#Industry News
Propasil in the pharmaceutical sector!
New opportunities for our dehydrators.
We are excited to announce that our 'Propasil' Tyvek desiccant pouches have been registered with the US Food and Drug Administration (FDA) under a Drug Master File (DMF) Type III.
What is a Drug Master File?
Drug Master Files are confidential documents sent to the FDA containing detailed information on facilities, materials or processes used in the manufacture, processing, storage and packaging of pharmaceutical products intended for human use.
A Type III Drug Master File, in particular, provides crucial information for evaluating the materials used in the packaging of drug products in order to identify any adverse interactions that could compromise the integrity of the drug.
