Webinar Date/Time: Airing 1: Thursday January 19, 2023 at 11am EST | 4pm GMT| 5pm CET Airing 2: Thursday January 19, 2023 at 2pm EST | 1pm CST| 11am PST
The ease-of-use and the chromatography-based automated AssayMAP Bravo protien sample prep system can now be used in labs that require compliance regulator standard such as 21 CFR Part 11. The addition of compliance enabling features to the AssayMAP Bravo allows seamless transfer between labs so the system to be used across the biotherapeutic development process.
The AssayMAP Bravo is a flexible yet easy-to-use automated micro chromatography-based protein sample preparation platform that leverages packed resin-bed cartridges, precision-flow control, and preoptimized applications to perform a wide variety of sample preparation workflows required during biotherapeutic development. We have made several advances that allow the AssayMAP Bravo to address even more of the drug development process. The system can now use large capacity cartridges, work in 21 CFR part 11 compliant labs, and automatically generate reports detailing the sample preparation steps executed. These new capabilities enable walkup operation, simplified documentation, and seamless method transfer between labs, so projects can be moved forward as quickly as possible.
Key Learning Objectives:
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Steve Murphy, Ph.D.
Workflows and Applications
Steve Murphy earned his Ph.D. at the University of California, San Francisco and did post-doctoral work at Stanford University. For several years, Steve worked at multiple biotechnology companies developing and manufacturing high throughput drug discovery assays. For the last 12 years, Steve has been leading the development of automated protein sample prep workflows for protein quantitation and characterization on the AssayMAP Bravo platform.