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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
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