Shivamogga, Karnataka, India
• M.Pharm student specializing in Regulatory Affairs with a strong interest in pharmaceutical regulations, compliance, and global healthcare standards. • Currently working on a thesis project focused on Electronic Medical Device Adverse Event Reporting for Medical Devices in US . • Familiar with ICH guidelines, CTD/eCTD structure, and regulatory frameworks including USFDA, EMA, and CDSCO. • Developing knowledge in regulatory documentation, scientific writing, literature review, and submission processes. • Detail-oriented, quick learner, and passionate about building a career in Regulatory Affairs and the pharmaceutical industry. • Open to opportunities in Regulatory Affairs and related domains.
Training in Production,QC & Packaging department