Compile the Regulatory documents for the related stakeholders and as per local regulations. Review local artworks and materials as needed in local language. Support in the notification process with local authorities for medical devices as applicable. Review local regulatory related procedures in markets as needed and gather the information from the team to propose the final comments. Supporting the assessment of documentation to meet in-country local requirements. Supporting in compiling local in-country documentation and /or follow-up with in-country regulatory and legal manufacturers /business units regulatory team. Support in building databases with completion and review.