Regulatory Trainings

Awareness and Implementation MDR 2017 G.S.R 78 E
Performance Evaluation IVD
Risk Analysis ISO 14971:2019
Regulatory Orientation (Medical Devices)
CE Marking: MDR 2017-745. Medical Devices
CE Marking: MDR 2017-746. IVD
Medical Device Regulatory Fundamentals/ Regulatory Orientation
Medical Device Quality Management Systems (QMS) Implementation
Medical Device Risk Management Training: ISO 14971:2019
Medical Device Regulatory Submissions
Post-Market Surveillance and Vigilance
Medical Device Labeling and Packaging Compliance
Good Manufacturing Practices (GMP) for Medical Devices
Medical Device Auditing and Inspections
EU Medical Device Regulation (MDR) Training CE Marking: MDR 2017-745. Medical Devices/ CE Marking: MDR 2017-746. IVDs
FDA Medical Device Regulations Training
Clinical Evaluation and Clinical Trials for Medical Devices
QSR 21CFR Part 820

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