Handbook of Pharmaceutical Manufacturing Formulations
Volume Two, Uncompressed Solid Products
Providing methodologies that can serve as a reference point for new formulations, the second volume covers uncompressed solids,
which include formulations of powders, capsules, powders ready for reconstitution, and other similar products. Les mer
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Vår pris:
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Providing methodologies that can serve as a reference point for new formulations, the second volume covers uncompressed solids,
which include formulations of powders, capsules, powders ready for reconstitution, and other similar products.
Highlights from Uncompressed Solid Products, Volume Two include:
the fundamental issues of good manufacturing practices
formulations for more than 400 pharmaceutical products, including currently approved products and innovative products such as small proteins, instantly liquifiable powders, and nanoparticles
access to US FDA guidelines, as well as all major guidelines around the world
identification and inclusion of the most often approved capsules and powders in the US
Highlights from Uncompressed Solid Products, Volume Two include:
the fundamental issues of good manufacturing practices
formulations for more than 400 pharmaceutical products, including currently approved products and innovative products such as small proteins, instantly liquifiable powders, and nanoparticles
access to US FDA guidelines, as well as all major guidelines around the world
identification and inclusion of the most often approved capsules and powders in the US
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Utgitt:
2019
Forlag: CRC Press
Innbinding: Paperback
Språk: Engelsk
Sider: 388
ISBN: 9780367385217
Utgave: 2. utg.
Format: 28 x 21 cm
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- VURDERING
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Gi vurdering
Les vurderinger
REGULATORY AND MANUFACTURING GUIDELINES: U.S. FDA Good Manufacturing Practices. GMP Audit Template, EU Guidelines. Guideline
on the Common Technical Document for the Registration of Pharmaceuticals for Human Use. Process Validation: General Principles
and Practices. Bioequivalence Regulatory Compliance. Bioequi valence Regulatory Review Process and Audit. EU Guidelines to
Good Manufacturing Practice. Preapproval Inspections. Formulation Factors in Uncompressed Dosage Forms. Bioequivalence Testing
Protocols. Dissolution Testing of Uncompressed Solid Dosage Forms. Approved Excipients in Uncompressed Solid Dosage Forms.
MANUFACTURING FORMULATIONS: Uncompressed Solids Formulations.
Niazi, Sarfaraz K.