Biopharmaceutical Manufacturing, Volume 1: Regulatory Processes. Este artículo no está disponible.
Idioma: inglés
Editorial: Institute of Physics Publishing, 2022
- Tapa dura
- Nuevo
Librería: THE SAINT BOOKSTORE, Southport, Reino UnidoTHE SAINT BOOKSTORE
Vendedor de AbeBooks desde el 14 de junio de 2006
Condición: Nuevo
EUR 215,43
Descripción del artículo del vendedor
This item is printed on demand. New copy - Usually dispatched within 5-9 working days.
N° de ref. del artículo C9780750331739
- Título
- Biopharmaceutical Manufacturing, Volume 1: Regulatory Processes
- Autor
- Professor Sarfaraz K. Niazi
- Editorial
- Institute of Physics Publishing
- Año de publicación
- 2022
- Estado
- New
- Encuadernación
- Hardback
- Idioma
- inglés
- ISBN 10
- 0750331739
- ISBN 13
- 9780750331739
- Peso del artículo
- 209 gramos
This volume covers the regulatory processes involved in producing a GMP (Good Manufacturing Practice) biopharmaceutical product for commercial distribution, including areas of current GMP, registration, and legal and ethical considerations. Emerging trends in the technology and regulatory compliance are also discussed, with advice on establishing efficient manufacturing facilities. Intended for practitioners in the commercial biopharmaceutical manufacturing industry, the text is an ideal resource for practitioners looking to develop their ability to manufacture biopharmaceutical products at a large scale.
“Sinopsis” puede pertenecer a otra edición de este título.
Acerca del autor
Sunitha Lokesh is the director of biomanufacturing operations at Pharmaceutical Scientist Inc., where she leads the identification and technology development of biopharmaceutical products. She has over 10 years of experience in developing biopharmaceuticals, from the cell line to process validation.
“Acerca de” puede pertenecer a otra edición de este título.