PharmaTechXfer Technical Transfer (Tech Transfer) Services for Finished Dosage Products (FDP) – Côte d’Ivoire

• DPM / ANRMP-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 supplying the Ivorian market.

  Since 2008, we have successfully supported 150+ FDP technology transfer projects across West Africa, Africa, Asia, Middle East, Europe, and Latin America, including projects aligned with Côte d’Ivoire Ministry of Health, Direction de la Pharmacie et du Médicament (DPM) and Agence Nationale de la Régulation Pharmaceutique (ANRMP) expectations, as well as WHO GMP standards—ensuring smooth technology transfer, regulatory acceptance, and sustainable medicine 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 Côte d’Ivoire, we act as a technical and regulatory bridge between:

  • R&D → Pilot → Commercial manufacturing

  • Sending site (regional / overseas) → Receiving site

  • Product development → DPM / ANRMP approval → National & WAEMU supply

  All services are delivered by experienced pharmaceutical technologists, QA professionals, and 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 justification

  • Packaging & labeling technology transfer documentation (French alignment where required)

  🏭 Manufacturing & Process Transfer Support

  • R&D to commercial scale technology transfer

  • Site-to-site technology transfer (West Africa / global sites)

  • Equipment mapping, process optimization & line suitability

  • Scale-up support and process validation readiness

  • Quality Risk Management as per ICH Q9

  📑 Regulatory-Aligned Tech Transfer (Côte d’Ivoire Focus)

  • Tech Transfer documentation aligned with CTD / eCTD Module 3

  • Compliance with DPM / ANRMP, WHO GMP, and WAEMU/UEMOA regional requirements

  • Support for:

    • New product registration dossiers

    • Manufacturing site change / site addition approvals

    • Post-approval variations & lifecycle management

    • Public-sector, tender-based & donor-funded supply dossiers

  • Tech Transfer documentation for authority reviews & GMP inspections

  🛡️ Post-Transfer & Operational Support

  • Handling DPM / ANRMP authority queries related to technology transfer

  • Deficiency response preparation with strong scientific justification

  • Change control documentation

  • Post-approval variation support

  • Audit and inspection 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 Côte d’Ivoire

  • Pharmaceutical manufacturers

  • Importers and Marketing Authorization Holders (MAHs)

  • Regional CMOs and partner manufacturing sites

  • Government, NGO & institutional supply partners

  • Export-oriented pharmaceutical companies supplying WAEMU/UEMOA markets

  Côte d’Ivoire & Global Regulatory Alignment

  Our Tech Transfer services are designed to meet Côte d’Ivoire DPM / ANRMP requirements while remaining fully aligned with international regulatory standards, including:

  • Ministry of Health – Côte d’Ivoire

  • Direction de la Pharmacie et du Médicament (DPM)

  • Agence Nationale de la Régulation Pharmaceutique (ANRMP)

  • WHO GMP

  • ICH Guidelines (Q8, Q9, Q10)

  • WAEMU / UEMOA regional expectations

  Why Clients Supplying Côte d’Ivoire Choose PharmaTechXfer

  ✅ 150+ FDP Tech Transfer projects completed
  ✅ Since 2008 West Africa & global regulatory experience
  ✅ DPM/ANRMP & 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 & WAEMU supply strategy

  4. GMP & authority-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 West Africa, Africa, Asia, Middle East, and regulated global markets, including Côte d’Ivoire.