The Clinical Trials Guru
Portal About Me Get In The Industry Intro To Clinical Research Start A Site Consulting Podcast
PortalAbout MeGet In The IndustryIntro To Clinical ResearchStart A SiteConsultingPodcast
The Clinical Trials Guru
Clinical Trials In Plain English

When To Report an Adverse Event vs a Serious Adverse Event in Clinical Research

In this video, I answer a viewer's question on what separates an adverse event from a serious adverse event and when a Principal Investigator needs to report either in a clinical trial.

Dan SferaSeptember 12, 2016sae, ae, adverse event, side effects, safety, irb, cra, pi, study coordinators, clinical research coordinatorsComment
Facebook0 Twitter LinkedIn0 Reddit Tumblr 0 Likes
Previous

We Need To Be More Solution Oriented If We Are To Own Our Own Clinical Research Sites

Dan SferaSeptember 14, 2016entrepreneur, business, study coordinator, research site
Next

What Should Your Profit Margins Be When Running Your Own Clinical Research Center?

Dan SferaSeptember 8, 2016business, profit margins, contracts, budgets

Join Over 10,000+ Subscribers Getting Exclusive Content, Private Q&A's, Giveaways and More!

Thank you!

CRA Academy | CRC Academy | My Consulting Firm/Work With Me | Get My Book! | Archives/YouTube Channel

This site is managed by Sfera Media and DSCS Sweat Equity & Investments, LLC

All rights reserved.