Quality is critical. Whether a Class I, II, or III Medical device, processes are in place to meet quality requirements and minimize risk.
We take pride in our strong commitment to quality.
MedPlast develops custom validation and quality control plans with customers to meet specific requirements and ensure compliance with FDA and ISO regulations. Documentation of IQ, OQ, PQ and FAI is a formalized part of launching products and can be viewed online via MedPlast Central®.
A single global quality management system is in place and reviewed continuously for effectiveness, including:
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