Cleaning process validation of pharmaceutical formulation production areas containing drugs with potent pharmacological activity (2004)
- Authors:
- USP affiliated authors: SINGH, ANIL KUMAR - FCF ; KEDOR, ERIKA ROSA MARIA - FCF ; SANTORO, MARIA INES ROCHA MIRITELLO - FCF
- Unidades: FCF; FCF; FCF
- Subjects: FARMACOLOGIA; FÁRMACOS; CONTAMINAÇÃO DE EQUIPAMENTOS
- Language: Inglês
- Imprenta:
- Publisher: AOAC International
- Place of publication: Gaithersburg
- Date published: 2004
- Source:
- Título do periódico: Abstracts
- Conference title: AOAC International Annual Meeting and Exposition
-
ABNT
FÁZIO, Tatiana T. de; SINGH, Anil Kumar; KEDOR-HACKMANN, Erika Rosa Maria; SANTORO, Maria Inês Rocha Miritello. Cleaning process validation of pharmaceutical formulation production areas containing drugs with potent pharmacological activity. Anais.. Gaithersburg: AOAC International, 2004. -
APA
Fázio, T. T. de, Singh, A. K., Kedor-Hackmann, E. R. M., & Santoro, M. I. R. M. (2004). Cleaning process validation of pharmaceutical formulation production areas containing drugs with potent pharmacological activity. In Abstracts. Gaithersburg: AOAC International. -
NLM
Fázio TT de, Singh AK, Kedor-Hackmann ERM, Santoro MIRM. Cleaning process validation of pharmaceutical formulation production areas containing drugs with potent pharmacological activity. Abstracts. 2004 ; -
Vancouver
Fázio TT de, Singh AK, Kedor-Hackmann ERM, Santoro MIRM. Cleaning process validation of pharmaceutical formulation production areas containing drugs with potent pharmacological activity. Abstracts. 2004 ; - Validation of analytical methods and stability studies of quinolonic antibiotics in pharmaceutical preparations
- Validation of a high performance liquid chromatographic method for sunscreen determination in emulsions
- The effect of packaging materials on the stability of sunscreen emulsions
- Desenvolvimento de métodos para a separação enantiomérica empregando HPLC com fase estacionária quiral
- Determinação de isoflavonas por cromatografia líquida de alta eficiência em formulações farmacêuticas
- Normal phase and reverse phase liquid chromatographic methods for enantiomeric separation of few NSAIDs on S, S-Whelk-O 1'trade mark' column
- Validation of a novel and efficient analytical method for the quantitative determination of pancuronium bromide in injections by high-performance liquid chromatography
- Development and validation of a HPLC and a UV derivative spectrophotometric methods for determination of hydroquinone in gel and cream preparations
- Quantitative determination of ciprofloxacin and norfloxacin in pharmaceutical preparations by high performance liquid chromatography
- Desenvolvimento e validação de um método por cromatografia líquida de alta eficiência para a determinação simultânea de filtros solares
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