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In’Tech Medical created a Global Regulatory Affairs Department to support medical device companies across its facilities.
“In the past 20 years, In’Tech has constantly innovated in response to market conditions and customer needs,” said Laurent Pruvost, President & CEO of In’Tech Medical. “This global regulatory initiative we are launching continues in that tradition, supporting each of our facilities in the USA, France and Malaysia, while focusing on providing customers with all the tools and data to support their product launch.”
Tania Shammo will lead the initiative as Global Regulatory Affairs & Quality Assurance Director. Her RA/QA experience spans over two decades at positions in the U.S. and internationally, with organizations such as Bradshaw Medical and Leader Biomedical.
“Tania possesses deep regulatory expertise and has a proven track-record at managing quality assurance and regulatory affairs programs internationally,” said Xavier Leroy, In’Tech’s Chief Operating Officer. “In addition to helping the In’Tech Group build rock-solid quality and regulatory foundations, I am confident that her department will also become a key ingredient to many of our customers’ regulatory strategy as they expand.”
