Medical Assembly and Packaging
GDM entered the Medical Assembly and Packaging market in 1989 and was registered by the FDA in 1992 to provide Class I and Class II medical device assembly services.
GDM is ISO 13485:2016 registered and can assist in creating compliant manufacturing processes that include inspection points, material reconciliation, and product validation.
-Class 10K Cleanroom
All materials and operations are transacted through our manufacturing software to provide comprehensive batch records and real time completion status.
Compliant assembly and packaging services