Sales Director Europe, BioResearch Molecular Devices
Laboratories operating under GMP or GLP regulations must follow strict guidelines set by agencies such as the FDA 21 CFR Part 11 and EudraLex Annex 11 to protect scientific integrity and demonstrate quality assurance of manufactured products. Regulated labs using microplate readers in their workflows must verify that the data acquisition and analysis software complies with regulations to pass audits successfully. In this tutorial, we will highlight the features of Molecular Devices GxP Software to enable researchers to meet data integrity requirements and work with confidence in a validated environment. Join us and learn more!
