The Medical Device Manufacturer's Calibration Compliance Checklist

For medical device manufacturers, calibration compliance goes beyond keeping instruments accurate. Your processes need to demonstrate that monitoring and measuring equipment is properly controlled, traceable and capable of producing valid results – with the records to prove it. From meeting ISO 13485:2016 requirements to dealing with out-of-tolerance equipment, there are several areas Quality Managers need to consider when preparing for an audit.

Our Medical Device Manufacturer’s Calibration Compliance Checklist brings these requirements together in one practical resource. Discover what to check across your calibration programme, what to look for in calibration certificates and which records you should have ready for a notified body, customer or internal audit. Read more and download the checklist to see how your current calibration processes measure up.