How To Reduce Data Integrity Risk
Data integrity problems continue to plague the pharmaceutical industry – especially in regulated laboratories – with violations still being identified by health authority inspectors over 18 years after the Able Laboratories fraud case.
The aim of this guide is to provide practical advice on how to reduce data integrity risk and ensure GxP compliance. Learn from those in the industry who have failed to comply with data integrity regulations and who have been on the receiving end of an FDA inspection.
Download this guide to discover ways to prevent data integrity issues from arising, including:
- Improving manual colony counting practices
- Implementing informatics solutions to automate and enforce working practices
- Utilizing instrument logbooks effectively