The Cancer Letter

The leading source for information on the issues that shape oncology since 1973

COVID-19 Updates

AACI’s CRI annual meeting goes virtual

Share on facebook
Share on twitter
Share on linkedin
Share on email
Share on print
BYLINE
IN THIS ISSUE
DOWNLOAD PDFTABLE OF CONTENTS

The Association of American Cancer Institutes’ Clinical Research Innovation program has moved its July 7-8 annual meeting to a virtual format.

“The health and well-being of AACI meeting attendees, exhibitors, and cancer center patients is our top priority,” AACI said in a statement. “As we plan our 2020 meetings, we are closely monitoring the coronavirus pandemic—particularly the impact of COVID-19 on travel and professional conferences.

“We believe this decision will allow us to deliver the innovative, quality education our members expect from the CRI annual meeting, while prioritizing the health and safety of attendees.”

The association said it plans to announce information on registration and virtual sessions in the coming weeks.

Table of Contents

YOU MAY BE INTERESTED IN

Regulatory News

Makary vows to speed up drug approvals and end FDA’s “cozy” relationship with industry
Commissioner promises to protect scientific integrity while bringing in “fresh” MAHA ideas

In his first sit-down interview since beginning his role as FDA commissioner 17 days earlier, Marty Makary, a former Johns Hopkins surgeon and the only Trump pick for HHS whose confirmation received Democratic support, said he would speed up approvals for rare-disease treatments by reducing reliance on animal testing and shifting towards organoids and computational models. 
By Claire Marie Porter
Guest Editorial

Regulation must keep up with scientific advances

The American Cancer Society’s recent report on the increasing incidence rates of colorectal cancer in young adults once again rang an alarm bell for adults over 45 to get checked, especially if they are having symptoms. But as an oncologist with more than 40 years of experience, I also believe that this should be a clarion call to scientists and researchers, and for regulators at the FDA.
By Richard M. Goldberg
Table of Contents

Never miss an issue!

Get alerts for our award-winning coverage in your inbox.

Login

Site license subscribers:
Log in with your IP | Register a sponsored account