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Dipankar singh .

💊B Pharma graduate 2026. Drug Regulatory Affairs Specialist | CTD Dossier | eCTD | CDSCO | ICH Guidelines | Pharma Compliance

Greater Delhi Area

< 1 year of work experience

Akums Drugs& Pharmaceuticals Ltd
Aug 20255 mosDec 2025

Delhi, India

- Handled regulatory documentation for 15+ product registrations and license renewals with 100% SOP compliance - Reviewed pharmaceutical pricing against NPPA guidelines and DPCO 2013 regulations with 99% accuracy - Prepared CTD-format submissions and variation filings supporting on-time product approvals - Conducted MRP verification and pricing compliance audits to catch discrepancies before regulatory review

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Dipankar singh . on Tal

Headline

💊B Pharma graduate 2026. Drug Regulatory Affairs Specialist | CTD Dossier | eCTD | CDSCO | ICH Guidelines | Pharma Compliance

About

Regulations exist to protect patients. I chose Regulatory Affairs because I want to be the person who makes that system work. I'm a B.Pharm graduate with knowledge of Drug Regulatory Affairs, completed my internship at Akums Drugs & Pharmaceuticals, and industrial exposure at Arbro Pharmaceuticals and the Indian Pharmacopoeia Commission. At Akums, I worked hands-on with regulatory documentation, dossier components, and GMP compliance — the kind of experience most freshers only read about in textbooks. I also independently developed and evaluated a neem oil antibacterial gel as my research project — applying regulatory thinking from excipient selection to physicochemical testing. What I work with: → CTD Dossier Structure | CDSCO | ICH Guidelines → Schedule M | GMP/GLP | Pharmacovigilance basics → Regulatory Writing | Stability Studies | Drug Master Files Currently looking for entry-level Regulatory Affairs or CRO roles in Delhi-NCR where I can contribute from day one and grow fast.

Location

Greater Delhi Area

Work experience

Drug Regulatory Affairs at Akums Drugs& Pharmaceuticals Ltd, Aug 2025 - Dec 2025 · 5 mos, Delhi, India, - Handled regulatory documentation for 15+ product registrations and license renewals with 100% SOP compliance - Reviewed pharmaceutical pricing against NPPA guidelines and DPCO 2013 regulations with 99% accuracy - Prepared CTD-format submissions and variation filings supporting on-time product approvals - Conducted MRP verification and pricing compliance audits to catch discrepancies before regulatory review

Dipankar singh . - Drug Regulatory Affairs in Greater Delhi Area | Tal