نتایج جستجو برای: international harmonization

تعداد نتایج: 311925  

2015
Ravi N. Tiwari Nishit Shah Vikas Bhalani Anand Mahajan

In the present study, comprehensive stress testing of amlodipine (AM) was carried out according to International Conference on Harmonization (ICH) Q1A(R2) guideline. AM was subjected to acidic, neutral and alkaline hydrolysis, oxidation, photolysis and thermal stress conditions. The drug showed instability in acidic and alkaline conditions, while it remained stable to neutral, oxidative, light ...

2011
Sharad Pawar

This study describes the development and validation of stability indicating RP-HPLC method for Mirtazapine, an antidepressant drug. In order to investigate the stability of drug, a stress testing of drug sample by exposing it to variety of forced degradation conditions has been recommended. Mirtazapine was subjected to stress degradation 1 under different conditions recommended by International...

Journal: :Drug discoveries & therapeutics 2009
W Jirawattanapong E Saifah C Patarapanich

A simple, selective and precise stabilityindicating HPLC method for determination of glabridin diacetate and dihexanoate prodrugs was developed, validated and applied to the enzymatic and chemical hydrolysis studies. The chromatographic separation was achieved on a reverse phase C18 (Thermo Hypersil-Keystone, 250 × 4.6 mm, 5 micron) column using the mixture of acetonitrile and water as mobile p...

2014
Darlene Dixon Roger Alison Ute Bach Karyn Colman George L. Foley Johannes H. Harleman Richard Haworth Ronald Herbert Anke Heuser Gerald Long Michael Mirsky Karen Regan Eric Van Esch F. Russell Westwood Justin Vidal Midori Yoshida

The INHAND (International Harmonization of Nomenclature and Diagnostic Criteria for Lesions in Rats and Mice) Project (www.toxpath.org/inhand.asp) is a joint initiative of the Societies of Toxicological Pathology from Europe (ESTP), Great Britain (BSTP), Japan (JSTP) and North America (STP) to develop an internationally accepted nomenclature for proliferative and nonproliferative lesions in lab...

2016
Thomas Nolte Patricia Brander-Weber Charles Dangler Ulrich Deschl Michael R. Elwell Peter Greaves Richard Hailey Michael W. Leach Arun R. Pandiri Arlin Rogers Cynthia C. Shackelford Andrew Spencer Takuji Tanaka Jerrold M. Ward

The INHAND (International Harmonization of Nomenclature and Diagnostic Criteria for Lesions in Rats and Mice) project is a joint initiative of the Societies of Toxicologic Pathology from Europe (ESTP), Great Britain (BSTP), Japan (JSTP), and North America (STP) to develop an internationally accepted nomenclature and diagnostic criteria for nonproliferative and proliferative lesions in laborator...

Journal: :Pathobiology : journal of immunopathology, molecular and cellular biology 2014
Ma'n H Zawati Bartha Knoppers Adrian Thorogood

Population-based biobanks promise to be important resources for genetic research. However, the study of normal genomic variation across populations requires the collection of data and biological samples from individuals on a large scale. While international collaboration has become both a scientific and an ethical imperative, international sharing of data and samples poses many challenges. Sign...

2001
Alea M. Fairchild Bruno de Vuyst

E-Commerce can be streamlined if products and services are unambiguously identified with industryagreed XML tags through the coding of products and services according to standard classification conventions, such as the Universal Standards Products and Services Classification (UNSPSC). Standardized coding allows for more effective electronic purchasing management by spend analysis ,and assists m...

Journal: :Environmental biosafety research 2006
Nevena Alexandrova Atanas Atanassov

The OECD Blue Book, "Recombinant DNA: Safety Considerations" was published in 1986. The developed principles and concepts on the stepwise and case-by-case approach for risk assessment in the Blue Book have been used as a foundation for building national biosafety frameworks and international instruments for the regulation of the products of modern biotechnology. Twenty years after the Blue Book...

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