Who we are
We are a team of experts with hard-to-match experience in the field of validation, compliance, and quality assurance. We provide services for companies across regulated industries with a special focus on life sciences. With over 300 completed projects for Clients from four continents, we have the expertise to safely navigate you through the validation process and ensure full compliance with regulations and industry guidelines.
Keeping the validation process under perfect control, we’ll effectively eliminate any business continuity risk for your company and allow you to ship your product as fast as possible
What we can do for you
- We provide validation and qualification services spanning software, equipment, installations, premises, processes, and more, coupled with quality systems implementation and quality consulting.
- We can take your business environment from the non-compliance or compliance-risk stage to a fully validated, audit-ready state.
- With an outstanding and highly motivated team of +50 experts, we can maximize the time- and cost-efficiency of the project, guiding you smoothly through the complex process. The result is guaranteed 100% compliance.
- Keeping the validation process under perfect control, we'll effectively eliminate any business continuity risk for your company and allow you to ship your product as fast as possible
Why should you work with us?
We have an outstanding record of handling a wide array of projects across pharmaceutical, medical devices, and other regulated industries.
We combine global experience with a nuanced approach sensitive to local contexts.
We provide all-around validation services: you can partner with just one company and get things done easier, faster, safer, and cheaper.
We have comprehensive life sciences expertise enabling us to deliver finely tailored solutions for even the most demanding validation issues.
We provide early-stage comprehensive consulting to make sure the project goes the right way and that we cover all your needs
We suggest – and readily perform – early-stage validation to save you a lot of costs and effort at a later phase of the project.
We have a get-things-done attitude: we do the job from A to Z instead of just instructing you how to do it best.
We're fully self-sufficient: we have our own measuring equipment
We guarantee 100% audit-proof compliance with our work
We always stick to selected deadlines and deliver on time.
News
ECVALIDATION at the 13th Pharmaceutical Industry World Congress in Warsaw!
The Congress of the Pharmaceutical Industry World is certainly an event not to be missed
November 24, 2022
ECVALIDATION as a sponsor of the XVIII Autumn Symposium of the Pharmaceutical and Cosmetics Industry in Gdynia 17-19 October 2022!
It seems to be a tradition that we are present at the BMP Pharmaceutical and
October 21, 2022
CSV Workshops in Poznań
The penultimate edition of this year’s CSV workshops is behind us! On Friday, we visited
October 11, 2022