Eventarchive
Webinar: Expedite Safety Reporting Process by Integrating Clinical and Safety Solutions
Timely reporting of safety events is critical in clinical trials. However, collecting Serious Adverse Event (SAE) data from investigational sites can be costly and time consuming. Medidata Solutions...
Informa Registration of Agrochemicals in Europe 2012
With the introduction of 1107/2009 in June 2011 Registration of Agrochemicals 2012 will provide the first chance to exchange knowledge and share experiences on the implementation of...
Webinar: The EMA Guidance on XEVMPD - Challenges and Solutions to Meet the Deadline in July 2012
ASPHALION and EXTEDO would like to invite you to a joint webinar on 12 March covering the new challenges related to the EMA guidance on XEVMPD.
Kostenloses Kompaktseminar in Frankfurt: XEVMPD als erster Schritt in Richtung Regulatory Information Management System
Die von der EMA geforderte Umsetzung der EU Verordnung zum XEVMPD ist für viele Unternehmen mit sehr hohem Aufwand verbunden. Dieses Konzept bietet jedoch auch Chancen: Unternehmen erhalten damit die...
Webinar: The EMA Guidance on XEVMPD - Challenges and Solutions to Meet the Deadline in July 2012
ProductLife, epista IT & EXTEDO would like to invite you to a joint webinar on covering the new challenges related to the EMA guidance on XEVMPD. This webinar is especially for customers from the...
DIA India 5th Regulatory Conference: Evolving Global Regulatory Environment
Pharmaceutical manufacturers in India are facing many challenges within the domestic and global regulatory environment. These challenges include manufacturing and quality control, testing and...
South African Association of Pharmacists in Industry (SAAPI) Conference 2012
Meet the EXTEDO colleagues at our booth!