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Coherent with the strategy of consolidating its presence in the global Pharmaceutical domain, Coster has announced that the American FDA has recently awarded the company with a Type III Drug Master File (n. 26960) for its MDI valves: 20DR & 20DPH.
The valves are manufactured in Coster Trento (Italy) facility in a Clean Room Environment, Class 7 at rest.
The newly-awarded DMF joins another filed with the FDA in 2008 for BOVs (Bag-On-Valves) and series 1800 actuators, currently being used in association with anti-mycotic products among other applications.
For more information please send an e-mail to pharma@coster.com.