Sökt på: Sökresultat
totalt 8 träffar
How to Build and Maintain an Effective Pharmaceutical Quality Management System
How to Build and Maintain an Effective Pharmaceutical Quality Management System shares unique insights on how to improve our understanding of human factors in pharmaceutical …
Principles of Parenteral Solution Validation
Principles of Parenteral Solution Validation: A Practical Lifecycle Approach covers all aspects involved in the development and process validation of a parenteral product. By using …
How to Scale-Up a Wet Granulation End Point Scientifically
How to Scale-Up a Wet Granulation End Point Scientifically provides a single-source devoted to all relevant information on the scale-up of a wet granulation end point. Contents …
How to Integrate Quality by Efficient Design (QbED) in Product Development
The development of a robust drug product requires juggling many competing priorities such as overcoming scientific challenges, following regulatory requirements, and managing …
How to Design and Implement Powder-to-Tablet Continuous Manufacturing Systems
How to Design and Implement Powder-to-Tablet Continuous Manufacturing Systems provides a comprehensive overview on the considerations necessary for the design of continuous …
How to Develop Robust Solid Oral Dosage Forms
How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval uses a practical and hands-on approach to cover the development process of solid oral dosage forms in …
How to Validate a Pharmaceutical Process
How to Validate a Pharmaceutical Process provides a “how to? approach to developing and implementing a sustainable pharmaceutical process validation program. The latest volume in …
How to Optimize Fluid Bed Processing Technology
How to Optimize Fluid Bed Processing Technology: Part of the Expertise in Pharmaceutical Process Technology Series addresses the important components of fluid bed granulation, …