Molecular Devices

eBook: Path to compliance in GMP/GLP labs

GMP or GLP labs using microplate readers in their workflows need to verify that the microplate readers function within manufacturing specifications and that the analysis software complies with regulations for electronic record keeping (21 CFR Part 11) as defined by the FDA.

Our SoftMax® Pro GxP Compliance Software includes the tools needed to achieve 21 CFR Part 11 compliance. In addition, our compliance tools and services cover the installation qualification (IQ) and operational qualification (OQ) workflow.

To download the eBook, please fill out the form below.

By submitting your details, you confirm that you have reviewed and agree with the Molecular Devices Privacy Policy, and that you understand your privacy choices as they pertain to your personal data as provided in the Privacy Policy under “Your Privacy Choices”.