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Precision for Medicine Adds Regulatory Expertise To Support Next Generation Medicines
Date:5/30/2013

CHEVY CHASE, Md., May 30, 2013 /PRNewswire/ -- Precision for Medicine, Inc., ("Precision"), the specialized scientific services company formed in 2012 to support next generation medical products, today announced the appointment of three key executives, significantly increasing the breadth of its regulatory and commercialization services. The addition of these executives and their teams expands and enhances Precision's ability to support life science innovators as they work to address value, effectiveness, and patient access for next generation medicines.  

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"Developers of diagnostic technologies – particularly companion diagnostics that support a new generation of biopharmaceuticals– are looking for a specific set of services as they work to guide their products to market," said Precision co-founder, Mark P. Clein . "The leadership team we have assembled at Precision for Medicine provides a unique combination of industry experience and scientific expertise to help guide all aspects of diagnostic and product development, from strategy to regulatory affairs, and from clinical trial design to commercialization."

Judi Smith , M.S., M.T. (ASCP) has been appointed Vice President, In Vitro Diagnostics Regulatory and Quality and will lead Precision's regulatory support services for diagnostic products, including companion diagnostics for next generation biopharmaceuticals. In this role, Ms. Smith will help clients guide diagnostics products from initial development through regulatory submission, review, and approval. Ms. Smith, who is currently the president of the Association of Medical Diagnostic Manufacturers, has worked in regulatory and quality sciences and clinical devel
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SOURCE Precision for Medicine, Inc.
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