Day 3 | Wednesday, 25 October 2023 12:10 – 12:40 CET/CEST (Cent Europe Summer, GMT+2)
Spotlight Session: “Unlock the Data from your Dossiers” – Global eSubmissions track
The presentation will cover:
- Instant Regulatory impact assessment across products, dossier types and regions
- Instant document comparison across versions, products, dossier types and regions
- Instant translation of any document
- Ability to see data, documents and dossier connected
This session will be led by Celegence’s Chief Scientific Officer, Hans van Bruggen. View speaker profile here.
Register for Celegence presentation here.
GPRAS 2023: In-Person Pass
GPRAS 2023: Digital Experience Pass
GPRAS 2023 features 4 prominent topics covering everything needed to help regulatory professionals navigate, accelerate, and maintain regulatory compliance. Take a look at the full GPRAS 2023 agenda at a glance to see how you and your team can benefit!
The 4 topics across 3 days includes:
- Regulatory Information Management
- Global eSubmissions
- Regulatory Guidance and Legislative Landscape
- Regulatory Affairs in Global Markets
As a hybrid event, delegates will have the option to attend either in-person or virtually. Delegates choosing to attend virtually can attend the conference through a digital experience platform. Access all in-person sessions post-event + the digital only Global Regulatory Affairs in Global Markets track to re-cap all recordings on the days you attended.
Interested in RIM, Regulatory Guidance and Legislative Landscape and Global eSubmissions but unable to travel? Register for the digital experience pass to access all of the session recordings from the in-person Brussels Summit on-demand from 1st November.
Are you visiting the live event in Brussels? Come talk to us at Booth 17 between 23 – 25 October.
Celegence provides the pharmaceutical industry with consulting services that are tailored to the evolving operational and strategic needs of manufacturers in areas such as RIMS data management, publishing, and medical writing. We can assist you throughout the entire process to ensure that you and your business are compliant with all global pharmaceutical requirements.
Download our latest compliance services brochure for the Pharmaceutical Industry here.