PharmaTechXfer Technical Transfer (Tech Transfer) Services for Finished Dosage Products (FDP) – Mauritius
PBRB-Compliant | WHO & PIC/S 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, MAHs, and regional partners supplying the Mauritian market.
Since 2008, we have successfully supported 150+ FDP technology transfer projects across Africa, Asia, Middle East, Europe, and Latin America, including projects aligned with Pharmacy Board of Mauritius (PBRB) requirements and WHO / PIC/S GMP expectations—ensuring smooth technology transfer, regulatory acceptance, and sustainable pharmaceutical supply in Mauritius.
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 Mauritius, we act as a technical and regulatory bridge between:
R&D → Pilot → Commercial manufacturing
Sending site (EU / overseas) → Receiving site (Mauritius)
Product development → PBRB approval → Local & export supply
All services are delivered by experienced pharmaceutical technologists, QA professionals, and regulatory experts, ensuring GMP-compliant, PBRB-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/French alignment where required)
🏭 Manufacturing & Process Transfer Support
R&D to commercial scale technology transfer
Site-to-site / originator-to-local 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 (Mauritius Focus)
Tech Transfer documentation aligned with CTD / eCTD Module 3
Compliance with PBRB Mauritius, WHO GMP, and PIC/S GMP expectations
Support for:
New product registrations
Manufacturing site change / site addition approvals
Post-approval variations & lifecycle management
Export-oriented dossiers (Africa, SADC, ROW)
Tech Transfer documentation for PBRB inspections & GMP audits
🛡️ Post-Transfer & Operational Support
Handling PBRB authority queries related to technology transfer
Deficiency response preparation with strong scientific justification
Change control documentation
Post-approval variation support
Pre-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 Mauritius
Pharmaceutical manufacturers
Contract Manufacturing Organizations (CMOs / CDMOs)
Marketing Authorization Holders (MAHs)
Multinational companies using Mauritius as a regional export hub
Export-oriented pharmaceutical companies supplying Africa & ROW markets
Mauritius & Global Regulatory Alignment
Our Tech Transfer services are designed to meet Mauritius PBRB requirements while remaining fully aligned with international regulatory standards, including:
Pharmacy Board of Mauritius (PBRB)
WHO GMP
PIC/S GMP
ICH Guidelines (Q8, Q9, Q10)
Why Clients Serving Mauritius Choose PharmaTechXfer
✅ 150+ FDP Tech Transfer projects completed
✅ Since 2008 Africa & global regulatory experience
✅ PBRB & WHO/PIC/S GMP-aligned documentation
✅ End-to-end tech transfer lifecycle support
✅ Strong regulatory 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 & export-oriented strategy
GMP & PBRB-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 Africa, Asia, Middle East, Europe, and regulated global markets, including Mauritius