“Regulatory standards are precious fabrics to be tailored for each company”
(Fabio Tommasi Rosso, CEO)
Years of Excellence
For over 20 years, we have been working in the medical device sector, gaining cross-disciplinary experience that covers design activities, control and optimization of production processes, regulatory compliance, implementation of quality management systems, and the design and implementation of post-market activities such as clinical investigations and clinical follow-up studies.
Furthermore, we boast extensive experience in both process and product audit activities, and we are experienced trainers who favor a technical-practical training model, being able to present numerous cases and study examples during training activities.
Why FTR Advisor?
We have chosen to personally engage in strategic consultancy for companies, providing those fundamental consulting services that form the foundation of medical device development.
Our Corporate Vision?
To simplify the approach to medical device regulation and to foster an internal organization that reaches the same objectives, even if from different perspectives.
Our Mission?
To be reliable, without making promises that cannot be kept.
To be flexible, without imposing a single work philosophy, but seeking the most suitable one for the company's reality.
To be informed, by studying a case before taking on its assignment.
To be responsible, by considering the consequences that each strategic choice may entail.
To work with passion and enthusiasm to convey positivity and find a solution even when it seems there is none.
Are you seeking expert and reliable support for training and consultancy in the field of medical devices?
Our team of highly qualified professionals provides personalized technical-practical training services to help you excel in a complex and ever-evolving environment.