Additional Regulatory Services (MSC, FSC, NCC & NPPA)
To expand your medical device business globally or participate in government tenders, secondary CDSCO certificates are essential. We facilitate the procurement of Market Standing Certificates (MSC) to prove your commercial record and Free Sale Certificates (FSC) to authorize international exports. Additionally, we coordinate compliance with the National Pharmaceutical Pricing Authority (NPPA) to prevent legal pricing penalties on notified medical devices.
Key Benefits
- Enable global export expansion in compliance with international health ministries
- Qualify for institutional tenders and government bids via certified MSC
- Avoid pricing penalties and legal queries through proactive NPPA coordination
Recognized Standards
Our Methodology
Requirement Analysis
Determine eligibility and criteria for FSC, MSC, or NPPA filings.
File Preparation
Compile historical sales data, drug/device formulations, and manufacturing logs.
Authority Liaison
Coordinate with state and central drug control offices to review and sign documents.
Delivery
Issue certified certificates to the client for export or tendering.
Required Documents
Common Questions
Related Regulatory Insights
Navigating the New CDSCO Medical Device Regulations: A Definitive Compliance Guide
Understand the regulatory shift under India's Medical Device Rules (MDR) 2017, classification pathways, and MD-15 import licensing requirements for global manufacturers.
The MD-42 Trade License: Selling Medical Devices in India
A breakdown of the MD-42 wholesale registration requirements for distributors, importers, and traders operating in India.
Need Assistance with Additional Regulatory Services (MSC, FSC, NCC & NPPA)?
Our experts are ready to guide you through every step of the regulatory process. Let's discuss your project today.
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