Description

Book Synopsis
Compounding has been traditionally defined as a process where a pharmacist or a physician combines, mixes, or alters ingredients to create a medication tailored to the needs of an individual patient. Traditionally compounded drugs (CDs) are made in response to an individual prescription from a licensed health provider in the context of a pharmacist''s and health care professional''s relationship with a specific patient. This book provides background information on CDs and non-traditional compounding pharmacies relevant to policy discussions. This book will also examine the FDA''s regulation of drug compounding and will discuss relevant legal authorities. Specifically, the status of FDA''s authority to oversee drug compounding, and the gaps, if any, between state and federal authority will be discussed, as well as how FDA has used its data and authority to oversee drug compounding, and the actions taken or planned by states or national pharmacy organisations to improve oversight of drug compounding.

Drug Compounding: Background, Issues & FDA

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    A Hardback by Martti Bram

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      Book details

      Publisher Nova Science Publishers Inc
      Published 14 May 2014
      ISBN-13 9781631173608
      978-1631173608
      ISBN-10 163117360X
      Also in:
      Pharmacology

      Description

      Book Synopsis
      Compounding has been traditionally defined as a process where a pharmacist or a physician combines, mixes, or alters ingredients to create a medication tailored to the needs of an individual patient. Traditionally compounded drugs (CDs) are made in response to an individual prescription from a licensed health provider in the context of a pharmacist''s and health care professional''s relationship with a specific patient. This book provides background information on CDs and non-traditional compounding pharmacies relevant to policy discussions. This book will also examine the FDA''s regulation of drug compounding and will discuss relevant legal authorities. Specifically, the status of FDA''s authority to oversee drug compounding, and the gaps, if any, between state and federal authority will be discussed, as well as how FDA has used its data and authority to oversee drug compounding, and the actions taken or planned by states or national pharmacy organisations to improve oversight of drug compounding.

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