Master pharmacovigilance fundamentals: adverse events, ICSR workflows, MedDRA basics, databases, SOPs, SAE reconciliation, and real-world case handling. Includes GCP, GVP & HIPAA essentials and live Q&A.
“The DSAT webinar gave me clarity on adverse event reporting and SAE reconciliation. I updated my resume with new safety tasks and secured an interview with a CRO within two weeks.”
— Olivia M., Austin, USA“The focus on MedDRA coding, case processing, and safety database workflows helped me transition from a biology background into pharmacovigilance roles with confidence.”
— Noah P., Toronto, Canada“Step-by-step examples in Oracle Argus and regulatory compliance made PV tasks practical to understand. I now feel prepared to apply for Drug Safety Associate positions.”
— Aisha R., Hyderabad, IndiaClinical Operations & Pharmacovigilance Expert
Dr. Nate has 25+ years in clinical research and drug safety. He has led teams using CTMS/eTMF and safety systems such as Oracle Argus and Veeva, and applies RBM principles with strong regulatory rigor (ICH-GCP, GVP, HIPAA). His teaching style is practical and job-focused—expect real workflows, checklists, and interview-ready takeaways you can use immediately in DSA/ PV roles.