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We offer the expertise required to meet your regulatory challenges. Our professional staffs give guidance about what is needed to succeed for a medical device in Industry. To know more about our works call us 919-313-3960.
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ROLES THAT OFFERD BY REGULATORY AFFAIRS
1. Express critical business functions and improve productivity. 2. Tracks and manages all steps of regulatory need and life cycle.
3. Makes the complete report about global compliance by product type. 4. Handles health authorities as well as resulting commitments and tasks.
5. Organize medical products approvals and regulatory notifications. 6. supervise the product safety update reports.
7. Managing the processes around the maintenance of marketing applications. 8. Address the internal issues and to seek to minimise the negative impact.
PRESENTED BY We are specifically designed for regulated businesses and makes your FDA compliance, business process management and business communication easy.
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