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Jun 04 2025 - Jun 04 2025
12:00 BST
Fast-tracking regulatory submissions in Biotech: How to cut review time by 65%
Is document review the hidden threat to your submission timeline?
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Key takeaways:
Follow in UniQure, Amarin and Imvax's footsteps.
Don't just take our word for it -- see the results we've had from working with Imvax, uniQure and Amarin, as well as an international Biotech specialising in antibody-based therapeutics.
- Streamline document review cycles by 65% - Review simultaneously with teams of all sizes (including external reviewers), regardless of document length or complexity.
- Get to market faster than the competition - Every week gained in clinical trial readiness or submission equals a commercial edge.
- Meet critical regulatory deadlines with confidence - Avoid costly submission delays with version control, audit trails, and real-time collaboration.
- Maximise review performance with a leaner team - Do more with less: scale document reviews without scaling headcount.
- Deliver higher quality documents, faster - Reduce errors, missed comments, and rework with structured, collaborative review workflows.
- Scale for the future - Leave slow, manual collaboration behind you. Set yourself up for success as you grow.
About this webinar:
Is document review the hidden threat to your submission timeline?
In our upcoming webinar, we'll be sharing how to resolve the 'SharePoint headaches' that slow down Biotech submission timelines. If version confusion, comment chaos, manual audit trails and corrupted documents sound familiar, you're not alone. Yet many Biotech and Biopharma companies are still using inefficient document review methods that add weeks -- or even months -- to their timelines.
Maybe you're 'coping' with SharePoint and email chains for now. But as your business grows, you simply can't afford to have slow and manual collaboration processes slowing down your speed to market. Join us for a live, expert-led webinar where be sharing real-life examples of Biotech companies similar to yours that have streamlined document collaboration and cut review cycles by up to 65%.
Meet our speaker
Jordan Oliver
Solutions Consultant, IdeagenJordan 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.
FAQ
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Absolutely! You can submit questions during the broadcast.