Pre-Validated Medical Packaging Solution

This approach helps OEMs improve the process of getting a product into a validated sterile barrier system. Due to the complex requirements of the medical device industry, the internal resources of device OEMs are drawn primarily to the device R&D and regulatory arenas. However, once the device R&D is complete, there is still a major hurdle left to tackle: how to get a product into a validated sterile barrier system.

Posted in: Bio-Medical, Manufacturing & Prototyping, Custom & Contract Manufacturing, Packaging, FDA Compliance/Regulatory Affairs, Medical, Briefs, MDB


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