The Industry Challenge
Clinical trial challenges are inevitable – and new advances are hard-won. While there’s arguably a certain degree of good fortune involved in research, certain obstacles shouldn’t be left to luck.
Foreseeable factors often unnecessarily jeopardize trial success, and many of these factors can be identified by an experienced team during the site selection process.
*According to Pharma Intelligence Informa
Site feasibility assessments are one of the best ways to predict enrollment speed and potential challenges. Numerous factors must be thoroughly assessed to evaluate potential sites and yield strategic and productive enrollment outcomes. PharPoint combines extensive data mining with an experienced team to help Sponsors make informed, objective decisions on which sites to select for a faster, more effective clinical trial.
INSTILL CONFIDENCE WITH DATA-DRIVEN SITE SOLUTIONS
Be confident that the sites you’re evaluating are the best ones for your study. PharPoint can perform a data-driven site search to identify viable site options on your behalf.
LEVERAGE OUR SITE RELATIONSHIPS AND EXPERTISE
Let our experts assess identified sites to determine a best-fit for your study needs – and receive a tiered recommendation for sequencing qualification, initiation, & activation.
LET US MANAGE THE ADMINISTRATIVE BURDEN
Integrate our resources into your own, and let our experts handle study startup details to support the regulatory readiness of sites.
Leverage PharPoint’s data, insights, and best practices to get into sites with access to your study’s target patient population.
Our team identifies, analyzes, and assesses sites to ensure the best possible fit for your study needs. To accurately predict enrollment rates, we leverage a proprietary Enrollment Index that projects a site’s ability to enroll patients based on patient availability, site resources, and competing trials.
PharPoint sequences qualification, initiation & activation activities to position sites for a tiered startup. This approach allows us to move fast-moving sites towards activation quickly, expediting FPI.
Identifying your ideal sites is only the first step. PharPoint has experience working with top-rated sites across the United States and leverages our relationships and best practices to keep your study top-of-mind.
PharPoint’s highly experienced clinical operations team works with sponsors, cross-functional experts, and sites to provide consultative, client-focused guidance and project management.
We’ve supported over 1,000 clinical trials and are continuing to grow and support innovators like you through high-quality services, industry-best timelines, and a transparent, client-focused approach.
PharPoint’s highly experienced clinical data management team prioritizes your data, working proactively and cross-functionally to expedite timelines after last patient, last visit.