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Hi My Name Satish Mehra I noticed your medical devices and thought I’d reach out. I work with foreign manufacturers entering the Indian market, handling CDSCO approvals (MD-42 & MD-41), Sugam portal filings, and query resolution. If you’re a Manufacturer or Distributer out of India ,exploring India registration or import licensing, I’d be happy to share a quick overview or compliance roadmap. If you need any help or service pls feel free call or whatsapp me. 📲 WhatsApp: +91 8920964801 Best regards, Satish Mehra

Medical Device Testing Licence in India – CDSCO Approval via SUGAM Portal Now Essential for U.S. Companies Entering Billion Market

Medical Device Testing Licence in India – CDSCO Approval via SUGAM Portal Now Essential for U.S. Companies Entering $15 Billion Market

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A Medical Device Testing Licence in India is a regulatory permit granted by the Central Drugs Standard Control Organization (CDSCO) via the SUGAM portal for importing or manufacturing small quantities of medical devices. This license is essential for testing, evaluation, clinical investigation, demonstration, and performance studies before full commercial approval. For U.S. medical device makers […]

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Role of Authorized Indian Agent in MD-14 License India process 2026

Role of Authorized Indian Agent in MD-14 License India process 2026

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Role of Authorized Indian Agent in MD-14 License India process – Imagine this, A top-tier overseas producer has cutting-edge stents or diagnostic kits that can be shipped to India. The Device meet each worldwide standard. But shipments pile up at customs, delayed for months—or worse, rejected outright. The explanation? An Approved Indian Agent filed no

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Step-by-Step Guide to Medical Device Registration India for US Manufacturers 2026

Step-by-Step Guide to Medical Device Registration India for US Manufacturers 2026

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Medical Device Registration – Securing CDSCO Approval via MD-14 Import LicenseUS medical device manufacturers face a high-potential yet complex opportunity in India, one of the world’s fastest-growing healthcare markets. With rising demand for advanced diagnostics, implants, surgical tools, and digital health solutions, India’s medical device sector is expanding rapidly. However, compliance with the Central Drugs

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CDSCO import license fees and timeline for Class C medical devices India

CDSCO import license fees and timeline for Class C medical devices India

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CDSCO import license fees and timeline 2026 – Importing Class C medical device into India? These moderate-to-high danger merchandise—like ventilators, blood luggage, or certain diagnostic imaging gear—require a compulsory import license from the Central Medicine Standard Management Group (CDSCO). The method runs by means of Kind MD-14 (utility), resulting in Kind MD-15 (license), submitted by your Indian Approved Agent by way of the SUGAM portal. Charges and timelines have not been modified considerably because of the Medical Units Guidelines, 2017 (MDR 2017). As of 2026, the construction stays in US {dollars} (or equal INR

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Documents required for CDSCO MD-14 application foreign manufacturers

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Documents required for CDSCO MD-14 Software | What Overseas Producers Want in 2026 Importing medical units into India? For those who are overseas producers, you won’t be able to apply immediately. The method begins with Kind MD-14, submitted by your appointed Indian Licensed Agent (IAA) via the CDSCO’s SUGAM portal. Approval results in the import license in Kind MD-15. This requirement stems from the Medical Gadgets Guidelines, 2017 (MDR 2017). As of 2026, the principles stay constant—no main modifications reported for import licensing. The appliance calls for a mixture of authorized, regulatory, quality,

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How to apply for MD-14 import license for medical devices in India 2026

How to apply for MD-14 import license for medical devices in India 2026

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MD-14 Import License for Medical Devices in India: The No-BS Guide That Gets Your Shipments Moving Ever watched a container of critical ventilators or stents sit idle at Mumbai port for weeks because one form didn’t line up? Here’s the truth: without the right MD-14 import license from India’s CDSCO, your medical devices don’t clear

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MD-14 License India: Step By Step CDSCO Import License for Foreign Medical Device Manufacturers

MD-14 License India: Step By Step CDSCO Import License for Foreign Medical Device Manufacturers

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Introduction: MD-14 License India MD-14 License India – India represents one of the most compelling growth stories in global healthcare. With a population exceeding 1.4 billion and rising healthcare expenditure, the Indian medical devices market is projected to expand from approximately US$14–19 billion in 2025 to US$50 billion by 2030, at a CAGR of 15–26%.

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VSD Best Regulatory Affairs Services in Delhi 2026

VSD Best Regulatory Affairs Services in Delhi 2026

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if you’re in pharma, medical devices, biologics, cosmetics or food, and you want faster CDSCO approvals, licenses, or full regulatory compliance in India… Delhi is the strategic hub where opportunities come together. Because Delhi is the Regulatory Capital of India, hosting the CDSCO headquarters at the FDA Bhawan, it offers faster approvals and direct access

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What exactly is a TAC Certificate? What is TAC Approval in India | how do you actually get it?

What exactly is a TAC Certificate? What is TAC Approval in India | how do you actually get it?

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If you’re exporting cars, two-wheelers, three-wheelers, EVs, or automotive components into India, this is non-negotiable. Let’s break it down clearly, step by step, like we always do. What is TAC Approval / TAC Certificate? TAC stands for Type Approval Certificate (sometimes called CMVR Type Approval). It’s an official certification issued by the Indian government proving

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