Drug compounding : background, issues and FDA oversight /

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 licen...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Bram, Martti (Editor )
Formato: Electrónico eBook
Idioma:Inglés
Publicado: New York : Nova Publishers, [2014]
Colección:Pharmacology-research, safety testing, and regulation series.
Temas:
United States. > Food and Drug Administration.
Drugs > Dosage forms > United States > Evaluation.
Pharmaceutical industry > United States > Quality control.
Public health > Standards > United States.
Products liability > Drugs > United States.
Médicaments > Formes pharmaceutiques > États-Unis > Évaluation.
Industrie pharmaceutique > États-Unis > Qualité > Contrôle.
Santé publique > Normes > États-Unis.
Responsabilité du fait des produits > Médicaments > États-Unis.
MEDICAL > Pharmacology.
Pharmaceutical industry > Quality control.
Products liability > Drugs.
Public health > Standards.
United States.
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