- Išsiųsime per 10–14 d.d.
/https://libri-media.knygos-static.lt/57394deb-d2ee-43fd-8b33-2a51959826be/2)
- Leidėjas: Wiley-VCH GmbH
- Metai: 2025
- ISBN-10: 3527348905
- ISBN-13: 9783527348909
- Formatas: 17.4 x 24.4 x 3.2 cm, kieti viršeliai
- Kalba: Anglų
- Extra -15 % nuolaida šiai knygai su kodu: ENG15
Method Validation in Pharmaceutical Analysis (el. knyga) (skaityta knyga) | knygos.lt
Atsiliepimai
Aprašymas
Adopting a practical approach, the authors provide a detailed interpretation of the existing regulations (GMP, ICH), while also discussing the appropriate calculations, parameters and tests. The book thus allows readers to validate the analysis of pharmaceutical compounds while complying with both the regulations as well as the industry demands for robustness and cost effectiveness.
Following an introduction to the basic parameters and tests in pharmaceutical validation, including specificity, linearity, range, precision, accuracy, detection and quantitation limits, the text focuses on a life-cycle approach to validation and the integration of validation into the whole analytical quality assurance system. The whole is rounded off with a look at future trends.
With its first-hand knowledge of the industry as well as regulating bodies, this is an invaluable reference for analytical chemists, the pharmaceutical industry, pharmaceutists, QA officers, and public authorities.
EXTRA 15 % nuolaida su kodu: ENG15
Akcija baigiasi už 3d.09:18:54
Nuolaidos kodas galioja perkant nuo 10 €. Nuolaidos nesumuojamos.
- Leidėjas: Wiley-VCH GmbH
- Metai: 2025
- ISBN-10: 3527348905
- ISBN-13: 9783527348909
- Formatas: 17.4 x 24.4 x 3.2 cm, kieti viršeliai
- Kalba: Anglų Anglų
Adopting a practical approach, the authors provide a detailed interpretation of the existing regulations (GMP, ICH), while also discussing the appropriate calculations, parameters and tests. The book thus allows readers to validate the analysis of pharmaceutical compounds while complying with both the regulations as well as the industry demands for robustness and cost effectiveness.
Following an introduction to the basic parameters and tests in pharmaceutical validation, including specificity, linearity, range, precision, accuracy, detection and quantitation limits, the text focuses on a life-cycle approach to validation and the integration of validation into the whole analytical quality assurance system. The whole is rounded off with a look at future trends.
With its first-hand knowledge of the industry as well as regulating bodies, this is an invaluable reference for analytical chemists, the pharmaceutical industry, pharmaceutists, QA officers, and public authorities.
Atsiliepimai