Select the registration or license type relevant to your product
Not sure which license applies to your product?
Book Free Consultation →Drug & Device Licenses
💊Drug License 🏪Retail Drug License 🏭Manufacturing Drug License 📦Wholesale Drug License 🏥Medical Device Registration 📋CDSCO Registration ✨CDSCO Cosmetic Import Registration 🔬CDSCO Medical Device Import License 🧴Cosmetic Manufacturing License 🧪In Vitro Diagnostic Device Mfg. LicenseImport, Export & NOC
🔬InVitro Diagnostic Device Import License ✈️Drug Export NOC 🔄Dual-Use NOC 🧫CDSCO Test License 🏛️ADC NOC 💉CDSCO Drugs Import LicenseExpert CDSO services for Medical Device registration, Drug approvals, Cosmetic compliance, and BIS/M certification — ensuring your products reach the market faster.
End-to-end support from pre-submission strategy to post-market compliance across all regulated product categories.
Complete CDSCO registration support for all classes of medical devices including in-vitro diagnostics. We handle documentation, clinical data, and regulatory liaison.
Expert guidance through India's drug approval framework — from the Drugs & Cosmetics Act, 1940 to New Drugs & Clinical Trials Rules, 2019. We handle all licence categories.
Full compliance support for cosmetic products under the Drugs & Cosmetics Act and Cosmetics Rules, 2020 — import registration, labeling review, and Schedule S compliance.
Bureau of Indian Standards certification for medical devices and healthcare products. We manage the complete application, factory audit preparation, and ISI mark licensing.
A structured approach that minimizes delays and maximizes your approval success rate.
Review existing documentation and identify gaps against CDSCO / BIS requirements.
Compile technical files, clinical data, testing reports, and regulatory submissions.
Submit to CDSCO / BIS and manage entire communication with regulators.
Respond promptly to regulatory queries with detailed, data-backed justifications.
Obtain registration certificate and support post-market surveillance compliance.
Deep expertise across all key Indian regulatory frameworks for medical products.
National regulatory body for drugs, cosmetics, medical devices & diagnostics under MOHFW.
Comprehensive framework for classification, registration, manufacturing and import of medical devices.
Primary legislation governing the import, manufacture and distribution of drugs and cosmetics in India.
Mandatory ISI certification under IS standards for notified medical devices and products.
Client approval rates across product categories
Based on 500+ filings. 2009–2024.
A dedicated team with deep regulatory intelligence and a track record of swift approvals.
Our pre-built templates and established authority relationships significantly reduce standard approval timelines.
Ex-CDSCO officials and former pharma regulatory heads with direct experience in the Indian approval system.
All client data, formulations, and technical documents are protected under strict NDAs and secure systems.
We serve international manufacturers from USA, Europe, Japan and South Korea seeking India market entry.
Every client gets a single point of contact who tracks your application status and keeps you updated.
Ongoing pharmacovigilance, renewal tracking, adverse event reporting, and label change management.
Book a free 30-minute consultation with our regulatory experts. No obligation, just clarity on your path to approval.
Connaught Place, New Delhi — 110001, India
+91 98100 00000
info@regpathcdso.in
Mon – Sat: 9:00 AM – 6:30 PM IST