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Paving the Way for Personalized Medicine: FDA’s Role in a New Era of Medical Product Development

This article is recommended for those in the dietary supplement and/or diagnostic/laboratory testing industry.

Article Discusses:

PERSONALIZED MEDICINE FROM A REGULATORY PERSPECTIVE
1. DEFINING PERSONALIZED MEDICINE
2. FDA’S UNIQUE ROLE AND RESPONSIBILITIES IN PERSONALIZED MEDICINE

DRIVING TOWARD AND RESPONDING TO SCIENTIFIC ADVANCES
1. BUILDING THE INFRASTRUCTURE TO SUPPORT PERSONALIZED MEDICINE
2. RECENT ORGANIZATIONAL EFFORTS

DEFINING AND CLARIFYING REGULATORY PATHWAYS AND POLICIES
1. ENSURING THE AVAILABILITY OF SAFE AND EFFECTIVE DIAGNOSTICS
2. PRODUCT INTERDEPENDENCY
3. PRODUCT LABELING
4. POST-MARKET SURVEILLANCE

ADVANCING REGULATORY SCIENCE IN SUPPORT OF PERSONALIZED MEDICINE
1. DEVELOPING REGULATORY STANDARDS, RESEARCH METHODS, AND TOOLS
2. CONDUCTING AND COLLABORATING IN RESEARCH

A NEW ERA OF MEDICAL PRODUCT DEVELOPMENT:
OPPORTUNITIES AND CHALLENGES AHEAD

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This entry was posted in Articles, Choosing Supplement Manufacturers, Dietary Supplement Industry Regulation, FDA, Personalized Lifestyle Medicine, Practice Management and tagged , . Bookmark the permalink. Follow any comments here with the RSS feed for this post.
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