Artixio

Author name: Disha Chatterjee

Disha Chatterjee contributes valuable insights into global regulatory frameworks, with hands-on experience in product approvals, market access, renewals, and variations. Her background includes working on drug product formulation and addressing regulatory deficiencies. With a strong grasp of submission requirements and authority expectations across multiple regions, Disha brings clarity and precision to regulatory processes. She is a regulatory affairs expert with a keen focus on aligning documentation with regional standards. Her articles offer clear, experience-backed perspectives on successful submission strategies.