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

MoH-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, MAHs, and regional partners serving the Syrian market.

Since 2008, we have successfully supported 150+ FDP technology transfer projects across Middle East, Asia, Africa, Europe, and Latin America, including projects aligned with Syrian Ministry of Health (MoH) requirements and WHO GMP expectations—ensuring effective 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 Syria, we act as a technical and regulatory bridge between:

  • R&D → Pilot → Commercial manufacturing

  • Sending site (originator / regional / overseas) → Receiving site (Syria)

  • Product development → MoH approval → National supply

All services are delivered by experienced pharmaceutical technologists, QA professionals, and regulatory experts, ensuring GMP-compliant, MoH-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, localization & scale-up 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 (Syria Focus)

  • Tech Transfer documentation aligned with CTD / eCTD Module 3

  • Compliance with Syrian MoH, WHO GMP, and regional regulatory expectations

  • Support for:

    • New product registration dossiers

    • Manufacturing site change / site addition approvals

    • Post-approval changes & lifecycle management

    • Localization and import-substitution projects

  • Tech Transfer documentation for MoH inspections & GMP audits

🛡️ Post-Transfer & Operational Support

  • Handling MoH / 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 Syria

  • Pharmaceutical manufacturers

  • Local and regional CMOs

  • Importers and Marketing Authorization Holders (MAHs)

  • Technology licensors & transfer partners

  • Companies supporting local manufacturing & national medicine supply

Syria & Global Regulatory Alignment

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

  • Syrian Ministry of Health

  • WHO GMP

  • ICH Guidelines (Q8, Q9, Q10)

  • Regional MOH expectations

  • Export market compliance (where applicable)

Why Clients Serving Syria Choose PharmaTechXfer

✅ 150+ FDP Tech Transfer projects completed
✅ Since 2008 Middle East & global regulatory experience
✅ MoH & 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.

  1. Product & process understanding

  2. Gap analysis between sending & receiving site

  3. Customized Tech Transfer & localization strategy

  4. GMP & MoH-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 Syria