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Developing and Validating an HPLC Method
Developing and Validating an HPLC Method February 20, 2019 A host of resources must be harnessed to bring a drug… Read more
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Understanding the importance of stress degradation studies
Understanding the Importance of Stress Degradation Studies December 4, 2018 “Frequently time is of the essence. It is necessary to… Read more
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Mass Balance – What, When, How?
Mass Balance – What, When, How? July 10, 2018 This “fishbone diagram”, shown by permission from Steven Baertschi (S. W.… Read more
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Method Development and Validation – Are We Doing It Right?
Method Development and Validation – Are We Doing It Right? April 21, 2015 Last year, a group of academic chromatographers… Read more
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Looking at Impurity Isolation Early Can Benefit Your Drug Development Process
Looking at Impurity Isolation Early Can Benefit Your Drug Development Process July 18, 2014 Jeffrey Kiplinger, President and Founder of… Read more
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Targeted Isolation of Impurities in Pharmaceutical Compounds using SFC
Targeted Isolation of Impurities in Pharmaceutical Compounds using SFC August 30, 2013 We presented two* posters at CoSMoS 2013, Targeted Isolation™ of… Read more
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Benefits of Early Impurity Analysis to Pharmaceutical R&D
Benefits of Early Impurity Analysis to Pharmaceutical R&D August 27, 2013 We presented two/ posters at the CoSMoS 2013 (Conference… Read more
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Averica Wins Silver at 2013 CoSMoS Olympics for Chemistry Method Development
Averica Wins Silver at 2013 CoSMoS Olympics for Chemistry Development August 14, 2013 Our chemistry method development (in collaboration with Novatia,… Read more
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Using Chiral SFC/MS to Solve a Bioanalysis Problem
Using Chiral SFC/MS to Solve a Bioanalysis Problem November 29, 2012 We were asked recently to participate in a technology… Read more
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Chiral Biotransformation Analysis in Rat Plasma by SFC
Chiral Biotransformation Analysis in Rat Plasma by SFC August 31, 2012 A compound developed in a pharmaceutical lead optimization project… Read more