Lopamudra Misra

I am a dedicated Regulatory Associate with extensive experience in the pharmaceutical industry, particularly in regulatory compliance and quality assurance. My journey began with a solid academic foundation, earning a B.Pharm and an M.Pharm, where I excelled in my studies and developed a keen interest in regulatory affairs.

In my current role at Wipro, I have honed my skills in vigilance reporting and regulatory submissions for medical devices across multiple countries. I take pride in my ability to manage complex regulatory processes, ensuring compliance with local and international standards. My proactive approach has led to exceeding complaint handling KPIs and maintaining a high level of customer satisfaction through effective communication and problem-solving.

As a Subject Matter Expert in various medical device lines, I am committed to continuous learning and improvement. I thrive in challenging environments and am eager to contribute my expertise to a dynamic team focused on innovation and excellence in the pharmaceutical sector.