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Worried about Data INtegrity?

Looking for an efficient way to validate your computer systems?

We are specialized to help clients exactly like you.

Save you up to 40% time and effort on your projects, using our unique approach.

Book a free discovery call to learn more

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

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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

Book a free discovery call to know all details

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 

efficiently meet your conformity require
 
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Testimonials

  • Karina Comito

    Head of Quality Control

    Omega Laboratories

    We entrusted APS team with the validation of the Empower software as well as the Winlab software. The team is very competent, and their technical knowledge is really strong. I was also very satisfied with the availability, flexibility, and speed of execution. Our deadlines were very tight!
    I highly recommend you use their services.

  • Hugo Tremblay

    Project Manager

    Pharmascience

    APS is a trusted, results-oriented collaborator team .that shows great professionalism in the execution and management of project tasks. They are eager for new knowledge that clearly allows them to stand out in a corporate environment or in the provision of consulting services. APS is a strategic partner in the achievement of objectives and the success of any project

  • Amir Hossein Naderi

    Directeur du laboratoire de chimie

    CCrest Laboratories

    Excellent service à la clientele, très bon niveau d'expertise dans le diagnostique des problèmes instrumentaux, Excellent niveau de communication et pédagogie.

  • Kamel LTaief

    Team Leader Analytical Instrumentation

    Pharmascience

    Un haut niveau d’expertise au niveau de CSV, Data integrity, 21CFR Part 11 et compétences GMP. Avec son maîtrise des dernières versions des plusieurs softwares tel que Empower 3, chromeleon , LabX ... L’équipe APS a démontré beaucoup d’efficacité et intégrité dans son service à la clientèle.

 
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