Are you ready for your compliance audit?

Regulatory inspections of pharmaceutical companies are increasing. Integrated informatics solutions allow you to provide evidence that your GMP processes are validated, that you are using appropriate resources, and that your analytical data are accurate, complete and consistent. You can be sure that you have full data integrity, processes are managed according to 21 CFR part 11 requirements, and that your audit checklist will satisfy the inspectors.  

Get audit ready and achieve full data integrity with our Integrated Informatics Solutions, including LIMS, CDS and SDMS. 

New webinars on demand

Data Integrity Issues in Regulated GxP Labs

Data integrity is not just confined to emerging markets -- it is a global issue. This Fundamentals Series presentation will provide: an introduction to data integrity; definitions of data integrity; criteria to ensure data integrity in lab records; discussion of GxP regulations and guidance for data integrity, focused on GMP; and 10 most common data integrity problems and how to resolve them.

Managing Pharmaceutical Lab Data Management to Ensure Compliance

Join Stacey Brown and William Leonard, Senior Validation Analysts for Informatics at Thermo Fisher Scientific, to understand more about the complex requirements of pharmaceutical data management: key concerns in implementation and validation; ongoing system management; how to ace your audits.

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