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Text Content

 * Investigators
 * Contact

 * About Us
   * About
   * Client Centric Approach
   * Founders
   * Senior Leadership
 * Clinical Trial Services
   * Explore All Services
   * Clinical Operations & Project Management
   * Site Feasibility & Study Start-Up
   * Medical Monitoring
   * Clinical Data Management
   * Data Monitoring Committee (DMC) Services
   * Biostatistics
   * Medical Writing
   * Clinical Trial Rescue
   * Clinical Trial Consulting
 * Resource Library
   * Explore All Resources
   * Upcoming Events
   * Explore Success Stories
   * Compare Industry Timelines
   * Download CRO Selection Checklist
 * Careers

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SETTING A HIGHER STANDARD FOR CRO PERFORMANCE

GET STUDY RESULTS FASTER

Get your results over a month faster with the industry-best biometrics timelines
PharPoint offers. See how we do it →

WORK WITH A CLIENT-CENTRIC TEAM

Our team is transparent, attentive, and accessible. Our approach →

EXPLORE OUR PROVEN SUCCESS

Learn more about how we’ve worked with companies like yours. SUCCESS STORIES →

1,000+
studies supported since 2007

Database lock
1 MONTH
faster than the industry average.

All output delivered
5 days
after database lock.


YOU’RE AN INNOVATOR FOCUSED ON IMPROVING GLOBAL HEALTH.


WE’RE HERE TO SUPPORT YOU.

 * Reduce challenges early
 * Prioritizing your data
 * Keep your custom programming

REDUCE CHALLENGES EARLY

Foreseeable factors often unnecessarily jeopardize trial success, and many of
these factors can be identified and avoided by an experienced team. One way the
PharPoint team proactively recognizes and reduces challenges is through
strategic site selection. To accomplish this, we use stringent feasibility
assessments, leverage big data and learning algorithms, lean into extensive team
experience, and evaluate cross-functional input from stakeholders across the
board.

Learn more

PRIORITIZING YOUR DATA

Our team prioritizes your data, with on-going data cleaning to get quality
results faster. Additionally, we have partnerships in place with two EDC
providers that allow us to build databases in-house and make mid-study changes
faster. In total, PharPoint’s data management team has worked in 15+ EDC
systems.

Learn more

KEEP YOUR CUSTOM PROGRAMMING

Other CROs often use proprietary macros for their programs, which leads to
problems for sponsors during the submission process.

At PharPoint, our team uses custom programming and transfers ownership to
clients at the end of a study without any added costs. This means that sponsors
who partner with us have what they need for submission.

The custom programs we create for you are yours to keep — the way it should be.
Learn more


Free Interactive Resource (UPDATED MAY 2023)


37 THINGS TO CONSIDER DURING THE CRO SELECTION PROCESS

The right contract research organization (CRO) for you is one that is a best
match for your individual study needs. While there is no one-size fits all
approach, this checklist provides a helpful guide to begin.

Download

SERVICES


PHARPOINT IS A CONTRACT RESEARCH ORGANIZATION THAT 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.

Learn more


BIOSTATISTICS & STATISTICAL PROGRAMMING

PharPoint biostatisticians all have advanced degrees and extensive experience in
the CRO industry. Since 2007, our team has supported 30+ successful regulatory
submissions.

Learn more


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 one month
faster than the industry average.

Learn more


STUDY RESCUE

PharPoint experts are an invaluable tool for studies in trouble. Members of our
leadership team average 25+ 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.

Learn more




RECENT POSTS

MEET THE PHARPOINT TEAM: SAMIA K., ASSOCIATE DIRECTOR, MEDICAL WRITING

Learn more about PharPoint’s Associate Director of Medical Writing, Samia,
including her career journey and what she think makes PharPoint unique.



Read More


HOW TO CREATE A COMPREHENSIVE CLINICAL DEVELOPMENT STRATEGY

A strategic clinical development plan (CDP) can help Sponsors optimize their new
drug programs. What should you include in your CDP?



Read More


MEET THE PHARPOINT TEAM: KENYA B., EXECUTIVE ASSISTANT

Get to know PharPoint Executive Assistant, Kenya B., as part of our Meet the
Team series.



Read More




TRUSTED BY 180+ COMPANIES LIKE YOURS.

Learn more about PharPoint’s award-winning team & services.





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Cookie Notice


Locations



5003 S Miami Blvd #100
Durham, NC 27703
Phone: (919) 433-2440

1001 Military Cutoff #301
Wilmington, NC 28405
Phone: (910) 790-0482

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 * Careers
 * Contact



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