The Medical and Regulatory Affairs team at Meisys manages and oversees the company's core services, including drug safety, regulatory consultancy, and medical information. They ensure compliance with industry standards, provide expert medical advice on product development and marketing, support medical writing and continued medical education, and operate call centers for patient support programs. Additionally, they handle pharmacovigilance activities, ensuring the proper tracking and reporting of adverse events, and maintain systems for recording and reporting drug safety and medical information. Through their expertise, they contribute to maintaining high-quality standards and regulatory adherence for Meisys' pharmaceutical clients.