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portada Cleaning Validation Manual: A Comprehensive Guide for the Pharmaceutical and Biotechnology Industries (en Inglés)
Formato
Libro Físico
Editorial
Idioma
Inglés
N° páginas
608
Encuadernación
Tapa Dura
Dimensiones
25.4 x 18.3 x 3.8 cm
Peso
1.22 kg.
ISBN
9781439826607
ISBN13
9781439826607

Cleaning Validation Manual: A Comprehensive Guide for the Pharmaceutical and Biotechnology Industries (en Inglés)

Syed Imtiaz Haider (Autor) · CRC Press · Tapa Dura

Cleaning Validation Manual: A Comprehensive Guide for the Pharmaceutical and Biotechnology Industries (en Inglés) - Haider, Syed Imtiaz

Libro Físico

$ 205.990

$ 374.530

Ahorras: $ 168.540

45% descuento
  • Estado: Nuevo
  • Quedan 100 unidades
Origen: Reino Unido (Costos de importación incluídos en el precio)
Se enviará desde nuestra bodega entre el Martes 16 de Julio y el Viernes 26 de Julio.
Lo recibirás en cualquier lugar de Chile entre 1 y 3 días hábiles luego del envío.

Reseña del libro "Cleaning Validation Manual: A Comprehensive Guide for the Pharmaceutical and Biotechnology Industries (en Inglés)"

During the past decades, enormous progress and enhancement of pharmaceutical manufacturing equipment and its use have been made. And while there are support documents, books, articles, and online resources available on the principles of cleaning and associated processing techniques, none of them provides a single database with convenient, ready-to-use training tools. Until now. Cleaning Validation Manual: A Comprehensive Guide for the Pharmaceutical and Biotechnology Industries elucidates how to train the man power involved in development, manufacturing, auditing, and validation of bio pharmaceuticals on a pilot scale, leading to scale-up production.With over 20 easy-to-use template protocols for cleaning validation of extensively used equipments, this book provides technical solutions to assist in fulfilling the training needs of finished pharmaceutical manufacturers. Drawing on the authors' more than two decades of experience in the pharmaceutical and biotech industries, the text offers hands-on training based on current approaches and techniques. The book does not merely provide guidelines or thought processes, rather it gives ready-to-use formulas to develop Master Plan, SOPs, and validation protocols. It includes cleaning procedures for the most commonly used equipment in various manufacturing areas and their sampling points, using a pharmaceutical manufacturing site with both sterile and non-sterile operations as the case facility. It also provides the training guidelines on downloadable resources to enable users to amend or adopt them as necessary.Grounded in practicality, the book's applicability and accessibility set it apart. It can be used as a guide for implementing a cleaning validation program on site without the help of external consultants, making it a resource that will not be found collecting dust on a shelf, but rather, referred to again and again.

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