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Gretchen Bowker moderates the June 22 morning session of the AFDO event in Indianapolis

We are pleased to announce that our own, Gretchen Bowker, will be moderating the Association of Food and Drug Officials (ADFO) meeting today June 22nd. The AFDO is holding their event this week from June 20th to June 24th in Indianapolis at the Sheraton Indianapolis...

Join Pearl Pathways at the 5th Annual Clinical Affairs and Regulatory Approvals for Diagnostics Conference

Pearl Pathways is excited to be attending and presenting at the Annual Clinical Affairs & Regulatory Approvals for Diagnostics Conference next week in Alexandria, VA. This conference provides a forum for discussion on the challenges regulators face and strategies...

American Chemical Society national meeting features Gretchen Bowker, COO

Gretchen Miller Bowker, Pearl IRB COO, will be a featured speaker at the ACS annual meeting. The conference will be held  September 8 – 12th, 2013. To register and see the full agenda, click here. Date/time:                                   September 9th, 9:45...

IEDC awards Pearl Pathways incentive package of tax credits and training grants

Today, the IEDC released the below press release: INDIANAPOLIS (Jan. 29, 2013) – Pearl IRB, LLC d/b/a Pearl Pathways, a life sciences product development and regulatory consultant company, announced plans today to expand its operations here, creating up to 38 new jobs...

IBJ Biofutures magazine feature: “Pearl IRB Expands to Offer New Services”

Check out the 2012 IBJ Biofutures article covering our expansion last year to Pearl Pathways using this link.  You will need to page through to the article on page 33. Key quotes include: “Our clients shaped the direction of our future growth,” says Diana Caldwell,...
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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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