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Complion is committed to advancing the clinical research community through education and technology. Please enjoy our free educational resources.

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An eRegulatory Framework for the Future

Watch Complion CEO and Founder, Rick Arlow, and the VP of Product, Michele Corvino, as they review the importance...
How To Achieve a “No Findings” FDA Inspection Utilizing Remote Site Access

Read more about our client, Tekton Research, and their experience moving from paper to a “no findings” FDA inspection.
Top 5 Requirements for an Effective eReg/eISF Clinical Trial Solution

Consider these five critical areas when evaluating systems to drive efficiencies and time savings throughout your entire clinical research...
IACRN Webinar: IV Administration of Investigational Products

Webinar Objectives: You will hear from three organizations about their standard practices for IV administration of investigational products. Various issues related...
2020 Centerwatch Survey: Sponsors Place More Burden on Sites [Article]

A Complion Feature Article Varied study requirements, increasing protocol complexity, multiple amendments. Sponsors simply want to ensure the data produced by...
The Evolving Role of the Clinical Research Associate

Webinar Objectives: Discuss the professional duties of the clinical research associate. Discuss how the professional role has changed over...
Leveraging Patient Safety Science

How often have you wished for a crystal ball to help predict a serious adverse event (SAE), protocol deviation,...
Technology: Efficient Friend or Foe in Clinical Research

Webinar Objectives: Discuss the use of technology in clinical research Learn helpful technological tools to create efficiency in clinical...
Clinical Research Nursing Career Development: What’s in it for Me

Presented by: Georgie Cusack, MS, RN, AOCNS, Deirdre Hyland, RGN, RM, MSc, and Lisa Lewis, BSN, RN, CCRC Clinical Research...
Endpoints & Efficiency: How to Run Your CTO Like a PRO

Webinar Objectives: The participant will gain valuable insights into the menu of variables, and their interrelated dependencies impacting clinical...
eRegulatory: A Site's Perspective

In this webinar, Julie will discuss evaluating the site regulatory landscape, implementation of eRegulatory systems and the advantages and...
Clinical Research Nurse as Leader

Webinar Objectives: Recognize the importance of clinical research nurses (CRNs) as leaders in the clinical research enterprise. Understand the...
Achieve an Efficient Clinical Research Operation

Having an efficiently running clinical research operation is key to a successful organization. Achieving this gold standard can be...
Working With Multiple IRBs

NIH policy mandates use of a single IRB (sIRB). OHRP Common Rule regulations will expand the requirement to all...
Study Task Delegation

Does the Principal Investigator know that their responsibility for study task delegation is crucial to the proper conduct of...
Study Intensity Tool for Clinical Research

A workforce planning tool for clinical researchers adapted from US clinical research centres has helped staff in the UK...
Sign Me Up! How to Reach Your Enrollment Goals with a CTMS

We all know how hard it can be to recruit and retain patients to participate in a clinical trial....
Gateway to Compliance: Creating a Business Case for eRegulatory

This webinar addresses the business and compliance case for moving to an eRegulatory solution for clinical research documentation. If...
What ICH E6 R2 Really Means for Research Sites!

Presented by: Mary McGuire, R.N., Clinical QA Consultant at Polaris Compliance Consultants You’ve heard it before -- the revision to ICH E6...
eRegulatory Buyer's Guide

Complion’s eRegulatory Buyer’s Guide includes 38 critical considerations for selecting an eRegulatory system. This guide provides an at-a-glance perspective...