Regulatory Affairs Team

The Regulatory Affairs Team at Cromos Pharma is responsible for ensuring that clinical trials comply with all regulatory requirements, both locally and internationally. They manage the submission and maintenance of regulatory documents, liaise with regulatory authorities such as the FDA and EMA, and provide strategic guidance to ensure successful approval and conduct of clinical studies. This team plays a critical role in navigating the complex regulatory landscape to facilitate accelerated study start-up timelines and maintain the highest quality of clinical data.