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.

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.

You will learn:

  • How to overcome potential data integrity problems of Windows-based file systems
  • How to achieve compliance in a single secure system
  • How to go paperless easily

 

Register to view webinar