The FDA employs stringent guidelines via their cGMP regulations. The Medivant Healthcare facility is the most current, full-scale facility of its kind, fully compliant with cGMP in the United States. Fully automated with a novel, single line-manufacturing set-up (featuring aqueous sterile injectable products), the Chandler facility was designed by leading architects and engineers working in the larger healthcare sphere.
The facility’s in-house lab is a state-of-the-art sterility & chemistry lab, strategically equipped to handle Multi-Stage Sterility Checks as well as In-House Bud Studies. Medivant is currently only occupying 1/3rd of its space with plans to roll out over the remaining 2/3rds over the subsequent two to three years. Growth will be swift and promising.