๐”– Scriptorium
โœฆ   LIBER   โœฆ

๐Ÿ“

Validation of Active Pharmaceutical Ingredients, Second Edition

โœ Scribed by Ira R. Berry, Daniel Harpaz


Publisher
CRC Press
Year
2001
Tongue
English
Leaves
609
Edition
1
Category
Library

โฌ‡  Acquire This Volume

No coin nor oath required. For personal study only.

โœฆ Synopsis


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. Revised, updated, and expanded, this second edition includes new chapters addressing postapproval changes, technology transfer, international cGMP guidelines/FDA guidance progress, and facility inspection issues. The basic philosophy and principles of GMP and validation have not changed, but new terminology had been introduced, and old terminology had been better defined, improving the understanding of related concepts and principles. The book gives you a working knowledge of the regulatory process that will facilitate your organization's compliance with regulations


๐Ÿ“œ SIMILAR VOLUMES


Pharmaceutical Water: System Design, Ope
โœ William V. Collentro (Author) ๐Ÿ“‚ Library ๐Ÿ“… 2010 ๐Ÿ› CRC Press

<p>A major new work on all aspects of water, the most used raw material ingredient in the pharmaceutical and biotechnology industries-used as an excipient in pharmaceutical formulations, as a cleaning agent, and as a separately packaged product diluent.Drawing on the author`s extensive field experie

Pharmaceutical Biocatalysis-Chemoenzymat
โœ Peter Grunwald (Editor) ๐Ÿ“‚ Library ๐Ÿ“… 2019 ๐Ÿ› Jenny Stanford Publishing

<p>This volume provides an insight into the future strategies for commercial biocatalysis with a focus on sustainable technologies, together with chemoenzymatic and biotechnological approaches to synthesize various types of approved and new active pharmaceutical ingredients (APIs) via proven and lat

Active Pharmaceutical Ingredient Manufac
โœ Malhotra G.K. ๐Ÿ“‚ Library ๐Ÿ“… 2022 ๐Ÿ› Walter de Gruyter ๐ŸŒ English

The book reviews the history of current brand and generic business in pharmaceuticals manufacturing practices. Based on examples, the reader can interpolate, extrapolate and exploit mutual behavior (physical and chemical properties) of chemicals to design and commercialize processes that fulfi ll th

Active Pharmaceutical Ingredient Manufac
โœ Girish K. Malhotra ๐Ÿ“‚ Library ๐Ÿ“… 2022 ๐Ÿ› De Gruyter ๐ŸŒ English

<p>The book reviews the history of current brand and generic business in pharmaceuticals manufacturing practices. Based on examples, the reader can interpolate, extrapolate and exploit mutual behavior (physical and chemical properties) of chemicals to design and commercialize processes that fulfi ll

Active Pharmaceutical Ingredient Manufac
โœ Girish K. Malhotra ๐Ÿ“‚ Library ๐Ÿ“… 2022 ๐Ÿ› De Gruyter ๐ŸŒ English

<p>The book reviews the history of current brand and generic business in pharmaceuticals manufacturing practices. Based on examples, the reader can interpolate, extrapolate and exploit mutual behavior (physical and chemical properties) of chemicals to design and commercialize processes that fulfi ll