Meet Ideagen at AMWA 2025, table #3 and discover faster, more collaborative and fully compliant ways to manage complex medical writing reviews.
Plus, get a wireless bamboo phone charger just for booking!
Meet with our team at AMWA 2025, at table #3, to explore how leading life sciences organizations are transforming their regulatory and medical writing review processes. We’ll share practical strategies to:
Faster document review cycles on average
Average cost savings compared to manual review processes
Of the top 25 pharma companies trust Ideagen
Page regulatory dossiers handled with ease
With Ideagen Please Review, you are able to see all activity occurring from all participants in your document reviews in real time.
Watch our intro video to collaboration and redaction to find out more.
Trusted, compliant and fast.
Collaborate in real time with unlimited reviewers and accelerate regulatory submissions from weeks to days.
Maintain CFR Part 11, GLP and HIPAA compliance with full audit trails, electronic signatures and validated systems.
See every comment, track every change, and keep reviews organized with role-based permissions and automated reports.
Used daily for CSRs, BLAs, INDs and SOPs by leading biotech, pharma and medical device organizations.
Pre-book a meeting and get a complimentary bamboo phone charger when you meet us onsite. It’s our thanks for connecting early to explore smarter, faster document reviews.