Join leading consultants and industry experts in XEVMPD and IDMP. Learn about real-life experiences. Get insights into the latest progress with XEVMPD submissions and look beyond them into strategic considerations for transitioning to the ISO IDMP.
All attendees will receive a certificate of completion.
Keynote speakers:
- Andrew Marr, Marr Consultancy: A critical update on recent XEVMPD progress and developments and transition to IDMP
- Hans van Bruggen, eCTDconsultancy: XEVMPD as data standardisation exercise
- Stan van Belkum, Medicines Evaluation Board: Common European Submission Platform
- Yona Shemesh, Teva: Experiences in XEVPRM submission – Challenges in Multi Systems and Large Scale Data Integration
- Agnieszka Wróblewska, Ziaja: Getting acquainted with EDMS: Ziaja’s story
Highlights:
- Expert’s corner: immerse yourself in products demos and TEST our solutions
- Case studies: learn how industry peers tackle regulatory compliance challenges
- Round table: get answers to your questions
- Network meet your peers and top industry consultants
Cordially invited: 23-24 May 2013, Brdo, Slovenia.
Please, click here to see the full agenda and register!