Consultancy Services relating to design, validation and Qualification of Clean Rooms within Gene Therapy Innovation and Manufacturing Centre

Services are required for a number of tasks during the Qualification and Validation stages of the build completion of the Research and Development facilities including all Quality Control, Clean Room areas in grades C and grade D environments in addition to all process areas across the site and supporting site operations such as major infrastructure and support services such as logistics in addition to other areas. These works are to cover the following areas / requirements:- Qualification Requirement Matrix prepar...