Sterile Drug Products

Author: Michael J. Akers
Edition: 1
Publisher: CRC Press
Binding: Hardcover
ISBN: 0849339936

Sterile Drug Products: Formulation, Packaging, Manufacturing and Quality (Drugs and the Pharmaceutical Sciences)

Sterile Drug Products: Formulation, Packaging, Manufacturing, and Quality teaches the basic principles of the development and manufacture of high quality sterile dosage forms. Medical books Sterile Drug Products. The author has 38 years of experience in the development and manufacture of sterile dosage forms including solutions, suspensions, ophthalmics and freeze dried products. This book is based on the courses he has delivered for over three decades, to over 3000 participants, and is intended to remain relevant for the indefinite future even as new technologies and new applications of old technologies become common.

This is an ideal reference book for those working directly and indirectly with sterile dosage forms, be it product development (formulation, package, process, analytical), manufacturing, quality control, quality assurance, regulatory, purchasing, or project management. This book is also intended as an educational resource for the pharmaceutical and biopharmaceutical industry and pharmacy schools, providing basic knowledge and principles in four main areas of parenteral science and technology:

• Product development, including formulation, packaging, and process development Medical books Sterile Drug Products: Formulation, Packaging, Manufacturing, And Quality By. Store Search search Title, ISBN and Author Sterile Drug Products: Formulation, Packaging, Manufacturing, and Quality by Michael J. Akers Estimated delivery 4-14 business days Format Hardcover Condition Brand New Supplying the latest research on the formulation, manufacture, quality control, and regulation of pharmaceuticals, biopharmaceuticals, and related products, this reference contains up-to-the-minute chapters on contamination control, facilities management, inspection, distribution, GMP,
  
  

  Download link for Sterile Drug Products: Formulation, Packaging, Manufacturing And Quality Akers,

  
  Store Search search Title, ISBN and Author Sterile Drug Products: Formulation, Packaging, Manufacturing, and Quality by Michael J. Akers Estimated delivery 4-14 business days Format Hardcover Condition Brand New Supplying the latest research on the formulation, manufacture, quality control, and regulation of pharmaceuticals, biopharmaceuticals, and related products, this reference contains up-to-the-minute chapters on contamination control, facilities management, inspection, distribution, GMP,
  
  
  
  New Hardcover.
  
  
  
  This book is written by Michael K. Akers Published by Taylor & Francis Group In 2010 and is available in Hardback POD will be shipped in 12 Days.
  
  
  
  TheNile.com.au About FAQ Payment Delivery Contact Us 1800-987-323 Sterile Drug Products: Formulation, Packaging, Manufacturing, and Quality (English) by Michael J. Akers Format Hardcover Condition Brand New Language English Supplying the latest research on the formulation, manufacture, quality control, and regulation of pharmaceuticals, biopharmaceuticals, and related products, this reference contains up-to-the-minute chapters on contamination control, facilities management, inspection, distrib
  
  
  
  
  

  Medical Book Sterile Drug Products

  
  
  The author has 38 years of experience in the development and manufacture of sterile dosage forms including solutions, suspensions, ophthalmics and freeze dried products. This book is based on the courses he has delivered for over three decades, to over 3000 participants, and is intended to remain relevant for the indefinite future even as new technologies and new applications of old technologies become common.

  This is an ideal reference book for those working directly and indirectly with sterile dosage forms, be it product development (formulation, package, process, analytical), manufacturing, quality control, quality assurance, regulatory, purchasing, or project management. This book is also intended as an educational resource for the pharmaceutical and biopharmaceutical industry and pharmacy schools, providing basic knowledge and principles in four main areas of parenteral science and technology:

  • Product development, including formulation, packaging, and process development.
  • Manufacturing, including basic teaching on all the primary unit operations involved in preparation of sterile products and the underlying importance of contamination control.
  • Quality and regulatory, including the application of good manufacturing practice regulations, aseptic processing guidelines, and unique quality control testing methods for the sterile dosage form
  • Clinical aspects, including administration, potential hazards, and biopharmaceutics of sterile products in a clinical setting.