.Represent company interests with local government agencies, industry associations and/or other organizations to negotiate legislation and regulations .Maintain awareness of the regional regulatory requirements so as to assess the impact and implementation of required company compliance with all regulations, laws and policies that affect the current company products/projects and provide regulatory support in-house on any medical affairs initiatives .Monitor and interpret local regulatory issues and trends that will impact the clinical development environment of clinical trials, product registration/variations/renewals of medicinal products, medical devices and/or biologics and initiate timely sharing with operational and business development teams .Develop and maintain a database of regional regulatory requirements