About
Currently working as a Regulatory Affairs Trainee at IPCA Laboratories Ltd. in the ROW Regulatory Affairs department, where I manage regulatory activities for CIS markets (Russia and Uzbekistan), including preparation and submission of query responses for ophthalmic products, tablets, and nutraceuticals. I am also responsible for regulatory support for medical devices marketed across LATAM, Africa (East & West), and Asian markets, handling registration documentation, lifecycle management, and country-specific regulatory compliance while coordinating with cross-functional teams to ensure timely submissions and approvals.
Skills & Expertise
No skills added yet.
Research Interests
Regulatory Affairs
Drug Regulatory Affairs
Regulatory Compliance
Regulatory frameworks
Ensuring Product compliance with regulatory bodies
Connect With Me
Education
sanjivani collage of pharmaceutical education and research
Jamia Hamdard University (JMU)
SAVITRIBAI PHULE PUNE UNIVERSITY
Projects
Preparation and compilation of dossier of opthalmic drug product for Latam and CIS markets
Publications (3)
The control of biofilm-related infection on biomedical devices continues to pose a significant clinical challenge due to microorganism biofilm structural resilience and its tolerance to antimicrobials...
A fundamental requirement for generic parenteral drug products is ensuring patient safety and therapeutic equivalence to reference products. Injectable formulations bypass physiological barriers such...
Artificial intelligence (AI) and robotics are reshaping modern healthcare by enhancing diagnostic accuracy, streamlining clinical workflows, and improving patient outcomes. AI supports early disease d...
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