At the start of your project we discuss the starting points of your project and the validation master plan. Together we will determine the targets, requirements and wishes of the project. With this information we will make a plan of action, to discuss with you. If we both agree, we will make an offer with clear direction of our activities.
A new project is started, but you need all your people to run the day –to-day business. Or you are missing some roles. Improvement factory can support you to qualify and validate your project. We can control the complete V-model. Writing the validation master plan, setting up the protocols and plan and execute the protocols.
Intake
Implementation
We take care of execution and/or support in the project. We use our knowledge and experience for a successful qualification. Our focus is that all your processes, installation, equipment’s, procedures and methods meet the requirements written down in DQ, IQ, OQ and PQ protocols. To assure your company meets the requirements from FDA, GMP and GLP.