Sterile Drug Products: Formulation, Packaging, Manufacturing and Quality (Original Price GPB 130.00). Este artículo no está disponible.
Idioma: inglés
Editorial: T&F INDIA
Serie: Libro 55 de 80 - Drugs and the Pharmaceutical Sciences
- Tapa blanda
- Nuevo

Librería: SMASS Sellers, IRVING, TX, Estados Unidos de AmericaSMASS Sellers
Vendedor de 4 estrellas
Vendedor de IberLibro desde 22 de febrero de 2022
No disponible
Tapa blanda
Condición: Nuevo
EUR 55,29
Descripción del artículo del vendedor
Brand New, Softcover edition. This item may ship from the US or our Overseas warehouse depending on your location and stock availability.
N° de ref. del artículo SNTA-206200
- Título
- Sterile Drug Products: Formulation, Packaging, Manufacturing and Quality (Original Price GPB 130.00)
- Autor
- Michael J. Akers
- Editorial
- T&F INDIA
- Estado
- New
- Encuadernación
- Encuadernación de tapa blanda
- Idioma
- inglés
- ISBN 10
- 0367269635
- ISBN 13
- 9780367269630
- Serie
- Libro 55 de 80: Drugs and the Pharmaceutical Sciences
Sterile Drug Formulation, Packaging, Manufacturing, and Quality teaches the basic principles of the development and manufacture of high quality sterile dosage forms. 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 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 formClinical aspects, including administration, potential hazards, and biopharmaceutics of sterile products in a clinical setting.
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