Many years of experience and hundreds of pharmaceutical projects have shown us that early involvement of our specialists is the most important prerequisite for developing and, later on, delivering the optimal solution.
We are happy – at an early stage – to contribute with ideas, advice and expertise when you are preparing your URS. We are also pleased to enter into dialogue with your operators, maintenance personnel, QA people, project managers and other key stakeholders in your project.
We also supply validation documentation – please find more information about our validation documentation services here
Our documentation is a good starting point for your subsequent qualification and validation work which we also offer to support by preparing qualification documents and participating in validation tests.
All our solutions and documentation are according to GAMP.