Helping GMP/GLP labs meet data integrity guidelines

Laboratories, especially those involved in drug discovery or manufacture, often need to meet extensive government guidelines for Good Laboratory/Manufacturing Practice. Failure to meet these guidelines can have severe financial and legal consequences for the organisation involved.

In this webinar, Dr Caroline Cardonnnel from Molecular Devices will outline some of the requirements of these guidelines, and how software solutions for microplate readers can be used to help you achieve full FDA 21 CFR Part 11 compliance, maintaining your data integrity whilst still benefitting from streamlined data analysis and reporting.