End-to-end Pharma Sourcing Services, project management, supplier sourcing, factory audits, quality assurance & documentation (CTD/eCTD), and compliant shipping & logistics.
Global Pharma Sourcing & Export
Expert Support Across Every Step of Pharma Sourcing and Export.
At CI Pharma, our Global Services provide complete support for sourcing and exporting pharmaceutical products worldwide.
Services
Our experienced team provides end-to-end solutions.
Project Management
Full-cycle coordination from initial inquiry to final delivery.
Quality Assurance
Detailed documentation, regulatory compliance, and product safety checks.
Factory Audit
On-ground inspections and third-party audits to verify manufacturing standards.
Sourcing
Identifying and vetting the best suppliers based on your product and regional needs.
India Business Services
We help global businesses in India with local representation, coordination, and communication.
Shipping & Logistics
Secure packaging, customs handling, and reliable global delivery.
Our Global Pharma Services are designed for businesses that demand efficiency, compliance, and trust. Whether you need a single shipment or a long-term sourcing partner, CI Pharma ensures smooth operations across all stages of international trade.
Industry Sectors We Serve
Pharmaceuticals (Finished Dosage Forms)
Comprehensive sourcing for tablets, capsules, injectables, and more—meeting strict GMP and global compliance standards.
APIs & Bulk Drugs
High-quality active pharmaceutical ingredients and bulk drugs from certified manufacturers worldwide. We follow WHO GMP guidelines to ensure regulatory compliance.
Nutraceuticals
Sourcing nutraceutical supplements tailored to your market’s regulatory and quality requirements.
Herbal & Ayurvedic Products
Export-ready herbal and ayurvedic products backed by traditional expertise and modern compliance.
Medical Devices & Diagnostics
Certified medical devices and diagnostic solutions for hospitals, clinics, and global healthcare providers.
Services FAQs
Answers to common questions about our Services including audits, QA, documentation, and logistics.
We qualify manufacturers against GMP, verify certifications, conduct audits, and maintain supplier scorecards. Each shipment is backed by COA, stability (where applicable), and batch records.
Yes. We prepare/validate CTD/eCTD dossiers, DMF coordination, and labeling/artwork per market needs. For US market guidance, see the US FDA drug manufacturing resources.
Quotes in ~24–72 hours for standard SKUs. Lead times vary by product and market; we coordinate production, QC release, export paperwork, and customs to meet agreed timelines.
Finished dosage forms, APIs & bulk drugs, nutraceuticals, herbal/ayurvedic products, and selected medical devices & diagnostics—each with market-specific compliance support.
Product name, dosage/strength, pack format, quantity, target country, and required certifications (e.g., WHO GMP, EU-GMP, USFDA). We’ll align suppliers and timelines accordingly.