Pharmaceutical process validation /

Código QR

Pharmaceutical process validation /

Detalles Bibliográficos
Autor principal:	Loftus, Bernard T. (Editor )
Otros Autores:	Nash, Robert A. (Editor , Editor/a)
Formato:	Libro
Lenguaje:	English
Publicado:	New York, New York : M. Dekker, c1984.
Materias:	MEDICAMENTOS > CONTROL INDUSTRIA FARMACEUTICA

Ejemplares similares

Validation of aseptic pharmaceutical processes /
por: Carleton, Frederick J. 1925 -
Publicado: (1986)

Rules and guidance for pharmaceutical manufacturers 1993 /
Publicado: (1993)

Pharmaceutical raw materials pharmaceutical products and medicinal herbs : a survey of the Netherlands and other major markets in the European Union /
Publicado: (1994)

Quality assurance of pharmaceuticals : a compendium of guidelines and related materials
Publicado: (2004)

Quality assurance of pharmaceuticals : a compendium of guidelines and related materials
Publicado: (1999)

Japan pharmaceutical reference (JPR) : administration and products in Japan : 1991-1992
Publicado: (1991)

Process chemistry in the pharmaceutical industry /
Publicado: (1999)

Pharmaceutical pricing policies in a global market /
por: Docteur, Elizabeth
Publicado: (2008)

Pharmaceutical stress testing : predicting drug degradation /
Publicado: (2011)

The Indian pharmaceutical sector : issues and options for health sector reform /
por: Govindaraj, Ramesh 1961-
Publicado: (2002)

Target discovery and validation : methods and strategies for drug discovery /
Publicado: (2020)

Examples of the development of pharmaceutical products from medicinal plants
Publicado: (2005)

Principles of pharmaceutical marketing /
por: Smith, Mickey Charles 1946-
Publicado: (1975)

Selected issues in pharmaceuticals a Background Review For Latin America and the Caribbean
por: Marquez, Patricio
Publicado: (1991)

Marketing authorization of pharmaceutical products with special reference to multisource (generic) products : a manual for national medicines regulatory authorities (NMRAs)
Publicado: (2011)

Advanced pharmaceutics : physicochemical principles /
por: Kim, Cherng-ju, et al.
Publicado: (2004)

Specifications for the quality control of pharmaceutical preparations : International pharmacopoeia
Publicado: (1971)

Pharmaceutics of Solids and Solids Dosage Form
por: Carstensen, Jens Thuro, 1926-
Publicado: (1977)

Aseptic pharmaceutical manufacturing : technology for the 1990s /
por: Olson, Wayne P.
Publicado: (1987)

Quality assurance of pharmaceuticals : a compendium of guidelines and related materials. --
Publicado: (1999)

3D printing of pharmaceuticals /
por: Awad, Atheer
Publicado: (2018)

The validation of analytical methods for pharmaceutical analysis
por: McPolin, Oona
Publicado: (2009)

Quality assurance of pharmaceuticals : a compendium of guidelines and related materials, 2011 /
Publicado: (2011)

Quality control in the pharmaceutical industry /
por: Cooper, Murray Sam n. 1923
Publicado: (1972)

Quality assurance of pharmaceuticals : who guidelines, related guidance and GXP training modules /
Publicado: (2013)

The pharmaceutical industry in India and Hungary : policies, institutions, and technological development /
por: Felker, Greg, 1966-
Publicado: (1997)

Quality assurance of pharmaceuticals
Publicado: (2004)

Quality assurance pharmaceuticals
Publicado: (1999)

Cleaning validation manual : a comprehensive guide for the pharmaceutical and biotechnology industries /
por: Haider, Syed Imtiaz, et al.
Publicado: (2010)

Cleaning validation manual : a comprehensive guide for the pharmaceutical and biotechnology industries /
por: Haider, Syed Imtiaz, et al.
Publicado: (2010)

Basic test for pharmaceutical dosage forms /
Publicado: (1991)

Risk management and risk assessment for pharmaceutical manufacturing : a contamination control perspective /
por: Sandle, Tim
Publicado: (2013)

Theory and practice of contemporary pharmaceutics /
por: Ghosh, Tapash K.
Publicado: (2005)

Essays on the history of the pharmaceutical industry /
por: Peddlers, Pill, et al.
Publicado: (1990)

Quality assurance of pharmaceuticals a compendium of guidelines and related materials
Publicado: (2007)

Elaboración de una herramienta de verificación de requisitos para los procesos de inscripción, renovación y cambios postregistro de los medicamentos de síntesis química para uso humano según la Reglamentación Técnica Centroamericana y la legislación correspondiente de Costa Rica, Honduras, Nicaragua, Guatemala, El Salvador y Panamá para Laboratorios Stein S.A. durante el primer semestre de 2022 /
por: Ramírez Ramírez, Génesis Paola 1998-
Publicado: (2022)

Manual básico de entrenamiento para representantes profesionales /
por: Arguedas G., Jorge, et al.
Publicado: (1983)

Importancia de la aplicación de una política farmacéutica nacional con el uso de medicamentos esenciales bajo el concepto de genéricos /
por: Arévalo Mulato, Maura Verónica
Publicado: (1997)

Pharmaceutical calculations /
por: Ansel, Howard C., 1933-
Publicado: (2017)

Quality control in the pharmaceutical industry /