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Complion

Complion is the leading software platform used by clinical research sites to manage regulatory and trial documentation. Our standardized solution helps sites reduce redundancy, eliminate duplication of documents, and provide the right people with secure access to the single source of the truth.
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Recent Posts

Mightier than the Sword, but Killing Efficiency

Posted by Complion on Mar 12, 2018 11:06:20 AM

New Webinar Examines Opportunities to Streamline Regulatory Processes with eSignatures

A pen is great for jotting down a quick reminder on a sticky note. Pens make great gifts for associates, and are inexpensive and effective swag at business conferences. You probably have a drawer full of pens in your desk, and at this very moment a pen may be staining your shirt. But that innocuous, ink-filled stick nestled in your shirt pocket can be an enormous obstacle to productivity and efficiency for your clinical research site.

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Topics: Electronic Signatures

Bio-Optronics and Complion Announce Integration to Unify Best-in-Class CTMS and eRegulatory Solutions for Clinical Research Organizations

Posted by Complion on Nov 12, 2017 11:31:02 AM

Complion_BioOptronics_Partner.pngNovember 11, 2017 – ROCHESTER, NY – Bio-Optronics, the makers of the market leader Clinical Conductor Clinical Trial Management System (CTMS), and Complion, the powerful eRegulatory and document management platform for sites, have partnered to integrate their best-in-class solutions to deliver an industry-leading solution for research organizations.

The companies are building upon their long-standing commitment to meet customer needs and develop innovative solutions to empower investigative sites to run the world’s best research. This integration introduces a highly robust application suite, enabling research organizations to operate efficiently and profitably, while maintaining compliance with 21 CFR Part 11, HIPAA, and Good Clinical Practice (GCP).

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Topics: eRegulatory, News, CTMS, Regulatory Compliance, Billing Compliance, Document Management

Q&A from "Best Practices for Participant Safety: Assessment Documentation and Reporting of Adverse Events"

Posted by Complion on Aug 18, 2017 10:10:53 AM

The following was provided by the audience question and answer session that was part of the Complion webinar, “Best Practices for Participant Safety: Assessment, Documentation & Reporting of Adverse Events,” featuring Elizabeth Ness, MS, BSN, RN at the Center for Cancer Research, NCI, Ilana Logvinov, RN, MSN, CCRP at Mayo Clinic College of Medicine, and Yolanda McKinney, RN, BSN, CCRC at the Center for Cancer Research, NCI.

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Topics: Compliance, Safety Reporting, Adverse Events

Complion to Participate in 9th Annual AACI Clinical Research Initiative Meeting

Posted by Complion on Jul 7, 2017 10:26:27 AM

Complion, the industry-leading regulatory and document management platform for clinical research sites, will be speaking and exhibiting at the 9th Annual AACI Clinical Research Initiative Meeting from July 12-13, 2017.

Complion Founder and CEO, Rick Arlow, will be conducting a vendor presentation on Thursday, July 13, entitled, Going Paperless: Managing Regulatory & Clinical Trial Documents in Complion. Mr. Arlow will discuss best practices for managing regulatory and clinical trial documentation in cancer centers. In particular, he will explore document and information management from a research enterprise perspective, defining how systems and teams can (and should) function together to centralize information and drive performance.

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Topics: News, Events

Complion to Exhibit at AAHRPP Annual Conference

Posted by Complion on May 9, 2017 9:37:21 AM

 

Complion will be exhibiting at the 2017 AAHRPP Annual Conference in Detroit Michigan from May 10th - 11th. Our team will be at booth 112 to connect with the research community and share knowledge.

Complion's 21 CFR Part 11 compliant platform helps accredited and non-accredited sites, hospitals, health systems, cancer centers and academic medical centers save time and focus on medical advancements while maintaining safety and compliance.

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Topics: News, Events

Understanding the Role of IRBs in Clinical Research: A Quick Guide

Posted by Complion on Jan 16, 2017 8:11:37 AM

The ultimate goal of clinical research is to provide relief from, if not outright cures for, the various maladies and infirmities that plague human beings. In the ever-evolving world of research, history has shown that human frailties of another variety can sometimes send the pursuit of that goal down a less noble path. Effective regulation helps to ensure that that ultimate goal remains dominant among the many motivations that drive research.

Institutional review boards are an important example of regulatory efforts to insure the protection of the rights of human research subjects, as well as the protection of the patients who will ultimately benefit from the treatments resulting from that research.

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Topics: Clinical Research Ethics, Human Subject Protection, Compliance

A History of Clinical & Human Subject Research

Posted by Complion on Jan 4, 2017 4:11:17 PM
“Discovery consists of seeing what everybody has seen and thinking what nobody has thought.”
-- Albert Szent-Gyorgy (1893-1986), winner of the 1936 Nobel Prize for Physiology and Medicine

In light of the remarkable level of technological complexity and sophistication in today’s clinical research it can be too easy to lose sight of the fact that the roots of today’s research are long and deep, spanning centuries. Each breakthrough, each moment of discovery in that long history was, as Nobel laureate Albert Szent-Gyorgy describes, a moment in which someone looked at what others had already seen and saw something new.

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Topics: Clinical Research Ethics

Streamlining Delegation of Authority Documentation in Clinical Research

Posted by Complion on Nov 8, 2016 11:39:09 AM

Effective and efficient record-keeping and documentation is the life’s blood of clinical research -- its importance can’t be overstated. A key facet of that documentation is capturing and maintaining information regarding the Investigator’s delegation of responsibilities within a clinical trial. 

The US Food and Drug Administration provides guidelines addressing the delegation of those responsibilities. But how do you transform a set of FDA guidelines into  a concrete, effective, real-world strategy for documenting that delegation?

The latest Complion feature article offers an answer to that question.

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About Complion

Complion provides clinical research sites and their sponsors with a software platform to enable secure, compliant and efficient management of documents and administrative tasks. We would love to hear from you with any questions about our Insights blog or to learn more about our software platform.

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