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Export Documentation

Complete documentation.
Every shipment covered.

Every Ramso export shipment comes with a full regulatory documentation package — prepared, verified, and ready for your country's import clearance process.

📋
Certificate of Analysis (CoA)
Batch-specific quality test report confirming the product meets pharmacopoeial specifications. Issued for every shipment.
🏅
WHO-GMP Certificate
Our manufacturing facility certification confirming compliance with World Health Organisation Good Manufacturing Practices.
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CDSCO Drug Licence
Central Drugs Standard Control Organisation licence (Form 28) confirming legal manufacture under Drugs & Cosmetics Act, 1940.
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Certificate of Origin
Issued by the Indian Chamber of Commerce confirming the product is manufactured in India.
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Packing List
Detailed list of all items in the shipment including quantities, batch numbers, and pack sizes.
🧾
Commercial Invoice
Export invoice with HS codes, unit pricing, total value, and Incoterm.
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Stability Data (ICH Zone IVb)
Accelerated and real-time stability data at 40°C/75% RH — required for tropical market registrations.
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SmPC / Product Dossier
Summary of Product Characteristics and full regulatory dossier for product registration in your country.
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Country Product Permit (CPP)
Free Sale Certificate and Country of Origin confirmation for importing country regulatory submission.
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Master Formula Record (MFR)
Complete manufacturing process documentation for regulatory review.

Request your documentation package

Tell us your target market and we will prepare the complete documentation package required for your country's import and registration process.

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