CLINICAL TRIAL SERVICES

Biostatistics and Statistical Programming

Our consultative approach to our biostatistics services includes a level of responsiveness, support, and proactiveness that’s unmatched within the industry.

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.

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.

AN EXPERIENCED TEAM

PharPoint’s biostatistics team has supported over 1,000+ clinical trials since 2007. Additionally, all of our statisticians hold advanced degrees.

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

Talk with our team

PharPoint clients receive custom programming.

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

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