Validation of Active Pharmaceutical Ingredients

Validation of Active Pharmaceutical Ingredients, Second Edition  eBooks & eLearning

Posted by DZ123 at Feb. 26, 2016
Validation of Active Pharmaceutical Ingredients, Second Edition

Ira R. Berry, Daniel Harpaz, "Validation of Active Pharmaceutical Ingredients, Second Edition"
English | 2001 | ISBN: 1574911198 | PDF | pages: 609 | 16,5 mb
Active Pharmaceutical Ingredients, Second Edition: Development, Manufacturing, and Regulation

Stanley Nusim, "Active Pharmaceutical Ingredients, Second Edition"
Informa Healthcare | ISBN: 1439803366 | 2009 | PDF | 355 pages | 3,18 mb

Active Pharmaceutical Ingredients is an unparalleled guide to the development, manufacturing, and regulation of the preparation and use of Active Pharmaceutical Ingredients (APIs) globally.
Active Pharmaceutical Ingredients: Development, Manufacturing, and Regulation by Stanley Nusim [Repost]

Active Pharmaceutical Ingredients: Development, Manufacturing, and Regulation (Drugs and the Pharmaceutical Sciences) by Stanley Nusim
CRC Press | May 25, 2005 | English | ISBN: 8131727246 | 341 pages | PDF | 8 MB

Focusing on the three most critical components that successfully bring an API to market-process development, manufacturing, and governmental regulation and approval-this reference serves as a step-by-step guide to the planning and clear understanding of the bulk manufacturing of APIs. This guide offers current and timely discussions of the process development cycle, design engineering, the approval process, quality control and assurance, and validation, as well as plant manufacturing activities including materials management, maintenance, and safety.
Active Pharmaceutical Ingredients by Stanley Nusim [Repost]

Active Pharmaceutical Ingredients: Development, Manufacturing, and Regulation, Second Edition (Drugs and the Pharmaceutical Sciences) by Stanley Nusim
English | Dec 23, 2009 | ISBN: 1439803366 | 452 Pages | PDF | 24 MB

To successfully bring an Active Pharmaceutical Ingredient (API) to market, many steps must be followed to ensure compliance with governmental regulations.

Active Pharmaceutical Ingredients (Repost)  

Posted by DZ123 at Sept. 3, 2014
Active Pharmaceutical Ingredients (Repost)

Stanley Nusim, "Active Pharmaceutical Ingredients: Development, Manufacturing, and Regulation"
English | 2005 | ISBN: 082470293X | PDF | pages: 341 | 8,7 mb
Micro/Nano Encapsulation of Active Food Ingredients (ACS Symposium) (repost)

Qingrong Huang, "Micro/Nano Encapsulation of Active Food Ingredients (ACS Symposium)"
English | 2009 | ISBN: 0841269645 | PDF | 329 pages | 35,4 MB

This book highlights recent innovation in encapsulation and controlled release technologies, as well as design principle of novel food delivery systems. In addition, it also provided some new directions and opportunities that can arise from the development of new nanostructured biomaterials for the fabrication of delivery vehicles and carriers for active food ingredients.

Active Pharmaceutical Ingredients: Development, Manufacturing, and Regulation  eBooks & eLearning

Posted by maxxum at July 26, 2006
36322
Stanley Nusim (Editor), «Active Pharmaceutical Ingredients: Development, Manufacturing, and Regulation»
Informa Healthcare | ISBN 082470293X | (May 25, 2005) | PDF | 2.5 Mb | 368 pages

Process Understanding: For Scale-Up and Manufacture of Active Ingredients

Ian Houson - Process Understanding: For Scale-Up and Manufacture of Active Ingredients
Published: 2011-05-23 | ISBN: 3527325840 | PDF | 370 pages | 3 MB
Encapsulation Technologies for Active Food Ingredients and Food Processing (repost)

Encapsulation Technologies for Active Food Ingredients and Food Processing
Springer; 1st Edition | November 16, 2009 | ISBN-10: 1441910077 | 400 pages | PDF | 10.7 Mb

Consumers prefer food products that are tasty, healthy and convenient. Encapsulation is an important way to meet these demands by delivering food ingredients at the right time and right place.
Global Specification and Validation of Embedded Systems: Integrating Heterogeneous Components

Global Specification and Validation of Embedded Systems: Integrating Heterogeneous Components
Springer Netherlands | December 28, 2009 | ISBN-10: 904817550X | 160 pages | PDF | 3.36 MB

Global modelling and validation is required to master the design of systems made of heterogeneous components. These systems are now omnipresent in our life, and they may be found in several domains such as communications (ex. mobile terminals, optical switches), health (e.g. cardiac stimulators, cochlear implants), transportation (ex. automotive and aeronautical), etc. The main difficulties for their design are modelling and validation of the interactions between different components (hardware, software, analogue, RF, optical and micro-mechanical).