FDA Drug Approval: Elements and Considerations (Pharmacology-Research, Safety Testing and Regulation)

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9781622570911: FDA Drug Approval: Elements and Considerations (Pharmacology-Research, Safety Testing and Regulation)
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The Food and Drug Administration (FDA) oversees the approval and regulation of drugs entering the U.S. market. Two regulatory frameworks support the FDA's review of prescription drugs. First, FDA reviews the safety and effectiveness of new drugs that manufacturers wish to market in the United States; this process is called pre-market approval or pre-approval review. Second, once a drug has passed that threshold and is FDA-approved, FDA acts through its post-market or post-approval regulatory procedures. This book is a primer on drug approval and regulation. It describes how drugs are approved and come to market, including the FDA's role in that process and the FDA and industry roles once drugs are on pharmacy shelves.

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Book Description Nova Science Publishers Inc, United States, 2012. Hardback. Condition: New. UK ed.. Language: English . Brand New Book. The Food and Drug Administration (FDA) oversees the approval and regulation of drugs entering the U.S. market. Two regulatory frameworks support the FDA s review of prescription drugs. First, FDA reviews the safety and effectiveness of new drugs that manufacturers wish to market in the United States; this process is called pre-market approval or pre-approval review. Second, once a drug has passed that threshold and is FDA-approved, FDA acts through its post-market or post-approval regulatory procedures. This book is a primer on drug approval and regulation. It describes how drugs are approved and come to market, including the FDA s role in that process and the FDA and industry roles once drugs are on pharmacy shelves. Seller Inventory # AAG9781622570911

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Book Description Nova Science Publishers Inc, United States, 2012. Hardback. Condition: New. UK ed.. Language: English . Brand New Book. The Food and Drug Administration (FDA) oversees the approval and regulation of drugs entering the U.S. market. Two regulatory frameworks support the FDA s review of prescription drugs. First, FDA reviews the safety and effectiveness of new drugs that manufacturers wish to market in the United States; this process is called pre-market approval or pre-approval review. Second, once a drug has passed that threshold and is FDA-approved, FDA acts through its post-market or post-approval regulatory procedures. This book is a primer on drug approval and regulation. It describes how drugs are approved and come to market, including the FDA s role in that process and the FDA and industry roles once drugs are on pharmacy shelves. Seller Inventory # AAG9781622570911

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KING T.I.
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EDITED BY: TIMOTHY I KING, THOMAS R BAKER .
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Book Description Nova Science Publishers, Inc (US), 2012. Hardback. Condition: NEW. 9781622570911 This listing is a new book, a title currently in-print which we order directly and immediately from the publisher. For all enquiries, please contact Herb Tandree Philosophy Books directly - customer service is our primary goal. Seller Inventory # HTANDREE0164742

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