VALIDATION


YOUR DAILY STRUGGLE:
  • Your IT department is struggling to provide appropriate software development life-cycle documentation.
  • Audit processes take too long due to the lack
    of electronic documentation
  • Lost opportunities with food, pharmaceutical, cosmetics, or medical device customers that require suppliers to be compliant with FDA regulations (FDA 21 CFR Part 11)

    As the FDA increases regulatory enforcement
    of 21 CFR 11, many companies will struggle with procedural controls of their computer systems.

    Without electronic systems in place that incorporate electronic signatures, appropriate access control, and provides audit logs, your customers will move their business to more reliable suppliers.
THE NULOGY DIFFERENCE:

With Nulogy, you don’t have to worry about
the heavy lifting. Our software enables easy
to demonstrate source code control, audit logs, secure access, electronically capture signatures, and more. Nulogy customers serve worldwide food, pharmaceutical, and cosmetic brands.

Our professional services team will walk you through the 10-step process to help breeze through IQ, OQ, and PQ.

LEARN WHAT OUR CUSTOMERS ARE SAYING:

“The use of Nulogy’s solutions
has enhanced our quality control systems and has helped us increase customer satisfaction. It’s enabled us to grow our company with regards to both turnover and profitability.”MICHAEL BRIGGS—PRESIDENT
MARSDEN PACKAGING

Use PackManager To Make Smart
Plans That Deliver Results

LEARN HOW →

Ensure Your Audit Processes Are Validated

CONTACT US →

Thank You for subscribing to our Website.

You've been added to our distribution list.