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Volumn 93, Issue 4, 2010, Pages 1228-1235

Development and validation of a micellar high-performance liquid chromatographic method for determination of risedronate in raw material and in a pharmaceutical formulation: Application to stability studies

Author keywords

[No Author keywords available]

Indexed keywords

CHROMATOGRAPHIC ANALYSIS; DEGRADATION; DRUG PRODUCTS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; ORTHOPHOSPHORIC ACID; PARTICLE SIZE; PARTICLE SIZE ANALYSIS; SULFUR COMPOUNDS;

EID: 77956167672     PISSN: 10603271     EISSN: None     Source Type: Journal    
DOI: 10.1093/jaoac/93.4.1228     Document Type: Article
Times cited : (13)

References (24)
  • 23
    • 77956148278 scopus 로고
    • ICH Harmonized Tripartite Guideline, Current Step 4 Version, Parent Guidelines Dated 27 October, Complementary Guidelines on Methodology Dated 6 November 1996, Incorporated in November 2005, accessed February 15, 2008, International Conference on Harmonization, Geneva, Switzerland
    • ICH Harmonized Tripartite Guideline, Validation of Analytical Procedures: Text and Methodology, Q2 (R1), Current Step 4 Version, Parent Guidelines Dated 27 October 1994, Complementary Guidelines on Methodology Dated 6 November 1996, Incorporated in November 2005, http://www.ich.org/LOB/media/MEDIA417.pdf, accessed February 15, 2008, International Conference on Harmonization, Geneva, Switzerland
    • (1994) Validation of Analytical Procedures: Text and Methodology, Q2 (R1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.