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Upcoming Event: DA4S conference in Long Beach, CA February 17 – 18, 2016

The Diversity Alliance for Science (DA4S) conference will be held at the Marriott Long Beach Airport Hotel, in Long Beach, CA on February 17-18, 2016. DA4S is a non-profit organization focused on supporting, developing, and connecting with a diverse group of suppliers...

FDA and NIH receive more funding in 2016 from Omnibus Appropriations Bill

The House Appropriations Committee announced the Omnibus Appropriations bill providing the FDA and NIH more funds in the coming year. FDA will receive more funding in 2016 for: medical product safety initiatives Combating Antibiotic Resistant Bacteria (CARB)...

Pearl Pathways is proud to sponsor Indiana Life Sciences Collaboration Conference Series

Pearl Pathways continues to be a proud sponsor of the 2015-2016 Indiana Life Sciences Collaboration Conference Series, presented by the Kelley School’s Center for the Business of Life Sciences. This is an excellent forum bringing together key players in Indiana’s life...

Pre-screening CRAs for competency may help CROs’ efforts to hire and retain quality talent

Dan Stanton of Outsourcing-Pharma recently published an article on the topic of Clinical Research Associates (CRAs) who have been able to demand higher and higher salaries and bonuses lately. Retaining quality talent has been problematic for companies, and they are...

FREE Webinar on The Year Ahead in Asia Pacific Regulations from Pearl Pathways partner, Brandwood Medical – January 19th

Next Tuesday, learn about the emerging trends in Asia Pacific regulations in a webinar presented by Principal Consultant, Arthur Brandwood of Brandwood Biomedical.  Click here for your FREE registration.  Learn more about Brandwood Medical here.
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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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