PharPoint Research, Inc.
PharPoint Research is a US-based, privately owned contract research organization (CRO) founded in 2007. It provides flexible, specialized clinical development services from pre-IND to Phase 4, supporting over 1,000 clinical trials across various therapeutic areas. The company emphasizes a client-centric, transparent, and collaborative approach, aiming to deliver high-quality, faster study results while fostering a supportive and innovative work environment.
Industries
Nr. of Employees
medium (51-250)
PharPoint Research, Inc.
Products
Full-Service
Comprehensive Phase I CRO services leveraging robust early phase experience, industry-best biometrics timelines, and strong site partnerships to help clients pursue clinical study success.
Full-Service Clinical Trial CRO Services
PharPoint offers client-centric, consultative, and transparent clinical development and trial CRO services without silos.
Biometrics
Clinical biostatistics and data management services including database build, mid-study changes, database lock, top-line results, and clinical study report (CSR) delivery.
Phase II-IV
Comprehensive clinical trial support and full-service CRO solutions for Phase II and III clinical trials, including planning, management, and analysis.
Phase II-III CRO Services
Comprehensive clinical trial support and full-service CRO solutions for Phase II and III clinical trials, including planning, management, and analysis.
Clinical Trial
Full-scale study remediation, consultative support, and oversight services designed to regain clinical trial transparency, boost data cleanliness, and get troubled studies back on track.
Full-Service
Comprehensive Phase I CRO services leveraging robust early phase experience, industry-best biometrics timelines, and strong site partnerships to help clients pursue clinical study success.
Full-Service Clinical Trial CRO Services
PharPoint offers client-centric, consultative, and transparent clinical development and trial CRO services without silos.
Biometrics
Clinical biostatistics and data management services including database build, mid-study changes, database lock, top-line results, and clinical study report (CSR) delivery.
Phase II-IV
Comprehensive clinical trial support and full-service CRO solutions for Phase II and III clinical trials, including planning, management, and analysis.
Phase II-III CRO Services
Comprehensive clinical trial support and full-service CRO solutions for Phase II and III clinical trials, including planning, management, and analysis.
Clinical Trial
Full-scale study remediation, consultative support, and oversight services designed to regain clinical trial transparency, boost data cleanliness, and get troubled studies back on track.
Services
Regulatory, clinical, medical, and biometrics consulting to support development planning, pre-IND interactions, and study strategy.
Objective site evaluation, activation processes, and contract negotiation support to accelerate study initiation and first patient in.
Database strategy and build, eCRF design, data cleaning, reconciliation, query management, and support for rapid database lock.
Sample size and simulation support, SAP development, randomization schedules, dataset creation (SDTM/ADaM), and TLF programming for analysis and regulatory submissions.
Site and operations oversight by CRAs, COLs, and PMs to manage conduct, compliance, monitoring, and issue escalation during study execution.
Integrated study physician support to advise on medical issues, safety assessments, and clinical decisions.
Regulatory, clinical, medical, and biometrics consulting to support development planning, pre-IND interactions, and study strategy.
Objective site evaluation, activation processes, and contract negotiation support to accelerate study initiation and first patient in.
Database strategy and build, eCRF design, data cleaning, reconciliation, query management, and support for rapid database lock.
Sample size and simulation support, SAP development, randomization schedules, dataset creation (SDTM/ADaM), and TLF programming for analysis and regulatory submissions.
Site and operations oversight by CRAs, COLs, and PMs to manage conduct, compliance, monitoring, and issue escalation during study execution.
Integrated study physician support to advise on medical issues, safety assessments, and clinical decisions.
Expertise Areas
- Clinical trial management
- Site feasibility and start-up
- Clinical data management
- Biostatistics and statistical programming
Key Technologies
- Electronic data capture (EDC) systems
- ePRO and eClinRO
- Telemedicine and virtual visit platforms
- Wearables and peripheral device integration
News & Updates
A success story of a dermatology study that exceeded enrollment expectations and finished early.
A case study of an oncology trial that achieved early completion of the last patient visit.
A case of intervention to improve a neonatal study that was underperforming with a previous CRO.
A guide on how PharPoint supports faster clinical trial timelines through efficient biometrics processes.
PharPoint was named a Best Place to Work in 2023 and 2024 by the Triangle Business Journal.
Received the 'Most Innovative CRO' award from the Triangle Business Journal in 2020.
A success story of a dermatology study that exceeded enrollment expectations and finished early.
A case study of an oncology trial that achieved early completion of the last patient visit.
A case of intervention to improve a neonatal study that was underperforming with a previous CRO.
A guide on how PharPoint supports faster clinical trial timelines through efficient biometrics processes.
PharPoint was named a Best Place to Work in 2023 and 2024 by the Triangle Business Journal.
Received the 'Most Innovative CRO' award from the Triangle Business Journal in 2020.