, submission, and monitoring of PLAIR activities, prior to new product launch Manage regulatory correspondence mainly to CDER, FDA..., User fee staff, drug listing and Board of Pharmacies for state licensing submissions. Provide regulatory guidance to R...
, and Regulatory Affairs to standardize processes and cultivate a culture of continuous improvement. Key Responsibilities...Description : The Continuous Improvement Manager is responsible for leading, developing, and executing strategies...
of medical content, including complex and sensitive information. Ensures compliance with regulatory and corporate requirements... Affairs teams), representing the Medical Information function for products with limited complexity and/or multiple indications...
of medical content, including complex and sensitive information. Ensures compliance with regulatory and corporate requirements... Affairs teams), representing the Medical Information function for products with limited complexity and/or multiple indications...
of medical content, including complex and sensitive information. Ensures compliance with regulatory and corporate requirements... Affairs teams), representing the Medical Information function for products with limited complexity and/or multiple indications...
of medical content, including complex and sensitive information. Ensures compliance with regulatory and corporate requirements... Affairs teams), representing the Medical Information function for products with limited complexity and/or multiple indications...