Active Pharmaceutical Ingredients: Development, Manufacturing, and Regulation, Second Edition: 205 (Drugs and the Pharmaceutical Sciences) - Hardcover

Hardcover

ISBN 10: 1439803366 ISBN 13: 9781439803363

Verlag: CRC Press, 2009

Inhaltsangabe

Unusual book

Über diesen Titel

Reseña del editor:

To successfully bring an Active Pharmaceutical Ingredient (API) to market, many steps must be followed to ensure compliance with governmental regulations. Active Pharmaceutical Ingredients is an unparalleled guide to the development, manufacturing, and regulation of the preparation and use of APIs globally.

Topics include:

• Safety, efficacy, and environmental/regulatory requirements
• Analysis of the recent movement of API manufacturing from the U.S. and Europe to countries such as India and China
• The FDA's intensified foreign inspection program
• Multi-use and flexible design facilities
• The shift from maintenance scheduling to built-in reliability

This second edition focuses on the quality control regulations for APIs that have been added or amended since the first edition. These updates help ensure that pharmaceutical professionals and drug manufacturers meet the established and required guidelines set forth by the United States and international regulatory agencies.

Reseña del editor:

Active Pharmaceutical Ingredients is an unparalleled guide to the development, manufacturing, and regulation of the preparation and use of Active Pharmaceutical Ingredients (APIs) globally.

This Second Edition brings you up-to-date with the quality control regulations for APIs that have been added or amended since the first edition. These updates help ensure that pharmaceutical professionals and drug manufacturers meet the established and required guidelines set forth by the US and international regulatory industries.

New features include:

• chapters on safety, efficacy, and environmental/regulatory requirements
• analysis of the recent movement of API manufacturing from the US and Europe to countries such as India and China
• discussions on both US and international regulatory requirements
• information about the FDA’s intensified foreign inspection program
• data on multi-use and flexible design facilities
• the shift from maintenance scheduling to built-in reliability

Über diese Auflage

• Verlag: CRC Press
• Erscheinungsdatum: 2009
• ISBN 10: 1439803366
• ISBN 13: 9781439803363
• Einband: Tapa dura
• Auflage: 2
• Anzahl der Seiten: 456
• Herausgeber: Nusim Stanley