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Don’t miss the IMDMC “Effectively Managing Multi-Center Trials”- January 27th, 2011

Gretchen Miller Bowker, COO, Pearl IRB is speaking at the IMDMC regulatory roundtable “Effectively Managing Multi-Center Trials” – REGISTER NOW! Speakers: Jennifer L. Kerr, VP of Operations MED Institute, Inc. Jenna Sallee, Executive Director...

Gretchen Miller Bowker, COO, Pearl IRB speaks at the January 11th ASQ meeting

Come join us at an event hosted by the Indianapolis Section of ASQ  for their January 2011 Dinner Meeting.  Gretchen Bowker, COO of Pearl IRB will present “IRBs Past and Future” Date: Tuesday, 11 Jan 2011 5:30 PM – 7:30 PM – EasternTime...

Pearl IRB receives national certification as a Women’s Business Enterprise

On November 18, 2010, Pearl IRB, a company providing clinical trial research institutional review board services and other key clinical trial assistance, received national certification as a Women’s Business Enterprise by the Great Lakes Women’s Business Enterprise...

Pearl IRB speaking on panel and exhibiting at the ACRP Excellence in Clinical Research Fall Symposium – REGISTER NOW!

Don’t miss the Circle City ACRP Event held on November 6, 2010  Who should attend: All personnel who are involved in or planning to be involved in clinical research. This conference is targeted for both new and experienced clinical research professionals...

Pearl IRB attended Site Solutions Summit October 22-24 in Clearwater, Florida

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...
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Pearl Pathways is a comprehensive life science product development services company. Every day we strive to provide our customers top quality service, unyielding ethics, and efficient services through our team of experts. Pearl Pathways supports biopharmaceutical, medical device, and diagnostic companies as well as life science service providers with clinical, regulatory, and quality compliance needs. Our full-service central IRB supports all aspects of human research.

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