Certifications & Compliance
Quality Documentation
You Can Rely On.
International trade requires meticulous documentation. We understand the requirements and work to support buyers with professional quality documentation and compliance processes.
Important Notice
Certification and documentation requirements vary according to product, origin, destination country, intended use, regulatory classification and buyer requirements. The certifications and documentation listed below are placeholders and should only be presented as “Verified” when actual documentation has been confirmed. Do not assume any certification is held unless explicitly verified.
Our Certifications
Documentation & Certifications
Below are certifications and documentation types relevant to our trading categories. Status is indicated for each.
IEC
Importer-Exporter Code
Import Export Code issued by the Directorate General of Foreign Trade (DGFT), Government of India.
Add verification status when confirmed.
APEDA
Agricultural and Processed Food Products Export Development Authority
Registration for export of agricultural and processed food products from India.
Add verification status when confirmed.
FSSAI
Food Safety and Standards Authority of India
Food safety license/registration for food products.
Add verification status when confirmed.
Spices Board
Spices Board of India
Registration with the Spices Board for export of spices from India.
Add verification status when confirmed.
CDSCO
Central Drugs Standard Control Organisation
Applicable regulatory documentation for pharmaceutical exports.
Add verification status when confirmed.
WHO-GMP
WHO Good Manufacturing Practice
GMP documentation from manufacturers, where applicable.
Applicable to manufacturer facilities. Add when verified.
ISO 13485
ISO 13485 - Medical Devices Quality Management
Quality management system certification for medical devices.
Applicable to manufacturer facilities. Add when verified.
CE Mark
CE Marking (Conformité Européenne)
CE marking documentation for applicable medical devices.
Applicable to specific products. Add when verified.
Phytosanitary
Phytosanitary Certificate
Plant health certificate for agricultural exports, issued by authorized agencies.
Issued per shipment as required by destination country.
Certificate of Origin
Certificate of Origin
Documentation certifying the country of origin of exported goods.
Issued per shipment as required.
COA
Certificate of Analysis
Laboratory analysis documentation for product quality verification.
Available per product/batch as applicable.
ISO 9001
ISO 9001 - Quality Management System
Quality management system certification.
Add when verified.
Product-Specific Requirements
Compliance by Category
Each product category has specific documentation and compliance requirements. Below is the documentation structure we support.
Spices & Agro Products
Origin
Country and region of origin documentation
Variety & Grade
Product variety, grade and quality specification
Quality Testing
Moisture, purity and quality laboratory reports
Phytosanitary
Plant health certificates as required by destination
Health Certificates
Health certificates where required by destination
Certificate of Origin
Documentation certifying country of origin
Packaging & Labeling
Compliance with destination-country requirements
Requirements vary by destination market and product classification. Documentation availability depends on manufacturer and product.
Medical Disposables
Product Specification
Detailed technical and material specifications
Sterility Status
Sterilization method and documentation
ISO 13485
Quality management certification (manufacturer)
CE Documentation
CE marking and Declaration of Conformity
Certificate of Analysis
Product quality analysis documentation
Manufacturer Details
Licensed manufacturer information
Regulatory Status
Destination-country regulatory compliance
Requirements vary by destination market and product classification. Documentation availability depends on manufacturer and product.
Pharmaceuticals
Manufacturer License
Licensed manufacturer documentation
Registration Status
Product registration in destination country
GMP Documentation
WHO-GMP or equivalent documentation
Certificate of Analysis
Batch-specific quality analysis
CPP
Certificate of Pharmaceutical Product (where applicable)
Free Sale Certificate
Free sale documentation where applicable
Batch Information
Batch/lot number, manufacturing and expiry dates
Requirements vary by destination market and product classification. Documentation availability depends on manufacturer and product.
Understanding Documentation Categories
Available Documentation
Documentation that RAGMO GLOBAL or its suppliers can provide for applicable products and shipments.
Required Documentation
Documentation typically required by destination countries or regulatory bodies for import clearance.
Country-Specific Requirements
Additional documentation that may be required by specific destination countries. Requirements should be confirmed before shipment.
Questions?
Need Compliance Information?
Our team can provide specific documentation and compliance information based on your product requirements and destination market.