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
- Unidade: FCF
- Subjects: FARMACOLOGIA; FÁRMACOS; CONTAMINAÇÃO DE EQUIPAMENTOS
- Language: Inglês
- Imprenta:
- Publisher: AOAC International
- Publisher place: Gaithersburg
- Date published: 2004
- Source:
- Título do periódico: Abstracts
- Conference titles: 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 ; - Development and validation of HPLC methods for quantitative determination of second generation H1 antihistamines in pharmaceuticals
- Desenvolvimento de métodos para a separação enantiomérica empregando HPLC com fase estacionária quiral
- Development and validation of a HPLC and UVDS methods for quantitative determination of sotalol in tablets
- Quantitative determination of fluvastatin and atorvastatin calcium in tablets
- UV-derivative spectrophotometric and stability indicating high performance liquid chromatographic methods for determination of simvastatin in tablets
- Simultaneous quantitative determination of five sunscreens in lotion preparation by high performance liquid chromatography
- Stability of sunscreens emulsions in different types of packaging materials
- Development and validation of a UV derivative spectrophotometric method for quantitative determination of pravastatin sodium in tablets
- Development and validation of stability indicating HPLC methods for quantitative determination of pravastatin, fluvastatin, atorvastatin and rosuvastatin in pharmaceuticals
- Development and validation of sensitive methods for determination of sibutramine hydrochloride monohydrate and direct enantiomeric separation on a protein-based chiral stationary phase
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