COURSE ID 2780

BioPharmaceutical Analytics: Regulations and Validations

AVAILABLE On-demand
6 Hours

On-Demand

Offering Price
$ 855
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Team Training

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Individual courses are remarkably effective. But sometimes when you have a specific need, it helps to have expert guidance right in the room with you and your team.

In that case, we’re happy to design a custom training for your entire team, whether online—or on-site.

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Remember – at checkout you can choose to take this course On-demand. We offer a 10% group discount when you register 2 of more attendees (up to 10). Contact us for larger groups.

This 6 hour accredited ON DEMAND training will teach basic analytical regulations as they apply to method validations. This course, divided into four segments, will go through multiple bioanalytical methods and how to examine them for validation readiness and how to perform a validation. The methods in this course will include UV-VIS, SE-HPLC, HIC HPLC, Affinity HPLC, SDS-PAGE, IEF Gels, CE-SDS, cIEE and ELISA.

This ON DEMAND course is designed to provide training to biopharmaceutical personnel on the analytical regulations involving method validations. Regulations and how they pertain to analytics, method qualification and validation and method trending will all be course topics. Personnel with experience or just getting started will both benefit from this course.

This course is recommended for:

– Quality Control

– Quality Assurance

– Analytical Scientist

– Research Associates

– Manufacturing departments

course instructor

Rachel Monsef
Consultant to the biopharmaceutical and pharmaceutical industries

Rachel Monsef’s Courses
Rachel Monsef is a consultant to the biopharmaceutical and pharmaceutical industry for analytical and quality control. She has 19 years experience working with many types of assays for all stages of drug development. Ms. Monsef has been responsible for method development, method qualification, method validation, assay transfers, characterization work and stability studies. She has been involved in method trouble shooting and assisting with troubled validations. Ms. Monsef has worked extensively with coordinating method development and validation work performed at CMOs as well as trouble shooting methods that do not have the robustness needed for regulatory compliance. She previously worked at Alder (now Lundbeck) and Seattle Genetics and is consulting for both companies.