Powerful collaboration
Look to PharmaLink to manage every aspect of your clinical trial with unrivaled proficiency, from protocol development through final reporting. Speed and ease are inherent to our eClinical process—important considerations as trial costs soar and the pressure to bring new drugs to market intensifies. But eClinical is not just about collecting data faster. It's also about managing information better and sharing critical information among the entire study team for more confident decision making, building a powerful environment of continuous shared knowledge.

Transparency and accountability
As site researchers simultaneously record and query data online, our program managers, data managers, medical monitors and CRAs continuously review and query those data. Is the information valid? Does it make clinical sense? What-ifs are considered when providing informative trial status reports throughout your study—a blend of clinical data and comprehensive management information. Accountable in real time, we're aware that our performance can be monitored at any time. The result is unusually high level of responsiveness and integrity that builds trust and collaboration.

Insight into your trial
While PharmaLink incorporates the most widely used EDC software available, clinical teams must have access to more than CRF data to successfully manage a trial. For this reason we exclusively developed InfoLink, an advanced web-based clinical trial management system. InfoLink "sits on top" of the clinical database, pulling requested data into manageable reports to utilize on a day-to-day, if not hourly basis, including such vital information as monitoring visit schedules, regulatory document status, and patient enrollment progress to plan, to name a few. With InfoLink, you get real time data reporting, continually refreshing as data are entered - not just the posting of latent reports found in most CTMS systems.  

More confident decision making
InfoLink aggregates and disseminates both clinical and study progress data into an easy-to-read format—for progressive, real-time study management. It's how we've solved your quandary of making costly decisions based on incomplete or outdated information. Early access to accurate, useful information lets you make adjustments proactively as the trial moves forward. It's a dynamic approach that's not possible with paper or EDC alone.

Greater control
With PharmaLink there are no surprises or setbacks at a trial's completion. Whether identifying safety trends, learning that a drug in a Phase I trial is not performing, or rectifying recruitment problems, you monitor and act on events as they happen. And because you measure our performance on an ongoing basis, you experience greater control and input from your outsourcing partner than ever before.

Smarter trials
With PharmaLink as your partner, you'll witness a better way to implement and manage your clinical trials. Our blending of clinical expertise, leading edge technology and process enhancements allow us to deliver a more efficient, smarter clinical trial. Leverage our expertise to:

• Proactively identify and resolve critical issues before its too late
• Make "go/no go" decisions earlier on based on cleaner/faster data
• Gain knowledge of the trial's status 24/7
• Ensure sites have a positive experience utilizing EDC
• Enjoy uneventful database locks in days instead of months