Resources 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 | James Riddle | Upcoming 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... -
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 | James Riddle | Upcoming 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...
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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... -
Janelle Allen | On-Demand Webinar | webinarJanelle Allen will discuss the wonderful world of clinical research careers during our Wednesday, May 22nd Complion Webinar. She will delve into the current status of clinical research positions withi... -
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... -
On-Demand Webinar | Rhonda PazVital Signs of Research Performance Educational Webinar Presented by: Rhonda Paz, PhD, CRCP, Chief Executive Officer of Phase Up Running a successful research program requires integration of many ... -
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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KC Clevenger | On-Demand Webinar | Sharon Flynn | Tamara Kempken MehringEducational Webinar Since 2005 the use of oral agents in clinical trials has increased and exponential growth is expected. In clinical trials with oral agents, participants may not be adhering to s... -
Janelle Allen | On-Demand WebinarPresented by: Janelle Allen, BS, MS, CCRP, Director of Clinical Research Operations, Quality, & Education Learn practical ways to help organize your day-to-day clinical research tasks will be d... -
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 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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Elizabeth Couch | On-Demand Webinar | Rhonda HoffmanCentralized Clinical Trials Office (CTO): Best Practices & Challenges Presented by: Rhonda Hoffman, System Director of Research and Elizabeth Couch, BA, CCRP, Manager of Research Regulatory Ope... -
Kelly Willenberg | On-Demand WebinarPresented by: Kelly Willenberg, DBA, RN, CCRP, CHRC, CHC Learn the ways to make employees happy in their jobs! Webinar objectives: Demonstrate a positive attitude and give praise when it is ... -
Mary Pat Cottengim | On-Demand WebinarJoin Mary Pat Cottengim, User Experience Manager at Bio-Optronics as she will discuss new technology and how it can be utilized at your organization. -
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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Anna Canty | On-Demand WebinarHow do you know the insurance coverage offered for a trial is appropriate to the level of risk? Are you leaving gaps in coverage with the contract language you are agreeing to? How do you read an in... -
Grace-Ann Fasaye | Kathleen Calzone | On-Demand WebinarGenetic/genomic science and technologies influence the entire healthcare continuum and therefore are fundamental to all healthcare professions in both the research and practice settings. This presenta... -
Jeremy Rigby | Neal Surasky | On-Demand WebinarPresented by: Jeremy Rigby, MBA, Neal Surasky, CCRC & Lisa Bozza Archer There are many research documents, forms, and agreements that require signature. But when time is spent compiling paperwo...