PharmaTechXfer Technical Transfer (Tech Transfer) Services for Finished Dosage Products (FDP) – Jamaica
MoHW / MDR-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 Jamaican and Caribbean markets.
Since 2008, we have successfully supported 150+ FDP technology transfer projects across Caribbean, Latin America, Africa, Asia, Middle East, Europe, and regulated global markets, including projects aligned with the Ministry of Health and Wellness (MoHW), Jamaica, and the Medicines and Devices Regulatory Authority (MDR), while fully complying with WHO GMP expectations—ensuring smooth technology transfer, regulatory approval, and inspection-ready commercial manufacturing in Jamaica.
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 Jamaica, we act as a technical and regulatory bridge between:
R&D → Pilot → Commercial manufacturing
Sending site (US / EU / global originator) → Receiving site (Jamaica / Caribbean)
Product development → MoHW / MDR approval → Jamaica & regional supply
All services are delivered by experienced pharmaceutical technologists, QA professionals, and Caribbean 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 & site suitability 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 qualification
Scale-up support and process validation readiness
Quality Risk Management as per ICH Q9
📑 Regulatory-Aligned Tech Transfer (Jamaica Focus)
Tech Transfer documentation aligned with CTD Module 3 (where applicable)
Compliance with:
Ministry of Health and Wellness (MoHW), Jamaica
Medicines and Devices Regulatory Authority (MDR)
WHO GMP
Support for:
New product registrations
Manufacturing site change / site addition approvals
Post-approval variations & lifecycle management
CARICOM and regional Caribbean supply dossiers
Tech Transfer documentation for authority reviews & inspections
🛡️ Post-Transfer & Operational Support
Handling MoHW / MDR authority queries related to technology transfer
Deficiency response preparation with strong scientific justification
Change control & variation documentation
Post-approval variation support
Inspection and 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 Jamaica
Pharmaceutical manufacturers
Importers and Marketing Authorization Holders (MAHs)
Regional CMOs / CDMOs
Government and institutional supply partners
Export-oriented companies supplying Caribbean markets
Jamaica & Global Regulatory Alignment
Our Tech Transfer services are designed to meet Jamaica regulatory requirements while remaining fully aligned with international standards, including:
Ministry of Health and Wellness (MoHW), Jamaica
Medicines and Devices Regulatory Authority (MDR)
WHO GMP
ICH Guidelines (Q8, Q9, Q10)
Why Clients Serving Jamaica Choose PharmaTechXfer
✅ 150+ FDP Tech Transfer projects completed
✅ Since 2008 Caribbean & global regulatory experience
✅ MoHW/MDR & 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 & Caribbean 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 Caribbean, Latin America, Africa, Asia, Middle East, Europe, and regulated global markets, including Jamaica.