Medical Writing Services
PharPoint’s medical writers provide clients with:
HIGH
Quality
Quality is our number one priority, and our medical writing department is backed by a robust quality control procedure to ensure every deliverable is exactly how it should be.
An Expert
Team
Our medical writing team is overseen by our Chief Scientific Officer, and our head medical writer has over a decade of medical writing experience across multiple therapeutic areas.
TIMELY
turnaround
Our expertise allows us to deliver high-quality documents as quickly as possible. The timelines we promise, we stick to – in true PharPoint fashion.
Our Medical Writing Services Include:
- Investigators’ Brochures
- Clinical Study Protocols and Protocol Amendments
- Clinical Study Reports
- Safety Update Reports
- IND and IMPD Support
DELIVERING QUALITY, ALWAYS
At PharPoint, quality and compliance come first, and our 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.
Learn more about PharPoint’s services.
PharPoint Research is an award-winning and client-focused contract research organization (CRO) headquartered in North Carolina. PharPoint offers clients of all sizes clinical operations, medical monitoring, data management, DMC management, biostatistics, statistical programming, and medical writing services for trials from Phase 1 through Phase 4. Founded in 2007, PharPoint’s team has participated in over 1,000 clinical trials with a high business repeat rate.