Process validation has many hurdles and challenges. Our experts have in-the-field expertise and can alleviate any concerns and help make your projects less daunting. We have the expertise and know-how to write your protocols as well as execute and finalize any and all reporting.
QVR can assist with validation of quality, production and R&D software applications, and computer systems to comply with 21CFR part 11.
Equipment can be as unique as the product to be manufactured. With our OJT experts, no matter how specific or tailor-made your equipment is, we can provide validation services that are both cost and time effective. We work with you and your teams to customize to the Master Validation Plan that suits your business/budget needs while maintaining the gold standard needed to meet your compliance needs.
We provide talent to supplement your team, and support your organization’s research and rescue projects.
QVR will shorten your search for top performing Life Sciences professionals and directly recruit from a pool of talent not readily available and accessible on job boards.
QVR can provide project and FSP support for your organization within quality, regulatory, and validation functions.