With the release of version 2.0, em-PACT now features an updated study activity hierarchy, increased automation of tasks, more detailed and flexible work queues, plus new metrics and reports to identify additional opportunities for improvement. Contact us to learn more about how em-PACT can help reduce your study activation timelines.
About em-PACT
Opening new clinical trials to patients quickly, efficiently and safely is a critical measure of any research organization’s performance. Each extra day it takes to open a study results in lost opportunities for patients, additional costs to the organization, and potentially diminished scientific relevance of the trial.
Is decreasing study activation timelines a priority at your site?
- Do you currently have an easily accessible and holistic view of your full activation pipeline?
- Are you using a defined methodology to manage the complexities of continuously launching multiple studies?
- Does your management team have real-time access to critical metrics about timelines, workload, and quality to understand how well their teams are performing?
em-PACT is a cloud-based eManaged Protocol Activation approach that will improve processes and reduce timelines in all aspects of the trial activation process by:
If reducing study activation timelines is a priority at your site, contact us to learn how em-PACT can help you achieve your activation goals.
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