Optimarc is committed to the ongoing training of its ARCs. At least one annual session is organized according to their needs and regulatory developments.
- 01/2017, Clinical investigations for CE marking of medical devices and ISO 14155: 2011 norms,
- 01/2016, the new European regulation on clinical trials,
- 04/2013, Audit preparation for an investigation center,
- 06/2013, Training in Good Clinical Practice (GCP) for Investigators,
- 05/2011, Regulatory submissions of biomedical research in France / Clinical trials regulatory of medical devices.