Insights Blog

Streamlining Regulatory Processes with eSignatures

Q&A Follow-up from “What ICH E6(R2) Really Means for Research Sites!”

Complion to Exhibit at 2018 MAGI West

Complion Customer Receives “Exceptional” Rating from National Cancer Institute

Complion to Participate in the 2018 Global Site Solutions Summit

eRegulatory Buyer's Guide: A 38-Point Checklist for Choosing the Right Solution

University of Cincinnati Cancer Institute Abstract Awarded 1st Place for 10th Annual AACI CRI Meeting

Smart Decisions Behind a Successful FDA Inspection with eRegulatory

Clinical Site Regulatory Processes: The Case for Standards

5 Crucial Considerations for Selecting a CTMS

Leveraging eRegulatory to Improve Remote Monitoring

Mightier than the Sword, but Killing Efficiency

Rowing in the Same Direction: Integrating eRegulatory and CTMS Systems

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

Electronic Signatures in Clinical Research: Lifting the Paper Curse

Protecting Clinical Research Documents From Natural Disasters

Tough decisions? See into your eRegulatory future at 2017 Global Site Solutions Summit

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

Q&A from Document Management Success: A Guide to Part 11 System Validation

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

How a Texas Cardiovascular Research Department Reached New Levels of Efficiency

A Partner in 21 CFR Part 11 Compliance

Taming the Email Beast with eRegulatory

Complion to Speak at 2017 MAGI East Conference

Multi-Site Trials: Streamlining Operations with eRegulatory & Document Management

Complion to Exhibit at AAHRPP Annual Conference

The Future of Clinical Research: Single-Drug Studies

Meet Complion at ACRP’s Annual Meeting & Expo

Complion Founder Rick Arlow to Co-Host SCRS Webinar

Complion Article Featured in ACRP’s Flagship Journal, Clinical Researcher

The Paperless Voyage: How Leading Sites Can Overcome Fear of Sponsor Resistance when Adopting an eRegulatory System

The Future of Clinical Research: Site Selection

Steps to Paperless Research Sites: Creating Certified Copies & More

The Future of Clinical Research Technology

The Future of Clinical Research: Introduction

The Paperless Research Site: Best Practices for eRegulatory and Document Management

The Basics of Coverage Analysis

Complion CEO to Speak at 11th Clinical Trial Billing & Research Compliance Conference

Why are Sites Slow to Adopt Paperless Technologies?

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

A History of Clinical & Human Subject Research

Streamlining Delegation of Authority Documentation in Clinical Research

Recruitment & Retention in Pediatric Clinical Research Trials

Going Paperless: A Shared Journey

Complion to Exhibit at MAGI's Clinical Research Conference - 2016 West

Complion to Exhibit at 2016 Global Site Solutions Summit

Complion to Exhibit at SOCRA 25th Annual Conference

FDA Inspections Need Not Be Stressful: A Q&A With Dr. Harvey Arbit

A Learning Experience: eRegulatory from a Site Without Binders

Q&A from eRegulatory Experiences from a Site Without Binders

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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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