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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Featured Content | IACRN | Upcoming Webinar | webinarBy the end of this session, the learner will be able to: Define re-consent and reaffirmation. Explain three types of research situations that warrant participant re-consenting. Discuss the ... -
Article | Featured ContentA Complion Feature Article There are many research documents, forms, and agreements that require signature. But when time is spent compiling paperwork and chasing down signatures, Physicians an... -
Article | Featured ContentDownload your 38-Point Checklist for Choosing an eRegulatory Solution Complion’s new eRegulatory Buyer’s Guide includes 38 critical considerations for selecting an eRegulatory system. This guide prov... -
Article | Featured ContentA new case study from Complion shares insights into Chesapeake Research Group's (CRG) FDA inspection while using the Complion eRegulatory system. -
Article | Featured ContentHow Complion helps clinical research sites meet new changes Facilitating Compliance with ICH-GCP E6 R2 - 450pxWhen the original ICH E6(R1) was released in 1996, clinical trials were performed in a ... -
Article | Featured ContentHow 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... -
Featured Content | On-Demand WebinarComplion Founder and CEO Rick Arlow, will discuss how an eRegulatory and document system can complement and connect with CTMS and other systems to save time, improve compliance and access. Explore bes... -
Article | Featured ContentBased on a survey and findings from CenterWatch, the Complion Regulatory Cost Analysis helps investigative sites quantify the burden of regulatory compliance and identify opportunities for improvement... -
Article | Featured ContentWhile your organization may be working in the shadow of a growing mountain of paper documents and regulatory binders, the prospect of transitioning to an electronic document management system can be d... -
Article | Featured ContentThis article examines the use of electronic tools for maintaining regulatory compliance at research sites, and recommends best practices to be applied to the use of those tools. The information presen...
All Resources
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Featured Content | IACRN | Upcoming Webinar | webinarBy the end of this session, the learner will be able to: Define re-consent and reaffirmation. Explain three types of research situations that warrant participant re-consenting. Discuss the ...
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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 Elucidate best practices for electronic pr... -
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... -
Article | Featured ContentA Complion Feature Article There are many research documents, forms, and agreements that require signature. But when time is spent compiling paperwork and chasing down signatures, Physicians an...
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Article | Featured ContentDownload your 38-Point Checklist for Choosing an eRegulatory Solution Complion’s new eRegulatory Buyer’s Guide includes 38 critical considerations for selecting an eRegulatory system. This guide prov...
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Article | Featured ContentA new case study from Complion shares insights into Chesapeake Research Group's (CRG) FDA inspection while using the Complion eRegulatory system.
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Article | Featured ContentHow Complion helps clinical research sites meet new changes Facilitating Compliance with ICH-GCP E6 R2 - 450pxWhen the original ICH E6(R1) was released in 1996, clinical trials were performed in a ...
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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... -
Article | Featured ContentHow 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...
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ArticleAs more sites are looking to implement technology to go paperless, improve standardization, and provide secure access to essential documents, site staff ’s experience with ensuring compliance with 21 ...