“In March 2011 FDA finalized guidance on exception of informed consent requirements for emergency research…” To see our COO’s full guest blog entry, click here.
Please join us for an informative Webinar: 3pm EST on June 9, 2011 “Integrating and Sustaining Clinical Research” features Pearl IRB COO, Gretchen Miller Bowker Offering 1.5 hours of CE credit REGISTER NOW ABOUT THE WEBINAR Does your organization or...
It’s all about risk definition for device recalls A recent article in The Archives of Internal Medicine entitled Medical Device Recalls and the FDA Approval Process, reviews and challenges the apparent lack of device class designation linkage to recall risk. ...
Recently our co-founders, Diana Caldwell and Gretchen Bowker were interviewed by Heidi Muller for the fall Lilly alum network newsletter which was published and distributed in early December 2010. To read full article, click here and be sure to go to page 4 for the...
IHIF event: “Social Media for the Life Sciences” on November 8, 2010 Come to this exciting event and learn more about how to use social media to promote, connect and influence your life science company’s customers or key stakeholders. Click here...
Pearl IRB attended and exhibited at the Site Solutions Summit held October 22-24 at the lovely Sandpearl resort in Clearwater. The event had a record number of attendees (more than 350), the sites attending were engaged, the sponsors and CROs who were there (not...
