Pharpoint Research Inc
Pharmaceutical Products Wholesaler
Why pick this one
PharPoint Research supports Phase I-IV clinical trials with in-house database builders and stated timelines of 5 days to database lock.
Best for
- Sponsors planning or conducting Phase I-IV clinical trials
- Clinical programs needing biostatistics and clinical data management
- Studies requiring CRO oversight or study rescue transitions
- Sponsors seeking stated post-database-lock biometrics timelines
- Investigators in the United States and Canada seeking clinical trial opportunities
Look elsewhere if
- Businesses seeking pharmaceutical product wholesale or retail purchasing
- Customers seeking direct medication sales or distribution
Specialties
- Phase I clinical trials
- Phase II-IV clinical trials
- Biometrics
- Biostatistics
- Clinical data management
- Clinical operations and project management
- Medical writing
- Monitoring committee support
- Quality assurance
- Site feasibility
- Study rescue transitions
What makes them different
- US-based, privately owned CRO
- Founded in 2007 by three long-time colleagues
- In-house database builders with experience across multiple EDC systems
- Provides clinical trial services for Phase I-IV studies
- Offices in Durham and Wilmington, North Carolina
- Response time
- Database lock is targeted for 5 days from last patient, last visit and final source data verification; topline results are targeted for 2 business days after database lock; draft tables, listings, and figures are targeted for 5 business days after database lock.
Distilled from this business's own website.
Contact & Location
- Address
- 1001 Military Cutoff Rd Ste 301, Wilmington, NC 28405
- Phone
- 9107900482
- Website
- http://pharpoint.com/
Services
- Clinical trial consulting
- CRO oversight
- Clinical operations
- Project management
- Biostatistics
- Data management
- Medical writing
- Quality assurance
- Site feasibility