Tutorials & Videos

How a complete set of software and validation tools for microplate readers can help GMP/GLP labs meet FDA data integrity guidelines

Laboratories operating under GMP or GLP regulations must follow guidelines set by agencies to protect scientific integrity or demonstrate quality assurance of manufactured products. Regulated labs using microplate readers in their workflows need to verify that they are functioning within manufacturing specifications and that the data acquisition and analysis software complies with regulations for electronic record keeping. In this webinar, learn how SoftMax Pro 7.1 GxP Software is Molecular Devices and its customers’ reply to the new FDA guidelines about data integrity which were released in April 2016.

How a complete set of software and validation tools