[NEW] Webinar Spotlight
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.
New SoftMax® Pro 7.1 GxP Software addresses the FDA guidelines on data integrity by storing files in a Microsoft SQL database, establishing a complete system audit trail which records all document and data modifications.
Join our webinar and learn how to:
- Overcome potential data integrity problems of Windows-based file systems
- Achieve compliance in a single secure system
- Go paperless easily
Date: May 15, 2019
Time: 7:00AM PDT, 10:00AM EDT, 3:00PM BST, 4:00PM CET