Validation Active Pharmaceutical Ingredients (17 results)

Condition: New. Brand New. Soft Cover International Edition. Different ISBN and Cover Image. Priced lower than the standard editions which is usually intended to make them more affordable for students abroad. The core content of the book is generally the same as the standard edition. The country selling restrictions may be printed on the book but is no problem for the self-use. This Item maybe shipped from US or any other country as we have multiple locations worldwide.…

Condition: New. Brand New! Fast Delivery This is an International Edition and ship within 24-48 hours. Deliver by FedEx and Dhl, & Aramex, UPS, & USPS and we do accept APO and PO BOX Addresses. Order can be delivered worldwide within 6-10 days and we do have flat rate for up to 2LB. Extra shipping charges will be requested if the Book weight is more than 5 LB. This Item May be shipped from India, United states & United Kingdom. Depending on your location and availability.…

N.A. Condition: New. ISBN:9781574911190,Territorial restriction maybe printed on the book. This is an Int'l edition, ISBN and cover may differ from US edition, Contents same as US edition.

Taschenbuch. Condition: Neu. Analytical Method Development and Validation | Development and Validation of Analytical Methods for Active Pharmaceutical Ingredients in Pharmaceutical Dosage Form | Deepali Chavan (u. a.) | Taschenbuch | Englisch | LAP Lambert Academic Publishing | EAN 9783838398471 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.…

hardcover. Condition: New. In shrink wrap. Looks like an interesting title.

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Hardcover. Condition: Brand New. 2nd edition. 618 pages. 9.50x7.25x1.50 inches. In Stock.

Condition: New. pp. xxix + 588 Figures This item is printed on demand.

Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - A number of drugs are introduced in the market every year, also many new fixed dose combinations of already individually approved drugs are formulated with an aim to achieve better therapeutic efficacy. Pharmaceutical products formulated with more than one drug, typically referred to as combination products, are intended to meet previously unmet patients need by combining the therapeutic effects of two or more drugs in one product. These combination products can present daunting challenges to the analytical chemist responsible for the development and validation of analytical methods Many times few combinations do not have any official methods for simultaneous analysis of their active pharmaceutical ingredients . This is because there is a time lag between the introduction of the drug into the market and its inclusion in the pharmacopoeias. Hence it becomes necessary to develop newer analytical methods for routine analysis of these drugs which will help to ensure the identity, purity, potency and performance of the drugs in the dosage forms. …

Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Ira R. BerryMuch has happened in the area of bulk pharmaceutical good manufacturing practice (GMP) and validation since the first publication of Validation of Active Pharmaceutical Ingredients. Revised, updated, and expanded, this second edition include.…

Buch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Much has happened in the area of bulk pharmaceutical good manufacturing practice (GMP) and validation since the first publication of Validation of Active Pharmaceutical Ingredients. The second edition is fully revised, updated, and expanded to include new chapters addressing postapproval changes, technology transfer, international cGMP guidelines/FDA guidance progress, and facility inspection issues. New terminology has been introduced and the old terminology has been better defined to improve the understanding of related concepts and principles. With this book, readers gain a working knowledge of the regulatory process that will facilitate their organization's compliance.…