Resource Library
Complion is committed to advancing the clinical research community through education and technology. Please enjoy our free educational resources.
Featured Resources
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Article | compliance | Featured Content | regulatoryA 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 of... -
Article | Featured ContentComplion’s eRegulatory Buyer’s Guide includes 38 critical considerations for selecting an eRegulatory system. This guide provides an at-a-glance perspective on functionality, visibility, scalability, ... -
Article | Featured ContentICH E6 guidelines have been revised to reflect two decades of technological changes. Among these changes, include updated standards regarding electronic records and essential documents. Learn how Com... -
Article | Featured ContentThe Complion Regulatory Cost Analysis helps investigative sites quantify the burden of regulatory compliance and identify opportunities for improvement.
All Resources
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IACRN | On-Demand Webinar | webinarWebinar Objectives: You will hear from three organizations about their standard practices for IV administration of investigational products. Various issues related to IV product administration w... -
Article | compliance | Featured Content | regulatoryA 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 of...
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On-Demand Webinar | Ramon Adams | webinarWebinar Objectives: Discuss the professional duties of the clinical research associate. Discuss how the professional role has changed over time. Discuss how the clinical research asso... -
IACRN | Laura Lee | On-Demand Webinar | webinarHow often have you wished for a crystal ball to help predict a serious adverse event (SAE), protocol deviation, or clinical care error associated with clinical research? If only we had the ability to ... -
Janelle Allen | On-Demand WebinarWebinar Objectives: Discuss the use of technology in clinical research Learn helpful technological tools to create efficiency in clinical research Review best practices for electronic produ... -
Deirdre Hyland | Georgie Cusack | IACRN | Lisa Lewis | On-Demand WebinarPresented by: Georgie Cusack, MS, RN, AOCNS, Deirdre Hyland, RGN, RM, MSc, and Lisa Lewis, BSN, RN, CCRC Clinical Research Nurses (CRNs) work in a variety of roles within the clinical research ent... -
Jean Gatewood | On-Demand Webinar | webinarWebinar Objectives: The participant will gain valuable insights into the menu of variables, and their interrelated dependencies impacting clinical research efficiencies The program will delive... -
Julia Brenner | On-Demand WebinarIn this webinar, Julie will discuss evaluating the site regulatory landscape, implementation of eRegulatory systems and the advantages and challenges. Webinar Objectives: Understand the start-... -
IACRN | On-Demand Webinar | Sharon Flynn | Tamara Kempken MehringWebinar Objectives: Recognize the importance of clinical research nurses (CRNs) as leaders in the clinical research enterprise. Understand the importance of clinical research nurse (CRN) leade... -
Andy Tolman | Jill K. Shilbauer | On-Demand WebinarHaving an efficiently running clinical research operation is key to a successful organization. Achieving this gold standard can be difficult, but it is certainly attainable. What does your study pipe... -
James Riddle | On-Demand Webinar | webinarNIH policy mandates use of a single IRB (sIRB). OHRP Common Rule regulations will expand the requirement to all federal research in January 2020, and the FDA may issue similar requirements as part of... -
On-Demand Webinar | Velma Marzinotto | webinarDoes the Principal Investigator know that their responsibility for study task delegation is crucial to the proper conduct of a clinical trial? Is the PI aware of the revisions in ICH GCP E6(R2) regard... -
Joanna Gray | On-Demand WebinarA workforce planning tool for clinical researchers adapted from US clinical research centres has helped staff in the UK with widely accepted metrics that provide recognised, valuable data and evidence... -
Crystal Mendenhall | On-Demand WebinarWe all know how hard it can be to recruit and retain patients to participate in a clinical trial. Technology can be a life saver, but many companies don’t know the best way to implement technology int... -
Leslie Korbee | On-Demand WebinarThis webinar addresses the business and compliance case for moving to an eRegulatory solution for clinical research documentation. If you are uncertain if your institution or your team can... -
Mary McGuire | On-Demand WebinarPresented by: Mary McGuire, R.N., Clinical QA Consultant at Polaris Compliance Consultants You’ve heard it before -- the revision to ICH E6 includes many new elements; an emphasis on,... -
Article | Featured ContentComplion’s eRegulatory Buyer’s Guide includes 38 critical considerations for selecting an eRegulatory system. This guide provides an at-a-glance perspective on functionality, visibility, scalability, ...
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Article | Featured ContentICH E6 guidelines have been revised to reflect two decades of technological changes. Among these changes, include updated standards regarding electronic records and essential documents. Learn how Com...
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ArticleA 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 Partic... -
ArticleHow 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 servi...
