Helping GMP/GLP labs meet data integrity guidelines
Email alerts
Free registration
Chat area
Certificate of attendance
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.
For more information, please contact us at [email protected]
Presented by:
Dr. Caroline Cardonnel
Caroline Cardonnel has a Ph.D. in Medicinal Chemistry and Pharmacology with over 11 years of hands-on experience with Molecular Devices instruments and software. Prior to joining Molecular Devices, Caroline did her Doctoral studies at the University of Reading in the UK, where she synthetized 32 Suramin analogues and studied their effects on the formation of the Dopamine-D2s receptor-G protein Complex.