Pharmaceutical Data Management Information
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 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.
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.
It’s calm in the office of this Global LIMS Manager at a top 10 international biopharmaceutical company. Everything appears to be running smoothly. But how much work is going on under the surface?
Find out what you need to know about FDA inspection audits and data integrity.
Read our new brochure that details how you can get your lab 'audit-ready' with Thermo Scientific Integrated Informatics.
Discover the latest integrated informatics solutions for the Pharmaceutical Industry in this tablet friendly eBook that includes informative videos, case studies and applications.