Adiuvo expertise in quality system development, SOP writing, FMEA, and Six Sigma will help bring your firm into compliance with applicable regulations and standards, identify and resolve problem areas in your current quality system, all with a practical approach to quality management. At Adiuvo we have developed, implemented, and had to adhere to various quality systems throughout our careers. We understand the need for the system to not only meet regulations and standards, but also the importance of maintaining it a system that is not over cumbersome for the user.
At Adiuvo we will not only assist you in identifying potential problems and roots causes, we will also work with you to create solutions to those problems. Your problem is our problem, and there is no problem too big or too small for Adiuvo to tackle with your firm. With our experience, we have seen a lot over the past 30 years, and together we can identify the most effective resolutions.
In the manufacturing world today, we all need to cut costs. Where your staff has
been redirected to the issues within your firm, utilize Adiuvo to perform your Supplier
audits or work with your Supplier to resolve quality issues that may be recurring
or effecting your manufacturing environment negatively.
When you have a quality issue with a large customer that cannot seem to be resolved, let Adiuvo provide an objective view to the issue to bring resolution to the issue at hand.
If you do not have time to perform your internal audits, or quality issues have caused you to question your current systems, Adiuvo can provide an objective view to your auditing program, or perform an independent audit of your facilities, and working with your team, identify solutions.
Lisa Foster, Adiuvo Principal, is a leader in the sterilization industry and leads the AAMI and ISO working groups to develop the standards for the industry. In her 25 years in the sterilization industry, she has seen it all when it comes to sterilization.
Her extensive experience in developing sterilization processes, validations, quality system requirements and knowledge of standards relating to sterilization has helped numerous manufacturers throughout her tenure. She will focus on the defining the root cause, identifying corrective action, and assist you in developing the plan to implement the corrective action all the way to your sterilization provider.