Navigating the pharmaceutical regulatory landscape can be complex. From dossier compilation to country-specific certificates, documentation is crucial for product registration and approval. At Vaccure Pharma, we offer full-spectrum pharma product documentation support to help you export medicines, vaccines, and nutraceuticals with confidence.

We work with pharmaceutical marketing companies, importers, and healthcare agencies around the world to ensure smooth documentation and registration—saving time, avoiding delays, and ensuring regulatory compliance.

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✅ Why Is Documentation Critical in Pharma Exports?

Whether you’re exporting to Africa, Latin America, Southeast Asia, or CIS countries, most regulatory authorities require:

  • Product registration dossiers (CTD/ACTD)
  • Certificates of Pharmaceutical Product (COPP)
  • Free Sale Certificate (FSC)
  • WHO-GMP certificate
  • Certificate of Analysis (COA)
  • Labeling, leaflets & stability studies

Without proper documentation, even the best-quality medicine can’t enter the market.

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📦 What We Provide in Pharma Documentation Support

At Vaccure Pharma, we assist clients with a comprehensive documentation package, which includes:

Regulatory Certificates

  • WHO-GMP Certificate
  • Free Sale Certificate (FSC)
  • COPP (Certificate of Pharmaceutical Product)
  • Manufacturing License
  • ISO Certification

Product-Specific Documents

  • Certificate of Analysis (COA)
  • Stability data (accelerated/real-time)
  • Product specs (API/Excipient/Finished Product)
  • Packing material details

Dossier Preparation

  • CTD / ACTD Format
  • Section-wise technical writing (Module 1 to 5)
  • Compilation of administrative data
  • Labelling, patient information leaflets, etc.

🌍 Countries We Support Documentation For

We provide pharma product documentation support tailored to:

  • Africa (e.g., Nigeria NAFDAC, Kenya PPB)
  • CIS countries (Russia, Ukraine, Belarus)
  • Latin America (Peru, Bolivia, Guatemala)
  • Southeast Asia (Vietnam, Philippines, Cambodia)
  • GCC and Middle East (UAE, Saudi FDA, Oman)

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💊 Documentation for All Product Categories

We support registration documentation for:

  • Tablets, capsules, syrups, and injectables
  • Vaccines (Typhoid, Rabies, Hepatitis B, BCG)
  • Nutraceuticals (powders, supplements, herbal formulations)
  • Veterinary products (poultry vaccines, tonics, antibiotics)

🧾 Custom Label & Packaging Compliance

Every country has specific packaging needs. We provide:

  • Multilingual labels and inserts
  • Product barcodes, QR codes, serialization
  • Export-compliant outer cartons and inner packs
  • Temperature and handling instructions

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🚀 Work with Vaccure Pharma for Reliable Pharma Product Documentation Support

At Vaccure Pharma, we understand the importance of accurate and timely documentation. Our regulatory team works closely with clients to prepare submission-ready files that meet international standards. As a regulatory-compliant medicine exporter, we make your global expansion simple and stress-free.

📧 Email: info@vaccurepharma.com
📞 Phone: +91 9925178885 / +91 2613101203
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