Therapeutic Expertise

Our dedication to helping clients improve global health through excellent quality and customer service has provided us with deep experience across a broad range of therapeutic areas. Explore our therapeutic expertise below.

The PharPoint team has worked across multiple therapeutic areas.

We’ve successfully supported 900+ studies since 2007, including 29+ successful regulatory submissions. Our team has experience in areas including oncology, CNS (including psychiatry, pain, and neurology), dermatology, cardiovascular, infectious disease, and rare diseases, among others.

CNS

Oncology

Dermatology

Cardiology

Infectious Disease

Rare Disease

PharPoint has supported studies across 15+ therapeutic areas with industry-best biometrics timelines.

For information on PharPoint’s expertise within a specific area or indication, please contact our business development team or explore our growing library of content below.

Regardless of study indication, PharPoint is able to provide clients with industry-best biometrics timelines.

Explore Our Therapeutically Aligned Resources

For more information:

SERVICES

PharPoint has supported sponsors with studies from Phase 1 to Phase 4. Our award-winning services include:

Clinical Operations & Project Management

PharPoint’s clinical leadership team averages 20+ years of industry experience. We can provide clients support for traditional, virtual, hybrid, and remote clinical trials across a range of therapeutic areas.

Biostatistics & Statistical Programming

PharPoint’s biostatisticians all have advanced degrees and extensive experience in the CRO industry. Since 2007, our team has averaged 2 successful regulatory submissions per year.

Data Management

PharPoint’s data management team allows us to bring results to our clients faster than the average CRO. In fact, we’re able to lock a database 31 days faster than the industry average.

Study Rescue

PharPoint’s experts are an invaluable tool for studies in trouble. Members of our leadership team average 21+ years of clinical research experience. They’ve seen first hand nearly everything that can go wrong in a trial, and have innovative solutions and proactive measures to get your study back on track.