PharmaTechXfer Technical Transfer (Tech Transfer) Services for Finished Dosage Products (FDP) – Fiji
MoHMS / FDA Fiji–Compliant | WHO GMP Aligned | 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 manufacturers, Marketing Authorization Holders (MAHs), and regional partners supplying or manufacturing for the Fijian market.
Since 2008, we have successfully supported 150+ FDP technology transfer projects across Oceania, Asia-Pacific, Asia, Middle East, Africa, Europe, and Latin America, including projects aligned with the Ministry of Health and Medical Services (MoHMS), Fiji, and FDA Fiji regulatory expectations, while fully complying with WHO GMP standards—ensuring smooth technology transfer, regulatory approval, and reliable medicine supply in Fiji.
Who We Are
PharmaTechXfer is a specialized pharmaceutical technology transfer consulting partner, focused exclusively on Finished Dosage Product (FDP) Tech Transfer documentation, execution support, and regulatory query handling.
For companies manufacturing in or supplying to Fiji, we act as a technical and regulatory bridge between:
R&D → Pilot → Commercial manufacturing
Sending site (regional / global) → Receiving site (Fiji / Pacific region)
Product development → MoHMS / FDA Fiji approval → National & Pacific Island supply
All services are delivered by experienced pharmaceutical technologists, QA professionals, and regulatory experts, ensuring GMP-compliant, authority-acceptable, and inspection-ready technology transfer.
Our Core Tech Transfer Services (FDP)
🔬 Technical Transfer Documentation
Product & process knowledge transfer dossiers
Manufacturing process descriptions & flow diagrams
Master Formula Records (MFR) & Batch Manufacturing Records (BMR)
Critical Process Parameters (CPP) & Critical Quality Attributes (CQA) mapping
Equipment equivalency & scale-up justification
Packaging & labeling technology transfer documentation (English compliance)
🏭 Manufacturing & Process Transfer Support
R&D to commercial scale technology transfer
Originator-to-local / site-to-site technology transfer
Equipment mapping, process optimization & line suitability
Scale-up and process validation readiness
Quality Risk Management as per ICH Q9
📑 Regulatory-Aligned Tech Transfer (Fiji Focus)
Tech Transfer documentation aligned with CTD / eCTD Module 3
Compliance with:
Ministry of Health and Medical Services (MoHMS), Fiji
FDA Fiji
WHO GMP
Support for:
New product registrations
Manufacturing site change / site addition approvals
Post-approval variations & lifecycle management
Public-sector, donor-funded & regional Pacific supply dossiers
Tech Transfer documentation for authority reviews & GMP inspections
🛡️ Post-Transfer & Operational Support
Handling MoHMS / FDA Fiji authority queries related to technology transfer
Deficiency response preparation with strong scientific justification
Change control & variation documentation
Post-approval variation support
Inspection 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 Fiji
Pharmaceutical manufacturers
Importers and Marketing Authorization Holders (MAHs)
Regional CMOs and partner manufacturing sites
Government, NGO & donor-funded health programs
Export-oriented companies supplying Pacific Island nations
Fiji & Global Regulatory Alignment
Our Tech Transfer services are designed to meet Fiji regulatory requirements while remaining fully aligned with international standards, including:
Ministry of Health and Medical Services (MoHMS), Fiji
FDA Fiji
WHO GMP
ICH Guidelines (Q8, Q9, Q10)
Why Clients Serving Fiji Choose PharmaTechXfer
✅ 150+ FDP Tech Transfer projects completed
✅ Since 2008 Asia-Pacific & global regulatory experience
✅ MoHMS/FDA Fiji & WHO GMP-aligned documentation
✅ End-to-end tech transfer lifecycle support
✅ Strong authority query & deficiency handling
✅ Proven, inspection-friendly approach
Our Approach
Scientific. Structured. Regulator-Focused.
Product & process understanding
Gap analysis between sending & receiving site
Customized Tech Transfer & Pacific-region strategy
GMP & authority-aligned documentation
Post-transfer support until process stabilization
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 Asia-Pacific, Asia, Africa, Middle East, Europe, and regulated global markets, including Fiji.