EXTEDO's Software and Service Solutions for Electronic Regulatory Affairs
- Product Registration Planning & Tracking (XEVMPD, IDMP)
- Submission Management (eCTD, CTD, NeeS, CADDY, ePRISM, eIndex, eNTA , vNeeS)
- Pharmacovigilance Management (SUSAR, ICSR, PSUR, E2B)
- Labeling Management and
- Document Management
News
Summary of important topics announced at the EMA Information Day on IDMP on May 8th in London
This information was gathered at the EMA Information day by EXTEDO's expert Christian Kravogel.
EXTEDO Adds Submission Consulting Group to Network of Global Partners
Berwyn, PA – May 8, 2012 – EXTEDO, a key eRegulatory Affairs solutions provider for life sciences firms, today announced the addition of Submission Consulting Group, a life sciences consulting firm...
EXTEDO Announces the Availability of a New Solution to Help Life Sciences Firms Comply with New European Drug Safety Regulations
EXTEDO MPDmanager Supports New XEVMPD Submission Standard
Events
32th / XXXII Symposium de AEFI: “Cambio de estrategias para un sector en transformación"
Visit EXTEDO in the exhibition area!
DIA 48th Annual Meeting 2012
DIA 2012 is the largest multidisciplinary event that brings together a global network of professionals to foster innovation that will lead to the development of safe and effective health care...
eCTD für Anwender (Forum Institut)
Computer-Workshop und Fachvorträge - inkl. der neuen Validierungskriterien


