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Category Archives: method development

APIs & Chemistry: The Importance of Understanding Critical Reaction Parameters

Posted on October 6, 2014 by

Active Pharmaceutical Ingredients (APIs, or – in layman’s terms – the ingredients that makes drugs work) have grown increasingly complex. Today’s equivalent of boiling tree bark into a tincture typically…

Posted in analytical science, Capabilities, Chemistry, critical reaction parameters, drugs, genotoxic impurities, method development, QA/QC, R&D, scale-up | Comments Off on APIs & Chemistry: The Importance of Understanding Critical Reaction Parameters

Analytical Capabilities and Drug Quality – Key to Successful Pharma Outsourcing

Posted on September 23, 2014 by

Last week, we wrote a post on new analytical methods for the detection of impurities that our R&D group had developed for the drug Febuxostat. And we’ve done the same…

Posted in analytical science, APIs, Capabilities, Chemistry, Contract Manufacturing, CRO/CMO, Febuxostat, genotoxic impurities, method development, Neuland Labs, QA/QC, regulatory | Comments Off on Analytical Capabilities and Drug Quality – Key to Successful Pharma Outsourcing

Investigation of Various Impurities in Febuxostat

Posted on September 8, 2014 by

In this month’s issue of PharmTech, team members at Neuland’s R&D Center in Hyderabad published a peer-reviewed article on the analysis and management of impurities in the drug Febuxostat. Febuxostat, a…

Posted in analytical science, Capabilities, Chemistry, drugs, Febuxostat, method development, Neuland Labs, peer-review, Pharm Tech, Pharmaceutical Technology, QA/QC, regulatory | Comments Off on Investigation of Various Impurities in Febuxostat