CLINICAL TRIAL SERVICES
Medical writing for clinical trials
PharPoint’s medical writing service includes:
- Investigators’ Brochures
- Clinical Study Protocols and Protocol Amendments
- Clinical Study Reports
- Safety Update Reports
- IND and IMPD Support
EXPLORE RELATED RESOURCES
A Guide to Reviewing Regulatory Documents as a Subject Matter Expert (SME)
We discuss best practices to allow a reviewer to effectively and efficiently provide critical input to regulatory documents ...
Four Signs It is Time to Break Up with Your Regulatory Medical Writing Vendor
Explore some of the standards should you expect from your regulatory medical writing partner ...
Exploring the Characteristics of a High-Performing Medical Writing Vendor
What characteristics should you look for in your medical writing partner? We spoke with PharPoint's Associate Director of Medical Writing, ...
OUR APPROACH
Ensuring high quality medical writing deliverables
Quality and compliance come first, and our medical writing team’s quality control procedure was crafted to ensure all of our work is top-tier.
What does a great quality control procedure look like?
- Documented: We know the common pitfalls and nuances involved in different deliverables and built out a system to ensure our work is complete and quality-led, every time, without fail.
- Accountable: It’s not just checklists around here (although those are important, too). Our process is built around accountability, follow-up, and internal timelines.
- Experienced: At PharPoint, none of our deliverables are sent out without timely review and quality control checks by some of our most senior members.
