PharmaTechXfer Global Technical Transfer (Tech Transfer) Services for Finished Dosage Products (FDP) – Seychelles
SMRA Aligned | WHO GMP–Focused | Globally Trusted
PharmaTechXfer, a scientific arm of Zoesoe Exports Pvt. Ltd., provides end-to-end Technical Transfer (Tech Transfer) Services for Finished Dosage Products (FDP) to pharmaceutical importers, distributors, MAHs, and partner manufacturers operating in Seychelles, supporting product registration, supply continuity, and compliant sourcing from approved global manufacturing sites.
Since 2008, we have successfully delivered 150+ FDP technology transfer projects across Africa, Asia, Middle East, Europe, and Latin America, ensuring smooth scale-up, regulatory compliance, and sustainable commercial supply.
Who We Are
PharmaTechXfer is a specialized pharmaceutical technology transfer service provider, focused exclusively on Finished Dosage Form (FDP) Tech Transfer documentation, execution support, and regulatory query handling.
We support Seychelles-based organizations by bridging the gap between:
Overseas WHO GMP-approved manufacturing sites → Approved supply sources
Product development → SMRA approval → Market supply
Import-based portfolios → Alternate & backup manufacturing site qualification
All Tech Transfer activities are performed by experienced pharmaceutical technologists, QA experts, and regulatory professionals, ensuring WHO GMP–compliant and SMRA-acceptable technology transfer.
Our Core Tech Transfer Services (FDP)
🔬 Technical Transfer Documentation
Product & process knowledge transfer dossiers
Manufacturing process summaries & flow diagrams
Master Formula Records (MFR) & Batch Manufacturing Records (BMR)
Control strategy with CPP / CQA mapping
Manufacturing site & equipment equivalency justification
Packaging & labeling transfer documentation (English-compliant)
🏭 Manufacturing & Process Transfer Support
Import-to-alternate manufacturer technology transfer
Site-to-site transfer (India / EU / ROW ↔ Approved supply sites)
Process comparability & optimization support
Scale-up & validation readiness assistance
Risk assessment aligned with ICH Q9 (where applicable)
📑 Regulatory-Aligned Tech Transfer (Seychelles Focus)
Tech Transfer documentation aligned with WHO-based regulatory expectations
Compliance with Seychelles Medicines Regulatory Authority (SMRA)
Support for:
Product registration & renewals
Manufacturing site & supplier changes
Variations & post-approval lifecycle management
Supply continuity & emergency site approvals
Tech Transfer documentation for authority review & audits
🛡️ Post-Transfer & Lifecycle Support
Handling SMRA queries and deficiencies
Scientific justification & response preparation
Change control & comparability documentation
Post-approval variation support
Inspection & audit readiness assistance
Dosage Forms We Support
Tablets (IR, MR, ER, EC)
Capsules (Hard gelatin & HPMC)
Oral liquids & suspensions
Dry syrups
Powders & granules
Semi-solid dosage forms (where applicable)
Industries & Clients We Serve in Seychelles
Pharmaceutical importers & distributors
Marketing Authorization Holders (MAHs)
Hospital & institutional suppliers
Government & public health procurement agencies
NGOs & donor-supported health programs
Indian Ocean region–focused pharmaceutical companies
Regional & Global Regulatory Coverage
Our Tech Transfer services support Seychelles-based companies sourcing from:
WHO GMP-approved global manufacturing sites
Africa, Asia, Europe & Middle East supply partners
Aligned with:
WHO GMP
ICH principles (Q8, Q9, Q10 – where applicable)
SMRA regulatory requirements
International best practices for small island markets
Why PharmaTechXfer?
✅ 150+ FDP Tech Transfer projects completed
✅ Since 2008 Africa & global regulatory experience
✅ Strong understanding of small-island, import-dependent pharmaceutical markets
✅ Authority-ready, practical documentation
✅ End-to-end lifecycle & post-approval support
✅ Proven success with alternate manufacturer & supply continuity projects
Our Approach
Scientific. Practical. Regulator-Focused.
Product & process understanding
Gap analysis against SMRA / WHO GMP
Customized Tech Transfer strategy
WHO-aligned documentation & execution
Post-transfer support until stable market supply
About Zoesoe Exports Pvt. Ltd.
PharmaTechXfer operates as a scientific arm of Zoesoe Exports Pvt. Ltd., a globally trusted pharmaceutical consulting and technical services organization supporting manufacturers across Africa, emerging, semi-regulated, and regulated markets worldwide.