enroll?

• Pharmacovigilance professionals

• Clinical research associates

• Pharmacy/medical students

• Healthcare professionals