At PROCESS.ING LifeSciences Group, each project team is staffed with experts responsible for quality assurance and documentation throughout the project and beyond.
Quality assurance starts with the (re)evaluation of the existing systems and/or validation master planning for new systems followed by the system specification and risk analysis through to the Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ). We will be pleased to advise you any time on the development of the necessary master SOPs for calibration, maintenance and repair, GMP risk analyses and routine monitoring for your specific site. Rounding off our service spectrum are periodic calibrations and clean room measurements as well as computerized systems, cleaning and methods validation services.
Download: Our validation matrix at a glance (PDF).
Hanauer Landstraße 328-330
D-60314 Frankfurt am Main
Fon: +49 (0) 69 - 710 448 7 - 0
Fax: +49 (0) 69 - 710 448 7 - 19
Email: helen.kuehn@processing-lifesciences.de