CfPA-The Center for Professional Advancement, Amsterdam, The Netherlands
2-3 May 2018
Who Should Attend?
This course is designed to provide training to biopharmaceutical personnel on the analytical regulations and method validation. Regulations and how they pertain to analytics, method qualification and validation, method transfers and method trending are all major course topics. Personnel with experience or just getting starting will both benefit from this course. This course is recommended for Quality Control, Quality Assurance, Analytical Scientist, Research Associates, Product Development, Manufacturing, Validation, though any inquiring minds within this industry are welcome to join. Course Description
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Invited Speakers:
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 Rachel Monsef, Consultant to the pharmaceutical and biopharmaceutical industries |
Rachel Monsef is a consultant to the biopharmaceutical industry for analytical and quality control. She has 17 years’ experience working with many types of assay for all stages of drug development. She has been responsible for method development, method qualification, method validations, assay transfer, characterization work, and stability studies. She has also worked with manufacturing groups to develop and perform assays to support their efforts. She has previously worked for Seattle Genetics and Alder Biopharmaceuticals and is currently consulting for Alder Biopharmaceuticals.
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Maximize Your Learning!
Attend this course and its Companion Course:
Biopharmaceutical Analytics: Regulations and Validations
30 April-1 May 2018 • Amsterdam • Course ID #2779