Document review for regulated industries - Part 2: A medical writing practitioner on when SharePoint isn't enough

Most teams know their document review process isn't working as well as it should. Missed deadlines, scope creep, version conflicts, and the constant challenge of managing external reviewers - these aren't edge cases, they're the norm. But the solution isn't always obvious when you're in the middle of it.

In this session, we sit down with Rebecca Mains, Associate Director of Medical Writing at Rapport Therapeutics, for an honest conversation about what regulated document review really looks like day-to-day. Rebecca works in phase 3 clinical programs, manages large cross-functional teams and operates under real regulatory pressure in a fast-growing company. She uses both SharePoint and Please Review and has a clear, practical view of when each belongs.

We'll cover the moments where generic collaboration tools fall short, how her team uses Please Review to control review scope and protect submission timelines and what she'd tell any medical writing or regulatory affairs team still trying to make SharePoint work for structured reviews.

If you work in pharma, life sciences or any regulated industry where documentation quality directly impacts your submission timelines - this is the session for you.