EUDRAC will be exhibiting at the DIA Annual Meeting in San Diego, California, from 23 rd to 27 th of June 2019. We have developed and executed regulatory strategy for numerous clients, operating both in the EU and the US markets. If you are interested in discussing your potential Regulatory Affairs...
Read moreDIA 2019 Vienna EUDRAC will be exhibiting at the annual DIA Europe Meeting in Vienna, Austria from 5th - 7th February 2019. Our team would be pleased to welcome you at booth number B70 to discuss your potential regulatory affairs, pharmacovigilance and publishing needs. A member of our Management...
Read moreCarole Pugh and Karen Goode of EUDRAC attended the recent reception hosted by Prince Charles at Buckingham Palace to celebrate the winners of the 2018 Queen’s Awards for Enterprise. The reception was held in the impressive state rooms at Buckingham Palace with the Duke of Kent also in attendance...
Read moreEUDRAC will be exhibiting at the annual DIA Annual Meeting in Boston, United States of America from 24th to 28th June 2018. Our team would be pleased to welcome you at booth number 1143 to discuss your potential regulatory affairs, pharmacovigilance and publishing needs. A member of our Management...
Read moreEUDRAC will be exhibiting at the annual DIA Annual Meeting in Basel, Switzerland from 17th – 19th April 2018. Our team would be pleased to welcome you at booth number 41 to discuss your potential regulatory affairs, pharmacovigilance and publishing needs. A member of our Management Team will be...
Read moreWhere: Evenlode Boardroom, Milton Park Innovation Centre When: 22 November 2017 at 10:00 Topics: Early-to-late phase clinical trial pharmacovigilance Preparation for Marketing Authorisation Pharmacovigilance auditing and training Common pharmacovigilance inspection findings and pitfalls (MHRA,...
Read moreEUDRAC will be exhibiting at the annual DIA Annual Meeting in Chicago, IL, USA from 18th – 22nd June 2017. Our team would be pleased to welcome you at booth number 757 to discuss your potential regulatory affairs, pharmacovigilance and publishing needs. A member of our Management Team will be there...
Read more