Professional Expertise in Regulatory Affairs

Charul Gaur is a Senior Regulatory Affairs Specialist with over five years of experience in the medical device and pharmaceutical sectors. With a B.Pharm degree from Dr. A. P. J. Abdul Kalam Technical University, Lucknow, she has built a strong foundation in regulatory strategy, compliance, and quality systems.

Charul’s expertise spans SaMD, CDSCO, USFDA, ISO 13485, cGMP, WHO guidelines, enabling her to navigate complex regulatory landscapes effectively.

At Corpseed, Charul has earned a reputation for delivering efficient, timely, and fully compliant regulatory solutions. She is driven by a deep commitment to client satisfaction, ensuring each project meets specific requirements and is completed on time. By tailoring solutions to the unique needs of each client, she ensures that regulatory challenges are met with seamless precision, allowing businesses to focus on their core objectives.

From Pharma to Medical Devices

Charul’s professional journey began in the pharmaceutical industry, where she honed her skills in regulatory strategy, quality systems, and compliance. Her transition into the medical device industry marked a significant step in her career, further expanding her regulatory knowledge. In this field, she became well-versed in regulatory submissions, licensing, and compliance strategies, focusing on medical device regulations and international standards. This broad expertise has helped businesses stay compliant while achieving their commercial goals.

Interests Outside Work

Beyond her professional life, Charul enjoys activities that foster creativity and balance. Calligraphy is one of her passions, reflecting her meticulous attention to detail. Yoga and gardening offer her a peaceful retreat, helping her recharge and maintain mental clarity. These interests contribute to her well-rounded personality, enhancing her ability to approach challenges with fresh perspectives.

Future Aspirations

Charul’s aspirations focus on expanding her regulatory expertise and staying ahead of global regulatory trends. She aims to simplify the compliance process, helping businesses grow and innovate while ensuring they meet all necessary regulatory standards. With her dedication to continuous learning, she strives to be a leader in regulatory affairs, providing efficient and innovative solutions to complex compliance challenges.

"Empowering medical device innovation through expert regulatory strategy and compliance."

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