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The Mission of the Alliance, with the support of its members, is to improve the understanding of the PDMA and other laws and regulations governing pharmaceutical samples and to improve the efficiency and effectiveness of sample accountability programs. Congress passed the Prescription Drug Marketing
Act of 1987 (PDMA) to help ensure our drug products would be safe
and effective, and to lessen the risk that counterfeit, adulterated,
misbranded, or expired drugs would enter America’s drug supply chain. The PDMA Alliance Inc. is the industry voice of PDMA compliance professionals. Our members are dedicated to improving the understanding of the PDMA by the pharmaceutical industry, and to strengthening the efficiency and effectiveness of the sample accountability programs we administer. The Alliance serves as the industry’s focal point for learning, exchanging ideas, and networking on issues related to PDMA compliance. We work closely with the U.S. Food and Drug Administration (FDA), and with our members, to continually improve our business and security practices. Examples of some Alliance initiatives, either planned or in progress, include the development of standardized loss/theft reports required under the PDMA; implementation of a uniform, web-based reporting system; and the development of industry “best practice” guidelines and a self-audit program for our members. There are two aspects of The PDMA Alliance that characterize the workings of the organization:
Interested in becoming a member? Want more information about The PDMA Alliance
Inc.?
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