Phillips Plastics Corporation® Receives EU GMP Registration
Menomonie, Wisconsin – Phillips Plastics Corporation recently received the European Union’s Good Manufacturing Practices (EU GMP) Certification for a high volume drug product currently manufactured at its Medical Molding and Assembly facility. To achieve the certification, a superior level of performance was required in order to comply with the strict rules of Europe’s Medicine and Healthcare Products Regulatory Agency (MHRA). A very unique distinction for contract manufacturing, the EU GMP certification will allow Phillips’ combination product and drug delivery device customers to tap directly into the European pharmaceutical markets. As explained by Dave Thoreson, Plant Manager at Medical Molding and Assembly, “This EU GMP Certification, combined with our 21 CFR 820 and 21 CFR 210 and 211 registrations allow us to provide world class combination product capabilities to our customers. This new certification opens up a new realm of business possibilities for Phillips and its ability to comply with European regulations in the pharmaceutical market.”
For more information, contact:
Lori Feiten
Phone – 715.386.4320
lori.feiten@phillipsplastics.com
www.phillipsplastics.com
