<img height="1" width="1" style="display:none" src="https://www.facebook.com/tr?id=213807269037206&amp;ev=PageView&amp;noscript=1">
blog-hero.jpg
Compliance In Focus
Posted by John Lehmann on Wed, Jan 17, 2018

Writing a Great Monitoring Report – From Beginning to End

Writing great monitoring reports is not just about writing the report. It requires an in depth How to Write a Great Monitoring Report Checklist.pngknowledge of the job, the study protocol, the site, their practices, the sponsor’s procedures, the monitoring plan, the report template, and of course, the regulations. Attention to visit preparation, clear notetaking during the visit, and prompt, clear report writing pays off in delivering a high-quality document. It is a difficult skill to master, but one that is rewarding, especially when faced with a regulatory inspection.

Remember, a well-written monitoring report tells the story of your clinical trial to the FDA.

Take time to download this handy checklist to help guide you through the writing process. Please share  your helpful tips on how to write a great monitoring report.

How to Write a Great Monitoring Report

Topics: Monitoring Report, Writing

imarc

Posts by Topic:

All