4EasyReg 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]4easyreg.com or through the form below.
