CLINICAL TRIAL SERVICES
Biostatistics CRO services
With PharPoint’s biostatisticians and statistical programmers, clients receive access to our:
EXPERIENCED TEAM
PharPoint’s biostatistics team has been trusted by clients since 2007. All of PharPoint biostatisticians hold advanced degrees.
INDUSTRY-BEST TIMELINES
PharPoint’s biostatistics team works diligently to expedite the delivery of study results. Our standard timelines include the delivery of top line results two days after database lock, and the delivery of draft TLFs three days following.
REGULATORY EXPERIENCE
PharPoint’s biostatistics team has supported over 30 regulatory submissions and has experience supporting discussion with regulatory authorities, including type A, B, and C meetings.
PharPoint’s biostatistics CRO services include:
- Randomization
- Regulatory and advisory meeting support
- Statistical analysis plans (SAP)
- Statistical analysis and support services for interim, futility, and Data Monitoring Committee (DMC) analysis
- Integrated summaries of safety and efficacy
- Preparation of case report tabulations (CRTs)
- Quantitative epidemiology including patient registries
EXPLORE RELATED RESOURCES
PharPoint Incorporates EDC Software Medrio into Data Management Offerings
Explore how PharPoint Research integrates Medrio's EDC software into its data management offerings to enhance clinical trial efficiency. Discover the benefits of streamlined data collection, improved accuracy, and accelerated study timelines with Medrio's innovative solutions.
PharPoint joins Medidata Solutions’ CRO partner program
Medidata Solutions announced that PharPoint has joined Medidata’s ASPire to Win® channel partner program.
OUR UNIQUE APPROACH
All PharPoint clients receive custom programming. Why?
Personalization
Clients receive programs catered to their study needs and preferences
Pricing transparency
No hidden fees due to use of proprietary compiled macros
Transferability
Clients have the ability to use PharPoint programming to create datasets and TLFs in-house
Submission readiness
Programs can easily be packaged as part of regulatory submission