| 17 Avril 2013
BASEL, SWITZERLAND — 17th April, 2013 — Pharmaceutical  professionals, regulatory agencies and academics will share knowledge  and experience at DIA Europe’s conference on the Impact of the New Pharmacovigilance Legislation on Regulatory Affairs.
The event, to be held in London from 4th to 5th June, will highlight how changes in legislation will affect the way product assessment is carried out in both pre- and post-authorisation phases, introduce new obligations to Marketing Authorisation Holders, and bring in continuous benefit-risk assessment. The conference will also look at the impact of the new Pharmacovigilance Risk Assessment Committee (PRAC) on the life-cycle management of products, and the PRAC’s interactions with other committees.
Session highlights at the conference include:
To find out more, or to register, visit www.diahome.org/PhvImpact2013.
ABOUT DIA
 DIA is a neutral, global, professional, member-driven association of  nearly 18,000 professionals involved in the discovery, development, and  life cycle management of pharmaceuticals, biotechnology, medical devices  and related health care products. Through our international educational  offerings and myriad networking opportunities, DIA provides a global  forum for knowledge exchange that fosters the innovation of  products, technologies and services to improve health and well being  worldwide. Headquarters are in Horsham, Pa., USA, with offices in Basel,  Switzerland, Tokyo, Japan, Mumbai, India and Beijing, China. www.diahome.org