QualityMedDev provides trainings focused on the following topics:

ISO 13485:2016 and 21 CFR 820 Quality Management System

EU Medical Device Regulation 2017/745

MDSAP – Medical Device Single Audit Program

Internal Auditor according to ISO 13485

Risk Management, ISO 14971 and ISO /TR 24971

Post-Market Surveillance according to EU MDR and IVDR

Software Verification and Validation (IEC 62304, PEMS Validation).

Trainings are available online or on-site and an official certificate of completion will be delivered to all the participants.

Final examination to be used as method for training effectiveness can be performed upon specific request.

For any information please contact us at info[at]qualitymeddev.com or through the form below.

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