Insights Blog

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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