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Virtual

Apr 14, 2026 9:00 AM - Apr 16, 2026 1:00 PM

(Central Europe Standard Time)

Understanding Pharmacoepidemiology and Real-World Evidence Studies

NEW OFFERING! Understanding Real World Evidence (RWE) and Observational studies using Real World Data (RWD) has become necessary not only for people working in pharmacovigilance but to everyone working in all stages of the lifecycle of medicines.

Early-Bird rate for DIA Industry Members Available!

DAYS

HOURS

MINUTES

SECONDS

Faculty

Ben  Bray

Ben Bray

Health data science, Epidemiology, Real world evidence, GenAI, United Kingdom

Xabier  Garcia de Albeniz Martinez

Xabier Garcia de Albeniz Martinez

Director, Epidemiology, RTI Health Solutions, Spain

Jesper  Hallas

Jesper Hallas

Professor, Clinical Pharmacology, Pharmacy and Environmental Medicine, University of Southern Denmark, Denmark

Deborah  Layton

Deborah Layton

Director of Drug Safety, IQVIA, United Kingdom

Andrea V Margulis, DrSc, MD, FISPE

Andrea V Margulis, DrSc, MD, FISPE

Senior Director, Epidemiology, RTI Health Solutions, Spain

Dr. Margulis is a Senior Director of Epidemiology at RTI Health Solutions. She studied Medicine and completed a Pediatrics residency in Buenos Aires, completed her doctoral studies in Epidemiology at Harvard School of Public Health in Boston and did post-doctoral training at the US Food and Drug Administration. Dr. Margulis has led several multidatabase postauthorization safety studies conducted at the request of regulatory agencies. Her main research interest is pharmacoepidemiology; much of her work focuses on the safety of medical products in pregnancy. Dr. Margulis is an Associate Editor for the journal Pharmacoepidemiology and Drug Safety and serves in the Board of Directors of the International Society for Pharmacoepidemiology.

Saad  Shakir, MD, FFPM, FISPE, FRCP

Saad Shakir, MD, FFPM, FISPE, FRCP

Pharmacovigilance Physician and Pharmacoepidemiologist, ADROITVIGILANCE, United Kingdom

Saad Shakir is a pharmacoepidemiologist and drug safety physician. He has worked in the fields of pharmacovigilance, pharmacoepidemiology and risk management for 30 years, initially at the UK Regulatory Authority, then the international pharmaceutical industry and as the Director of the Drug Safety Research Unit (DSRU) in Southampton. He has led many important drug safety studies and has worked and advised on many drug safety issues including product withdrawals, major restrictions and important safety hazards. Saad will start a new stage in his career as a consultant in Pharmacovigilance and Pharmacoepidemiology on 1 June 2025

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