PharmaTechXfer Technical Transfer (Tech Transfer) Services for Finished Dosage Products (FDP) – Lebanon

MoH-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 serving the Lebanese 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 Lebanon Ministry of Public Health (MoPH) requirements and WHO / PIC/S GMP expectations, ensuring smooth technology transfer, regulatory acceptance, and sustainable commercial supply.

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 Lebanon, we act as a technical and regulatory bridge between:

  • R&D → Pilot → Commercial manufacturing

  • Sending site (originator / overseas) → Receiving site (Lebanon or regional)

  • Product development → MoPH approval → National & export supply

All services are delivered by experienced pharmaceutical technologists, QA professionals, and regulatory experts, ensuring GMP-compliant, MoPH-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

🏭 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 (Lebanon Focus)

  • Tech Transfer documentation aligned with CTD / eCTD Module 3

  • Compliance with Lebanon MoPH, PIC/S GMP, and WHO GMP requirements

  • Support for:

    • New product registration dossiers

    • Manufacturing site change / site addition approvals

    • Post-approval changes & lifecycle management

    • Export dossiers for GCC, Africa & ROW markets

  • Tech Transfer documentation for MoPH inspections & GMP audits

🛡️ Post-Transfer & Operational Support

  • Handling MoPH / authority queries related to technology transfer

  • Deficiency response preparation with 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 Lebanon

  • Pharmaceutical manufacturers

  • Local and regional CMOs

  • Importers and marketing authorization holders (MAHs)

  • Technology licensors & transfer partners

  • Export-oriented pharma companies

Lebanon & Global Regulatory Alignment

Our Tech Transfer services are designed to meet Lebanon MoPH requirements while remaining fully aligned with international regulatory standards, including:

  • Lebanon MoPH

  • PIC/S GMP

  • WHO GMP

  • ICH Guidelines (Q8, Q9, Q10)

  • GCC / EU regulatory expectations (where applicable)

Why Clients Serving Lebanon Choose PharmaTechXfer

✅ 150+ FDP Tech Transfer projects completed
✅ Since 2008 Middle East & global regulatory experience
✅ MoPH & PIC/S-aligned documentation
✅ End-to-end tech transfer lifecycle support
✅ Strong regulatory query & deficiency handling
✅ Proven, inspection-friendly approach

Our Approach

Scientific. Structured. Regulator-Focused.

  1. Product & process understanding

  2. Gap analysis between sending & receiving site

  3. Customized Tech Transfer strategy

  4. GMP & MoPH-aligned documentation

  5. 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 Middle East, Asia, Africa, and regulated global markets, including Lebanon