PharmaTechXfer Technical Transfer (Tech Transfer) Services for Finished Dosage Products (FDP) – Vietnam
DAV-Compliant | ASEAN, WHO & ICH 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 serving the Vietnamese market.
Since 2008, we have successfully supported 150+ FDP technology transfer projects across Asia, Middle East, Africa, Europe, and Latin America, including projects aligned with Drug Administration of Vietnam (DAV), Ministry of Health, and WHO GMP expectations—ensuring smooth technology transfer, regulatory acceptance, and sustainable commercial manufacturing.
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 Vietnam, we act as a technical and regulatory bridge between:
R&D → Pilot → Commercial manufacturing
Sending site (ASEAN / overseas) → Receiving site (Vietnam)
Product development → DAV approval → Domestic & export supply
All services are delivered by experienced pharmaceutical technologists, QA professionals, and regulatory experts, ensuring GMP-compliant, DAV-acceptable, and inspection-ready technology transfer.
Our Core Tech Transfer Services (FDP)
🔬 Technical Transfer Documentation
Product & process knowledge transfer dossiers
Detailed 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
🏭 Manufacturing & Process Transfer Support
R&D to commercial scale technology transfer
Site-to-site technology transfer (ASEAN & global sites)
Equipment mapping, line suitability & process optimization
Scale-up support and process validation readiness
Quality Risk Management as per ICH Q9
📑 Regulatory-Aligned Tech Transfer (Vietnam Focus)
Tech Transfer documentation aligned with CTD / eCTD Module 3
Compliance with DAV (Vietnam MoH), ASEAN CTD, and WHO GMP requirements
Support for:
New product registration dossiers
Manufacturing site change / site addition approvals
Post-approval variations & lifecycle management
Export-oriented dossiers (ASEAN, GCC, Africa, LATAM, ROW)
Tech Transfer documentation for DAV inspections & GMP audits
🛡️ Post-Transfer & Operational Support
Handling DAV / MoH 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 Vietnam
Pharmaceutical manufacturers
Marketing Authorization Holders (MAHs)
Contract Manufacturing Organizations (CMOs / CDMOs)
Local and multinational brand owners
Export-oriented pharmaceutical companies
Vietnam & Global Regulatory Alignment
Our Tech Transfer services are designed to meet Vietnam DAV requirements while remaining fully aligned with international regulatory standards, including:
Drug Administration of Vietnam (DAV)
ASEAN GMP / ACTD
WHO GMP
ICH Guidelines (Q8, Q9, Q10)
Why Clients Serving Vietnam Choose PharmaTechXfer
✅ 150+ FDP Tech Transfer projects completed
✅ Since 2008 ASEAN & global regulatory experience
✅ DAV & WHO 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.
Comprehensive product & process understanding
Gap analysis between sending & receiving site
Customized Tech Transfer & regulatory strategy
GMP & DAV-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 ASEAN, South Asia, Middle East, Africa, and regulated global markets, including Vietnam