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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Kelly Willenberg | Upcoming 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 ... -
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 ... -
Featured Content | 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 paperwork ... -
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... -
Article | Featured ContentAs 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 ... -
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 ContentInsight and expertise from Betsy Fallen, a regulatory and clinical process consultant, on using information technology to tame the paper beast that threatens efficiency and productivity at clinical re... -
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...
All Resources
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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... -
Featured Content | 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 paperwork ...
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On-Demand WebinarPresented by: Velma Marzinotto, BScN, RN, CCRP In the demanding world of clinical research, it is imperative that Investigators know and follow the rules in order to conduct a research study succes... -
Norman M. Goldfarb | On-Demand WebinarIn this eye-opening webinar, Norman M. Goldfarb, MAGI Chairman and Editor of the Journal of Clinical Research Best Practices, will explain what FMV really means. Study sponsors and CROs have good reas... -
On-Demand Webinar | Tamara Kempken MehringPresented by: Mary Jane Williams, DNP, MPH, RN, NE-BC and Tamara Kempken Mehring, MSN, RN, CCRC CRNs will recognize how Standards 7, 9, 10, 11 of Professional Performance and their associated compe... -
Kunal Sampat | On-Demand WebinarPresented by: Kunal Sampat: Proven strategies that can help you get your study budget approved in less than 2 weeks. -
Kelly Willenberg | On-Demand WebinarPresented by: Kelly Willenberg, DBA, RN, CCRP, CHRC, CHC | This webinar will discuss these important areas and how to make your holidays brighter in billing compliance! -
On-Demand Webinar | Velma MarzinottoThis webinar will outline all the steps required to launch a trial from the study site’s perspective. We will also discuss a practical and systematic approach to obtaining essential study documentatio... -
David B Russell | On-Demand WebinarAs research funds are becoming increasingly competitive, a frequent question asked is, “How much should we pay investigators for their work on a clinical trial and what methodology should be used?”.... -
On-Demand Webinar | Tamara Kempken MehringDuring this webinar, we will discuss the overarching concepts of patient and family centered care and how we as clinical research nurses can integrate the concept into clinical research. We will also ... -
On-Demand WebinarLeveraging the cloud is fast becoming a mainstream discussion within Pharmaceutical and Life Sciences companies – most employing a ‘cloud first strategy’ to deploying new applications and systems. Des... -
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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On-Demand WebinarIn order for a research enterprise to be financially viable, it is critical that the structure for resource consumption be optimized to the highest levels of efficiency. While research program structu... -
Article | How-To VideoGuidance on System Validation for Clinical Research Sites According to FDA 21CFR Part 11 and ICH-GCP E6 (R2), clinical research sites that rely on electronic records or electronic signatures ... -
How-To Video | On-Demand Webinar | ValidationDoes your site keep electronic documents using internal tools (e.g. shared drives, USBs, CDs), a third-party eRegulatory and document system, or in another solution (e.g. Box, Dropbox, SharePoint)? ...