Add to Calendar >2018-08-22 09:00:002018-08-23 17:00:00Europe/BrusselsTraining Program on Impurity ProfilingA hands-on training program for increased confidence in impurity identification, detection, and quantification in APIs and formulated drug products for pharma researchCentre of Excellence, Gurgaon
9:00 AM – 5:00 PM
To ensure patient safety, regulatory agencies have put in place guidelines which mandate the identification and profiling of impurities in APIs and formulated drug products and sets thresholds at which these impurities must be reported.
A fast, high throughput, robust, and reproducible analytical technology and method (e.g., LC-MS) is critical for increased confidence in impurity identification, detection, and quantification in pharma research. This critical information speeds drug candidate development from IND-enabling studies to NDA.
Impurity Profiling Workshop will cover:
Potential of IDA workflows for identification of impurities in QTRAP
Identification of impurities by matching mol file with MS/MS data
UV-PDA data processing
Quantitation of genotoxic impurities
The training program will take place at our Centre of Excellence situated in Gurgaon on 22-23 August 2018.
Be sure to secure your space by registering for the training today.
Please note: Only 15 spaces are available. Book now to avoid disappointment.
Participants will receive certificates after completing the training.
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