2020 Centerwatch Survey: Sponsors Place More Burden on Sites [Article]

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A Complion Feature Article Varied study requirements, increasing protocol complexity, multiple amendments. Sponsors simply want to ensure the data produced by a study is sound. Research sites often feel they need to comply with what sponsors require. While sponsors may have preferred tools and technologies for handling study data, they often are open to sites using their own systems they have …

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Best Practices for Participant Safety: Assessment, Documentation and Reporting of Adverse Event (Whitepaper)

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A Complion Whitepaper Identifying and monitoring adverse events (AEs) is critical to protecting research participants and ensuring the integrity of the research trial. “Best Practices for Participant Safety: Assessment, Documentation and Reporting of Adverse Events,” draws on the considerable experience of Elizabeth Ness (MS, BSN, RN), Ilana Logvinov (RN, MSN, CCRP), and Yolanda McKinney (RN, BSN, CCRP) to help you …

Complion Case Study - South Texas Cardiovascular Consultants

Case Study: South Texas Cardiovascular Consultants, PLLC

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How Complion helped a Texas Cardiovascular Research Department reach new levels of efficiency South Texas Cardiovascular Consultants, PLLC (STCC) is a top performing, multi-site health system serving four different cardiology locations in the San Antonio area for over 20 years. Driven to uphold their reputation of providing exceptional patient care along with the highest standards in quality and accuracy, the …