Who we can help
If you are a quality manager in the pharma industry and you’re
Frustrated by constantly being on the edge of non-conformity observations!
The clock is ticking, and your remediation to-do list keeps growing!
Tired of guessing and staying in the gray zone and wish to have an immediate clear idea of your systems 21CFR Part11 and Data integrity compliance!
Desperately need to address DI and CSV issues, but it seems impossible to get the ball rolling!
What you will acheive
We have a unique methodology to put an end to your above problems
Following our unique methodology called DI+ Fast Track CSV, you will
Have a crystal-clear Idea about your Data Integrity and 21CFR Part 11 compliance state and a well-defined risk-based map on how to close the gaps!
Release your computerized systems for production 30% to 50% faster.
Achieve conformity without sacrificing the performance!
Be recognized as an effective quality leader, stand out to leadership, so people follow rules and regulations by culture.
To know more or take an action, book a free consultation call
How we can help
Lean validation strategy with best in class experts
Using a lean validation strategy and bridged business knowledge transfer, with optimized configuration efforts and accelerated documentation, makes it possible to efficiently address the data integrity requirements and validate your computer systems up to 40% faster.
DI+ Fast Track is our unique validation approach that can make this happen
Why to choose APS
DI+ Fast track CSV
We only do what we do the best
Industry recognized CSV experts, with proven records
Deep expertise of laboratory computerized systems like, LIMS, Empower, Open Lab, Chromelon, LabX, UV WinLab ... and pharmaceutical processes
Do not start from scratch
Cost efficiency and full compliance using proven approach
Shorter project length with no cutting corners and full compliance