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McCormick Place

2017年6月18日 (日) 午前 8:30 - 2017年6月22日 (木) 午後 12:45

2301 South Martin Luther King Jr. Drive, Gate 4, Chicago, IL 60616

DIA 2017 Annual Meeting

Designing and Implementing a Robust Pharmacovigilance System for Vaccines

Session Chair(s)

Sanjeev  Miglani, MD

Sanjeev Miglani, MD

Founder and Director

AWINSA Life Sciences, United States

This session will provide insights into the distinct challenges in vaccine pharmacovigilance. Vaccine postmarketing surveillance is critical to mitigating risks, aiding in a response to vaccine safety concerns, and building public trust. The session will present the common need around the globe to manage public concerns about events related to vaccine safety. It will also discuss the differences in safety reporting requirements in vaccines in the US versus EU and the specific points to be taken into account in safety management and signal evaluation of vaccines both from the US and EU perspective.

Learning Objective : Discuss differences in safety reporting requirements in vaccines in the US versus EU; Recognize special considerations in safety management and signal evaluation of vaccines.

Speaker(s)

Sanjeev  Miglani, MD

Special Safety Considerations in Vaccines: US Perspective

Sanjeev Miglani, MD

AWINSA Life Sciences, United States

Founder and Director

Walter  Straus, DrMed, MD, MPH, FACP

Active Vaccine Safety Surveillance in Low- and Middle-Income Countries

Walter Straus, DrMed, MD, MPH, FACP

Moderna, United States

Vice President, Safety and PV

Seema  Jaitly, DrMed

GVP Module for Vaccine Pharmacovigilance

Seema Jaitly, DrMed

Sagittal Pharma Consulting Ltd, United Kingdom

Managing Director

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