My career path has allowed me to explore different visions of the medical device field: the vision of the industry, mainly as Regulatory Affairs Manager, and then that of the notified body as Technical Documentation Evaluator.
These different experiences have forged in me a conviction: medical devices represent an essential contribution to therapeutic strategies and to the functioning of health care institutions.
The diversity, complexity and technological performance of medical devices make it exciting to think about their development and marketing strategies.
Thus, I seized the opportunity to confront myself with these enriching issues by becoming a regulatory consultant at nexialist.