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KISS Your Pharma Content Problems Goodbye

Tracy Rockney J.D.

Co-founder & Managing Partner at OneSource Regulatory

In this concise and insightful white paper, pharmaceutical industry veteran Tracy Rockney provides a candid assessment of the current medical information model. With observations based on 20 years of industry experience, Rockney casts a critical eye on today’s inefficient medical content management and offers a path forward to reduce cost and regulatory risk and bring products to market faster.

Anyone involved in the assessment and selection of content management systems will want to read this important paper.

Act now to obtain your free copy of KISS Your Pharma Content Problems Goodbye.


BIOGRAPHY:

Tracy Rockney J.D. Tracy Rockney is a respected regulatory leader with more than 20 years of experience in the pharmaceutical industry. She is the Co-founder and Managing Partner at OneSource Regulatory, a consulting firm specializing in Regulatory Advertising & Promotion, Medical Review, Labeling Development and Healthcare Compliance. Her senior regulatory management experience included her role as Vice President, Regulatory Affairs, Global Labeling, Advertising & Promotion, Regulatory Policy & Intelligence at AbbVie (formerly Abbott Pharmaceuticals), Senior Director, Global Regulatory Affairs at Shire Pharmaceuticals, Director, Regulatory Affairs at Wyeth, and Director, Global Regulatory Strategy at Pfizer.

Tracy received her Juris Doctor from Washburn University School of Law, and her Bachelor of Arts from the University at Albany, State University of New York, Rockefeller College of Public Affairs & Policy. Tracy is a board advisor and Regulatory Officer in Residence for Doctor Evidence, a specialty software platform and services company that transforms clinical studies, drug labeling and epidemiological.


ABOUT OUTSOURCED REGULATORY AND MEDICAL REVIEW
RESOURCES CUSTOMIZED TO YOUR NEEDS

OneSource Regulatory, OSR, is focused on providing expertise in the areas of Regulatory and Medical advertising/promotion review, the development of regulatory drug product labeling, and Commercial Compliance. Utilizing expertise from decades of proven industry experience, OSR provides expert resources selected by people who have actually held the job inside pharma companies.

OSR’s mission is to bring innovation to a dormant industry, to provide a reliable & dependable team of experts, and to provide regulatory/medical services and advice at the simple click of a button.