Cecile Laurencin

Cecile Laurencin is a Regulatory Affairs Specialist currently employed at TRB Chemedica International since September 2023, with previous experience at Stragen where responsibilities included eCTD publishing and maintaining registration information in Switzerland. Prior to Stragen, Cecile held roles at GSK as Quality Systems Execution Senior Manager and Quality Compliance Senior Manager, focusing on SOP implementation, data integrity, and quality reviews. At Novartis Consumer Health, responsibilities encompassed compliance management in global regulatory affairs and technical documentation preparation for registration dossiers. Cecile's career began at Galderma, managing stability samples. Education includes a two-year degree in Food Industry and a Baccalauréat Scientifique.