Thriving Through Turmoil: Managing Sales and Marketing Regulation of the Medical Device Industry

April 01, 2010

By Jeff Campbell


The Pharmaceutical Research and Manufacturers of America (PhRMA) Code, Office of the Inspector General (OIG) Guidance and the Prescription Drug Marketing Act,1 are just some of the federal and industry laws and guidances with which pharmaceutical companies and their representatives must comply in order to market pharmaceutical products in the United States.

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