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Have confidence in your data
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BioPharm
 
Remove manual interaction risks with automation

There are many steps you can take to feel more confidence in your QC data. Training and retraining your users on the steps of your SOP is helpful, but it won’t get at the heart of some data integrity issues.

Remove the steps that might be causing you headaches by incorporating a robust automated solution that removes those risky manual steps. 

You’ll be able to sleep better knowing your lab has minimized its risks from manual steps, and you can rest assured in your electronic record being “the thing” that proves you’re compliant.

Automating Biopharma Quality Control to Reduce Costs and Improve Data Integrity

Take a look at four common quality control procedures and how automation can help improve data integrity by reducing opportunities for human error, while also saving time and reducing operating costs. 
Discover QC Automation
Achieving Compliant Batch Release
  
Common QC instrumentation compliance elements are discussed and examples of instrument best practice used for QC batch release are introduced. Discover how to optimize instruments for compliance, help reduce human error, and maintain data integrity for test results. 
Read it here
Cleanroom Routine Environmental Monitoring – FDA Guidance on 21 CFR Part 11 Data Integrity

Examine the risk of error with SOPs being implemented manually. Technology exists and is commercial available to mitigate this problem and make programs more robust, reducing the impact on data integrity and also supporting the industry's move towards environmental monitoring by production staff in the cleanroom.
Environmental Monitoring Automation

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