Parenteral Medications • Volume 2 provides thorough coverage of parenteral dosage form development.

This Second Edition has been completely updated with new chapters added to cover the changes in the subject matter.

It contains a very good balance between the theoretical considerations and practical aspects of parenteral dosage form development. Inclusion of topics such as freeze drying, clean-in-place steam-in-place, designing of biopharmaceutical facilities, and ophthalmic formulations in this edition strengthens the basic structure of this book and provides the reader with an excellent overview of parenteral dosage form development

The book is very well written for scientists and engineers in the pharmaceutical industry and academia.

Contents

1. The Processing of Small Volume Parenterals and Related Sterile Products
2. Factors Involved in Manufacturing Large Volume Parenterals
3. Freeze Drying: Principles and Practice
4. Design Considerations for a Parenteral Production Facility
5. Biopharmaceutical Manufacturing Facility Design
6. Personnel: The Key Factor in Clean Room Operations
7. Environmental Control in Parenteral Drug Manufacturing
8. Industrial Sterilization: A Review of Current Principles and Practices
9. Development of Ophthalmic Formulations

Index

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