You are just one step away from turning your dream project to reality. We are here with our expertise to consult you on every single requirement to be fulfilled for establishing your facility. We offer you the right direction to succeed in this competitive world with our support and guidance. From selecting the right design to regulating every operation, our talented team ensures precision in every single process. In case of new facility setup, we follow all the guidelines and regulations according to Health Canada that gives our clients the confidence to rule the industry.
If you are looking for quality new facility setup then GxP Cellators is a leading cGMP Cleanroom facility advisor who supports facility designing, qualification, validation, environmental monitoring, technology transfer and routine operations.
New laboratory designing and setup
We support clients in setting up the new GLP laboratories as per Health Canada and USFDA standards. We help in laboratory design, instrument selection, instrument qualification, computer system validation, and method validation as per 21 CFR Part 58, 21 CFR Part 210/211, and ISO 17025/13485 standards.
The transition of the existing non-GLP Laboratory to GLP compliant laboratory
We also support our clients in transitioning the non-GLP laboratory to GLP compliant laboratory with FDA (21 CFR Part 58 & 21 CFR Part 210 & 211), EU, and ISO standards (ISO 17025 & 13485).