Engineering and commissioning services ensure Good Engineering Practice (GEP) for biopharmaceutical and medical device companies building new plants, expanding or repurposing existing facilities, and commissioning / decommissioning equipment.
We commission virtually any biopharma, life sciences, or medical device manufacturing equipment and utilities required for greenfield or brownfield developments, including mechanical/HVAC, hold tanks, bioreactors, harvest systems, purification systems, architectural finishes, electrical components, lighting, plumbing, purified water, waste management, telecommunications, mixed gas systems, and much more.
We work with your engineering team to review designs and verify alignment as part of the integrated commissioning, qualification, and validation (CQV) process, increasing efficiencies, reducing cost, and ensuring cGMP compliance.