SINCE 1987, ACCUREG INC. HAS SERVED
THE MEDICAL PRODUCTS INDUSTRIES WORLD-WIDE
WITH REGULATORY, COMPLIANCE AND TECHNICAL CONSULTING SERVICES, HELPING OUR CLIENTS
BRING NEW PRODUCTS TO MARKET AND ACHIEVE THEIR COMPLIANCE AND QUALITY GOALS
Our Guiding Principle: IT CAN BE DONE
While the regulations are printed in “black and white,” each client’s products, processes and culture are unique.
That’s why establishing an effective, sustainable compliance environment requires a real-world, experience-based interpretation
of the regulations in relation to that client’s needs.
The professionals at AccuReg understand this. We strive to ensure our clients are neither vulnerable to quality deficiencies,
nor burdened with restrictive or elaborate processes that aren’t going to last. We work collaboratively and creatively with each client
to achieve this balance, which we call the S4 Compliance Process (Simple, Systematic, Sustainable, and Scaleable).
Like the three sides and base of a pyramid, these principles create a foundation of strength and lasting stability for any Quality System.
We’ve used this approach time and time again, on successful projects as complex as multi-year, international Consent Decree remediations,
to straightforward goals such as implementing an electronic document system at a single-owner manufacturing location.
The process works for you because it works with you. It’s our pride and mission to help you make it happen.
That’s why we say: IT CAN BE DONE.