In global pharmaceutical trade, a single missing or incorrect document can delay shipments or result in product rejection. At Medivaara, our documentation experts ensure every export meets the regulatory, legal, and quality requirements of the importing country.
We understand:
Import/export regulations by country
Pharma compliance standards (WHO, EU, USFDA)
Timelines and legal procedures
Comprehensive Documentation for Every Export
Document Checklist :
Proforma & Commercial Invoices
WHO-GMP Certificates
MSDS (Material Safety Data Sheet)
Certificate of Analysis (COA)
Packing List
Air Waybill (AWB)
Import/Export Licenses
Free Sale Certificate (if applicable)
Country-specific Health Authority Documents
We Understand the Rules — So You Don’t Have To
From US FDA regulations to Africa’s NAFDAC or Middle East customs declarations, we tailor every documentation package to match the legal and pharmaceutical norms of your destination country.
If you’re a healthcare provider, government buyer, or distributor looking to access trusted cancer medicines, we’re here to support you. Partner with Medivaara and help save lives — one shipment at a time.