Handbook of Pharmaceutical Manufacturing Formulations

Volume One, Compressed Solid Products
2. New Auflage 2009
ISBN: 978-1-4200-8116-9
Verlag: Taylor & Francis Inc

Buch, Englisch, 648 Seiten, Format (B × H): 222 mm x 289 mm, Gewicht: 2124 g

The largest category of pharmaceutical formulations, comprising almost two-thirds of all dosage forms, compressed solids present some of the greatest challenges to formulation scientists. The first volume, Compressed Solid Products, tackles these challenges head on.
Highlights from Compressed Solid Products, VolumeOne include:

formulations for more than 200 of the most widely used drugs for all types of release profiles, offering formulators a rare opportunity to start with an optimal composition
the essentials of what you need to be aware of when establishing a manufacturing process based on the formulations presented
identification and inclusion of the most popular prescription products, a critical list for the selection of products

Zielgruppe

Pharmaceutical manufacturers, and quality assurance and production personnel.

Autoren/Hrsg.

Niazi, Sarfaraz K.

Fachgebiete

• Wirtschaftswissenschaften Wirtschaftssektoren & Branchen Fertigungsindustrie Pharmaindustrie

Inhaltsverzeichnis

Bioequivalence Testing Rationale and Principles. Bioequivalence Testing Protocols-FDA-Compressed Dosage Forms. GMP Audit Template, EU Guidelines. Guidance on Formulating Compressed Solids. Appendix I: Dissolution Testing Requirements of Compressed Dosage Forms. Appendix II: Approved Excipients in Compressed Solid Dosage Forms.