EUDAMED Becomes Fully Mandatory from 28 May 2026: What Medical Device & IVD Manufacturers Need to Know
Pranab Sagar
24 Jun, 2025
Pranab Sagar is a regulatory affairs expert with over 16 years of experience, specializing in Regulatory Information Management Systems (RIMS), lifecycle management, and compliance for the pharmaceutical industry. His expertise spans regulatory data management, risk analysis, and strategic planning.
At Celegence, he leads regulatory initiatives, ensuring high-quality data integrity, process optimization, and seamless collaboration with stakeholders. With a strong background in clinical research and vendor management, he plays a key role in driving compliance and operational efficiency in regulatory services.
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