November 2023
From Research Laboratory to GMP-Ready Facility
Moving from research-scale operations towards GMP-controlled manufacturing requires significant changes in processes, documentation, facilities and organisational responsibilities.
A structured gap assessment can help identify areas requiring development before GMP implementation. This may include personnel training, SOP systems, equipment qualification, environmental controls, documentation and quality oversight.
i-CELLBIO works with organisations to support this transition through scientific, technical and quality consultancy.