IQ. OQ. cGMP. ASAP.Once we've designed and built your system, it makes sense to have MECO be responsible for the validation. After all, our complete understanding our your project helps ensure it will be done right the first time and in less time than a third party. IQ & OQ protocols and their execution for only a portion of a project are all too common in the industry.
Ideally, MECO begins the validation process at the start of your project with the understanding or development of the user requirements. We will carry this through to the operational qualification at our factory or on your site.
At MECO, we provide comprehensive validations services that meet or exceed industry standards. Our Installation Qualification (IQ) and Operational Qualification (OQ) protocols verify the installation and operation of the equipment both in our facility and on site. Each protocol is written in accordance with current Good Manufacturing Practices (cGMP) and is FDA-compliant.
What's unique about our validation team is its wide breadth of capabilities. Our range of services include:
As you would expect, our team has a thorough understanding of each and every MECO product. But only MECO is able to validate other manufacturers' equipment. It's a major convenience that can also yield significant time-savings.