When you’re working with a big name, “big-box” CRO, there are a few pitfalls to watch out for as a small to mid-sized biotech or pharmaceutical company.
Explore PharPoint’s values in action: what makes the team at PharPoint different?
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.
For our upcoming study, we know we want to use EDC—but there are so many options. How should we choose an EDC provider? As part of our Ask a Clinical Trial Expert blog series, a PharPoint clinical trial expert answers.
We’re worried that the service providers working on our study are causing it to fall behind. Timelines are being missed due to slow enrollment and data quality is poor. What are our options? A member of the PharPoint leadership team discusses options for study rescues in this Ask a Clinical Trial Expert blog series post.
For years, pharmaceutical and biotechnology companies have employed the strategy of establishing preferred provider relationships in order to streamline the process of outsourcing clinical research studies. Often, the preferred provider would provide discounts to their customers based on efficiencies the service provider may realize from working on multiple trials for a single compound or the…
Patient recruitment used to be an ad hoc affair, where sites were personally selected by a sponsor and given a few hundred dollars to create local awareness for a clinical trial. The sponsor’s hope was that the investigator grants would be competitive enough to keep sites motivated, but unsurprisingly this approach resulted in numerous trials…
At PharPoint, we pride ourselves on producing quality statistical analyses. How are we so confident in the quality of our product? Find out in this video with Senior Manager of Statistical Programming Tracy Pflaumer and Manager of Statistical Programming Amber Urban.
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