Founder & Team

Pragya Dossier-DMF Services was founded with a vision to provide comprehensive and reliable regulatory affair services, addressing the complex needs of the pharmaceutical, herbal, and food industries. Our expertise extends across various facets of regulatory services, including dossier preparation, analytical method validation, bioequivalence studies, product development reports, and more, ensuring compliance with global standards such as CTD, ACTD, and ICH guidelines.

Founder

Our founder, [Your Name], is a seasoned professional with extensive experience in regulatory affairs. With a deep understanding of the intricacies involved in dossier preparation and Drug Master File (DMF) services, [Your Name] has been instrumental in shaping Pragya Dossier-DMF Services into a trusted partner for clients worldwide. Their commitment to excellence and continuous learning drives our team to deliver top-notch services that meet the stringent requirements of global regulatory bodies.

Our Team

At Pragya Dossier-DMF Services, our team is composed of skilled professionals with a diverse background in regulatory affairs, product development, technical writing, and clinical trial reporting. Each team member brings a wealth of knowledge and experience, enabling us to provide tailored solutions that cater to the specific needs of our clients. Our collaborative approach ensures that every project is handled with the utmost care and attention to detail, resulting in high-quality submissions that facilitate smooth regulatory approval processes.

Advisory Board
Our Advisory Board is actively involved in building a stronger international level dimension - in dossier consultancy and handling export registration queries (by MOH).

Dr. RajKumar Choudhary (Mumbai)
Dr. Ajay, Ph.D (Regulatory affairs)
Mr. Sachin J., B. Pharm, M. Pharm
Dr. K. R. Choudhary, Ph.D
Dr. Nidhi Sharma, Ph.D
Ms. Jayshree, B. Pharm

Regulatory (Dossier) Team:
Mrs. Ankita B, Pharm
Dr. Siddharth Reddy Ph D
Ms. Neetu Gupta M. Pharm