23 October - 15:00 - 16:00 BST / 10:00 - 11:00 ET / 16:00 – 17:00 CET
From set-up to sign-off: strategies to keep submission timelines on track
For Regulatory Affairs professionals, every day matters. Missed review deadlines can mean delayed agency submissions, postponed trial starts, and lost competitive advantage. Yet many teams are still relying on SharePoint folders, email chains, and manual audit trails to manage critical submission documents.
Join our expert-led webinar to learn how companies such as Imvax, uniQure, Amarin, and a leading antibody-based biotech have cut review cycles by up to 65% — without compromising compliance.
You’ll discover how to:
• Review with internal teams, affiliates, and external partners simultaneously.
• Maintain version control and audit readiness automatically.
• Improve document quality while meeting critical deadlines.
Don’t let outdated processes put your submissions at risk. Learn how to streamline collaboration, protect timelines, and scale your review capacity for the future.
Register now to secure your place and gain the tools to transform your review process.
Speaker

Jordan Oliver, Consultant, Ideagen
Jordan supports Biotech and Biopharma organizations of all sizes to improve their speed to market by overhauling their document review processes, taking them from collaboration chaos to control. He is passionate about empowering teams to reach their regulatory filing deadlines in less time, while also improving their audit-readiness and compliance with EMA/FDA standards
This webinar is sponsored by Ideagen

Disclaimer: Whilst TOPRA is running this webinar for Ideagen, this is not an endorsement of Ideagen, Ideagen's affiliates, employees or its products and services. TOPRA is also not responsible for the content or views expressed during the webinar.
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Pricing
- Members: free
- Non-members: free
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