Purpose of Document
According to ISO 19011:2018, an audit is a systematic, independent, and documented process that evaluates whether a medical devices company complies with regulatory prerequisites and good practices (GxPs).
These audits are conducted for the initial inspection/qualification or ongoing supplier management to ensure that the suppliers meet your company’s requirements and industry regulations and standards applicable to the manufacture and quality of your company’s medical devices. They can focus on the supplier/vendor itself or its outsourced suppliers (if separate from the supplier).
This procedure defines the processes for conducting external audits to ensure that your company is selecting a service/product supplier that meets your requirements and subsequent requirements of regulators, Notified Bodies, or other certification bodies to ensure compliance to ISO 13485 (7.4.1), 21 CFR (820.50) and MDR (2017/745) and IVDR (2017/746).