How to enhance productivity with an integrated compliance-ready software platform for analyses requiring chromatographic and mass spectrometric analysis
The right CDS (Chromatography Data System) ensures data quality and manages all the necessary processes along the analytical workflow from instrument control, to raw data storage and processing, right through to generating reports of the final results, allowing pharma and biopharma companies and contract research organizations to leverage their MS systems throughout various stages of research and product development, taking advantage of compliance-readiness when needed.
In this webinar, Dr. Dan Bach Kristensen, principal scientist at Danish clinical-stage antibody oncology-focused company, Symphogen, shares examples of how to boost productivity by using the right LC-MS software to streamline analytical workflows and enable the use of MS as a routine detector.
Key learning objectives:
- How to develop platform workflows supported by the right CDS for simplified characterization and quality monitoring of complex therapeutic proteins
- How to translate biopharmaceutical characterization methods into transferable, routine, compliance-ready solutions
- How to gain understanding and alignment with the analytical data generation and handling requirements for complex monoclonal antibodies
Who should attend?
Traditional pharmaceutical and biopharmaceutical companies (although any laboratory requiring compliance-ready MS data acquisition and processing capabilities will find this informative), with the main targets being: lab managers and directors, IT managers, C-Suite, QA managers, analytical scientists in existing late-stage development, QA/QC and contract laboratories running analyses requiring chromatography data system software, with focus on transferring LC-MS methods further into development where compliance-ready streamlined software solutions are needed.