CLINICAL TRIAL SOLUTIONS
How can we support you?
Explore our Phase II-III CRO Services
PharPoint works diligently to help clients plan, manage, and analyze effective Phase II-III clinical trials. Whether you are looking for individual service support or looking to fully outsource your trial operations, our team is happy to chat.
THE PHARPOINT DIFFERENCE
Helping sponsors meet their Phase II and Phase III study goals
AN EXPERIENCED TEAM
For Phase II-III Success
PharPoint aligns sponsors with teammates that have the right knowledge and experience to proactively identify factors critical to study success and mitigate potential study challenges. Working with the PharPoint team also means clear communication pathways and access to senior resources.
WORK COLLABORATIVELY
with a team that works without silos
From the start, the PharPoint team works collaboratively across functions to ensure study decisions are made with input from multiple perspectives. This connected approach helps us better anticipate challenges, accelerate timelines, and support deliverables that have our clients end goals in mind.
GET RESULTS FASTER
with PharPoint’s Industry-Best Biometrics Timelines
At every step, PharPoint’s standard biometrics CRO timelines are industry-best. Throughout your study, clean data are soft locked, reducing the number of subjects needing to be locked following Last Participant, Last Visit (LPLV) and decreasing the timeline to database lock to only 5 days after final Source Document Verification (SDV).
Explore Related Resources
What makes database design “smart”?
What makes database design "smart," and when should a sponsor start thinking about data collection and analysis? PharPoint programmer Michelle M. explains.
Key Components for Ensuring Quality Statistical Output
How do our experts produce quality statistical analyses? Proper planning, processes & review are critical.
How to Perform non-eCRF Data Reconciliation
How do you perform non-eCRF data (ECG, Labs, PK) reconciliation in EDC platforms like Medrio? A PharPoint clinical trial expert answers as part of our #askaclinicaltrialexpert blog series.
Choosing an EDC Provider: Ask a CRO Series
For our upcoming study, we know we want to use EDC—but there are so many options. How should we choose an EDC provider?
Adaptive Trial Design and the CRO Landscape
Learn more about the shifting CRO landscape, as PharPoint's manager of programming technologies discusses adaptive trial design and outsourcing with EDC provider Medrio.
How and When to Consider a Data Monitoring Committee
How and when should you consider a DMC (also known as a DSMB, DSMC, or IDMC)? Learn more in this brief video.
