ELK RIVER, MN, June 13, 2017— Cretex Companies today announced it has acquired Quality Tech Services (QTS), a supplier of outsourced packaging services to the medical device industry.
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Compliance to the UDI regulation includes the FDA public database, GUDID. The first phase of the Global Unique Device Identification Database (GUDID): Guidance for Industry document is now available..
DuPont is in the process of validating new equipment/technology for the production of Tyvek. DuPont is working with the FDA and industry leaders to qualify the new material. During the HealthPack.
Unique Device Identification (UDI) Final Rule was announced by the FDA on September 20, 2013. The rule was published in the Code of Federal Regulations as of September 24, 2013. Implementation for.
