Hygiene In Der Arzneimittelproduktion

Author: Michael Rieth
Publisher: John Wiley & Sons
ISBN: 352768476X
Size: 79.28 MB
Format: PDF
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Sichere und kontaminationsfreie Arzneimittel dank intelligenter Hygienekonzepte und Produktionsablï¿1⁄2ufe: Dieser neue Praxisleitfaden zu Grundlagen und Verfahren der hygienischen Pharmaproduktion deckt alle gï¿1⁄2ngigen ...

Der K Nig Aller Krankheiten

Author: Siddhartha Mukherjee
Publisher: Dumont Buchverlag
ISBN: 3832186220
Size: 14.20 MB
Format: PDF, Kindle
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Siddhartha Mukherjee widmet sich seinem Thema mit der Präzision eines Zellbiologen, mit der Kenntnis eines Historikers und mit der Passion eines Biografen.

Ein Und Zweidimensionale Nmr Spektroskopie

Author: Horst Friebolin
Publisher: John Wiley & Sons
ISBN: 3527334920
Size: 12.38 MB
Format: PDF, Docs
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Diese vollstandig uberarbeitete und aktualisierte Neuauflage des klassischen Lehrbuches beinhaltet neben den Grundlagen der NMR-Spektroskopie auch die der Spektreninterpretation.

Process Validation In Manufacturing Of Biopharmaceuticals

Author: Gail Sofer
Publisher: CRC Press
ISBN: 1420001655
Size: 60.51 MB
Format: PDF, ePub, Docs
View: 5806
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ANALYTICAL TESTING AND CONTROL STRATEGIES Analytical testing is one
of the most important programs in the biopharmaceutical industry. It starts with
raw materials and systems testing and continues through production, purification,
formulation, packaging, and storage (1). Analytical testing helps to monitor,
control, maintain, and ensure product quality and batch-to-batch consistency. The
quality and consistency depend not only on efficient process controls but also on
sound ...

Continuous Processing In Pharmaceutical Manufacturing

Author: Ganapathy Subramanian
Publisher: John Wiley & Sons
ISBN: 3527673709
Size: 10.77 MB
Format: PDF, ePub
View: 605
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The information and knowledge gained from pharmaceutical development
studies and manufacturing experience provide scientific understanding to
support the establishment of the design space, specifications, and manufacturing
controls. At a minimum, those aspects of drug substances, excipients, container
closure systems, and manufacturing processes that are critical to product quality
should be determined and control strategies justified. Critical formulation
attributes and process ...

Genetic Engineering News

Author:
Publisher:
ISBN:
Size: 59.40 MB
Format: PDF, Mobi
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Why Should We Spend Time on the Formulation Development of
Biopharmaceuticals? - Dr. Armin Bohmann, Bohman and Loosen The
preformulation and formulation of proteins prior to the first clinical and toxicology
studies as well as the planning of a formulation process and the information
required to start such a process is key for successful product development. The
presentation will focus on: - Impact of the structure of proteins on bioactivity, and
immunogenicity of the molecule.