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Analytical Testing for the Pharmaceutical GMP Laboratory

Huynh-Ba, Kim
Analytical Testing for the Pharmaceutical GMP Laboratory
Analytical Chemistry: An Introduction to the Pharmaceutical GMP Laboratory presents a thorough overview of the pharmaceutical regulations, working processes, and drug development best practices used to maintain the quality and integrity of medicines. With a focus on smaller molecular weight drug substances and products, the book provides the knowledge necessary for establishing the pharmaceutical laboratory to support Quality Systems while mai...

CHF 191.00

Handbook of Stability Testing in Pharmaceutical Development

Huynh-Ba, Kim
Handbook of Stability Testing in Pharmaceutical Development
A COMPREHENSIVE AND PRACTICAL GUIDE TO STABILITY TESTING IN PHARMACEUTICAL DEVELOPMENT Stability testing is required to demonstrate that a pharmaceutical product meets its acceptance criteria throughout its shelf life and to gain regulatory approval for commercialization. Assessing drug product stability and safety can be quite complicated, and stability profile can impact many functional areas, including analytical testing, formulation devel...

CHF 188.00

Pharmaceutical Stability Testing to Support Global Markets

Huynh-Ba, Kim
Pharmaceutical Stability Testing to Support Global Markets
The International Conference of Harmonization (ICH) has worked on har- nizing the stability regulations in the US, Europe, and Japan since the early 1990s. Even though the Stability Guidelines Q1A (R2) was issued over a decade ago, issues surrounding this arena continue to surface as the principles described in the guideline are applied to different technical concentrations. As a result, the stability community has continued to discuss concern...

CHF 188.00

Pharmaceutical Stability Testing to Support Global Markets

Huynh-Ba, Kim
Pharmaceutical Stability Testing to Support Global Markets
The International Conference of Harmonization (ICH) has worked on har- nizing the stability regulations in the US, Europe, and Japan since the early 1990s. Even though the Stability Guidelines Q1A (R2) was issued over a decade ago, issues surrounding this arena continue to surface as the principles described in the guideline are applied to different technical concentrations. As a result, the stability community has continued to discuss concern...

CHF 188.00

Handbook of Stability Testing in Pharmaceutical Development

Huynh-Ba, Kim
Handbook of Stability Testing in Pharmaceutical Development
A COMPREHENSIVE AND PRACTICAL GUIDE TO STABILITY TESTING IN PHARMACEUTICAL DEVELOPMENT Stability testing is required to demonstrate that a pharmaceutical product meets its acceptance criteria throughout its shelf life and to gain regulatory approval for commercialization. Assessing drug product stability and safety can be quite complicated, and stability profile can impact many functional areas, including analytical testing, formulation devel...

CHF 236.00