Impurities - News

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7 Questions to Ask to Get the Most From API Manufacturing

Tags: API Manufacturing | CDMO | Cost | Development Cost | Impurities | SEQENS

Posted August 2, 2021
The Role of Stability-Indicating Methods to Determine the Potency of an API

Tags: API Manufacturing | Blog | Controlled Substance | Impurities | Stability Testing

Posted November 23, 2020
10 Strategies for Lowering Elemental Impurities in APIs

Tags: API Manufacturing | Blog | ICH | Impurities

Posted September 21, 2020
10 Steps to Control or Eliminate Genotoxic Impurities in API Manufacturing

Tags: API Manufacturing | Blog | Impurities | NEC

Posted July 6, 2020
How Well Do You Know Your CDMO’s Manufacturing Capacity?

Tags: API Manufacturing | Blog | Equipment | Impurities

Posted February 10, 2020
How to Stem the Flow of Tainted Generic Drugs and Product Recalls

Tags: API Manufacturing | Blog | FDA | Impurities

Posted July 8, 2019
Want a Strong API Launch?

Tags: Analytical Methods | API Manufacturing | Blog | Impurities

Posted December 14, 2018
How to Control Impurities during API drug manufacturing

Tags: API Manufacturing | Impurities | Video

Posted February 19, 2018
Three Ways to Save Money when Managing Impurities During API Scale-Up

Tags: Blog | Development Cost | Impurities | Scale-up

Posted December 1, 2017
Dealing with the Unexpected in API Development

Tags: Blog | FDA | Impurities | Project Management | Research and Development | Technology Transfer

Posted July 30, 2017