Paul has provided regulatory advice to Ventinova since 2010. As Regulatory Affairs Manager, he is responsible for securing market access in all target countries. With a master’s degree in electrical engineering and over 15 years in medical device development, Paul has secured market access for a number of manufacturers worldwide.
Paul: “With its lean processes and documentation structure, Ventinova is very well equipped to handle the changing regulatory environment in an efficient manner.”
No less than five abstracts were presented concerning our unique ventilation techniques FCV® and EVA® during Euroanaesthesia 2019 in Vienna. Of course we enlightened these posters at our booth. Furthermore, we discussed optimization of patient ventilation on...