| Medisize
Press Release |  |
Medisize's Netherlands Facility Achieves FDA Registration
27/03/06, Hillegom, The Netherlands: Medisize, a specialist in custom-made, single use, sterile medical devices and primary pharmaceutical packaging, has achieved FDA registration at it's Netherlands based facility located in Hillegom.
Managing Director, Willem van den Bruinhorst, comments, "Receiving FDA registration for our Dutch plant is a key milestone for Medisize. The registration endorses our commitment to operating within the strictest quality standards. Furthermore we are better positioned to serve existing and attract new customers through offering a choice of FDA registered facilities."
About Medisize:
Medisize supplies innovative, high quality and cost effective solutions to the healthcare market and industry with the focus on Airway Management and on Development and Manufacturing of medical devices and pharmaceutical primary packaging. Medisize is ISO 13485 accredited, FDA registered and authorised for CE marking. The company has manufacturing operations in The Netherlands, Ireland, Switzerland and the Czech Republic.
Medisize is a member of the Gurit-Heberlein Group. (www.gurit.com).
To learn more about Medisize visit: www.medisize.com/dm.
Edisonstraat 1
2181 AB Hillegom
The Netherlands
Tel: +31 (0) 252 576 888
Fax: +31 (0) 252 519 825
Web: www.medisize.com/dm
Email: info@medisize.nl
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