A full-service, highly qualified partner who uses effective technology-enabled financial management services can help ensure efficient site payments, greater transparency into payments on all sides, and satisfied investigators.
Understand the benefits and challenges of conducting studies in Latin America in addition to some recent changes that could expedite regulatory timelines.
How global site networks can effectively address timeline, budget and data quality concerns, by providing access to multiple experienced sites within a single network, providing cost savings through reduction of the total number of sites used and recruitment of a large volume of patients.
Four ways to successfully guide and reshape clinical trials to meet the needs of our ever changing social, economic and regulatory climate.
How to get the most of out of your UAT process and focus your efforts where they should be.
Six things that high-performing clinical research sites do that make sponsors return to them again and again.
Increasingly central in the course of drug development is the inclusion of observational studies, including registries, which provide insights missing from traditional interventional studies.
This white paper discusses the role of the pharmacy in a modern day Phase I clinical research unit and its role in understanding the safety and pharmacology of a drug before Phase II can begin.
How the right team and tools can make all the difference in clinical trial rescue scenarios.
Take advantage of advanced security and compliance services to ensure that users are safe operating in a cloud environment and benefit from the scalability and business continuity of cloud computing.
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