How can I access the webinar?
Simply register and you'll receive a link to watch it immediately.
Mastering external and cross-functional document reviews in medical writing and regulatory affairs
Enhance your collaboration with external and cross-functional stakeholders with this masterclass tailored for medical writing and regulatory affairs professionals.
CLOSE 
key takeaways
What you will learn
- Discover methods to streamline and secure document reviews, regardless of department or geography.
- Learn how to navigate the complexities of external collaborations while maintaining document integrity.
- Understand how to leverage technology to enhance document review efficiency and compliance.
About this event
Dive deep into document review optimization
In an era of increasingly complex regulations and stakeholder collaborations, document reviews can make or break a project. With global teams and varying time zones, ensuring the confidentiality and efficiency of document reviews is crucial. Our expert-led webinar explores streamlined strategies to overcome the common challenges of manual processes and ensure smooth, efficient reviews.
Diahann Homer
Former Director of Oncology Medical Writing, GSKDiahann Homer brings a wealth of experience from her tenure at GSK, where she led oncology medical writing efforts. She specializes in navigating the complexities of regulatory submissions and ensuring high-quality document production across global teams.
James Wilding
VP of Collaboration Solutions, IdeagenAs VP of Collaboration Solutions at Ideagen, James supports organizations across the Life Sciences industry to radically overhaul their document review processes, empowering them to reach the document completion stage in significantly less time while improving their regulatory compliance and audit readiness.
FAQ
Frequently asked questions
Can I pause and resume the webinar?
Yes, you can pause and resume the webinar at your convenience.
Do I need any special software?
Just a web browser! We’ll send you the link to access.