PharmaTechXfer Global Technical Transfer (Tech Transfer) Services for Finished Dosage Products (FDP) – Latvia
Regulatory-Compliant | Authority-Ready | 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, CMOs, CDMOs, and Marketing Authorisation Holders serving Latvia.
Since 2008, we have successfully supported 150+ FDP technology transfer projects across highly regulated global markets, ensuring smooth scale-up, EU-GMP-compliant documentation, and inspection-ready commercial manufacturing.
We support companies manufacturing within Latvia as well as international manufacturers exporting finished dosage products to Latvia and the wider European Union market.
Who We Are
PharmaTechXfer is a specialised pharmaceutical technology transfer service provider, focused exclusively on Finished Dosage Product (FDP) Tech Transfer documentation, execution support, and regulatory query handling.
We bridge critical transitions between:
• R&D → Pilot → Commercial manufacturing
• Sending site → Receiving site (Latvia or overseas)
• Development → Regulatory approval → Commercial supply
All activities are delivered by experienced pharmaceutical technologists, QA professionals, and regulatory experts, ensuring EU-GMP-compliant, SAM-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)
• Process control strategy with CPP / CQA mapping
• Equipment equivalency, comparability & scale-up justification
• Packaging, labelling & artwork transfer documentation
🏭 Manufacturing & Process Transfer Support
• R&D to commercial scale technology transfer
• Site-to-site tech transfer (Latvia ↔ global manufacturing sites)
• Equipment mapping, gap analysis & process optimisation
• Scale-up & validation readiness (PPQ / process validation support)
• Risk assessment based on ICH Q9
📑 Regulatory-Aligned Tech Transfer
• Tech Transfer documentation aligned with CTD / eCTD Module 3
• Compliance support aligned with Latvian State Agency of Medicines (SAM / ZVA) & EU requirements
• Support for MAA, variations, and manufacturing site changes
• Tech Transfer documentation for EU-GMP inspections & audits
🛡️ Post-Transfer & Operational Support
• Handling SAM / EU authority queries related to tech transfer
• Deficiency response preparation & scientific justifications
• Change control & post-approval documentation
• Lifecycle management & variation support
• Inspection readiness assistance
Dosage Forms We Support
• Tablets (IR, MR, ER, EC)
• Capsules (Hard gelatin & HPMC)
• Oral liquids & suspensions
• Dry syrups
• Powders & granules
• Semi-solids (where applicable)
Industries & Clients We Serve in Latvia
• Pharmaceutical manufacturers
• Contract Manufacturing Organizations (CMOs / CDMOs)
• Marketing Authorisation Holders (MAHs)
• Importers & distributors supplying the Latvian & EU market
• API-to-FDP expansion companies
• Export-focused manufacturers targeting regulated markets
Regulatory & Compliance Alignment
Our Tech Transfer services are aligned with Latvian and EU regulatory expectations, including:
• Latvian State Agency of Medicines (SAM / ZVA) GMP & dossier requirements
• EU CTD / eCTD Module 3 expectations
• EU-GMP & PIC/S principles
• Reliance on EU-GMP / US FDA inspection standards
Aligned with:
• ICH Guidelines (Q8, Q9, Q10)
• EU-GMP
• WHO GMP
• US FDA
Why PharmaTechXfer?
✅ 150+ FDP Tech Transfer projects completed
✅ Global regulatory experience since 2008
✅ EU-GMP & SAM-aligned, authority-ready documentation
✅ Strong expertise in regulated-market site transfers
✅ End-to-end lifecycle & post-approval support
✅ Proven inspection-friendly approach
Our Approach
Scientific. Structured. Regulator-Focused.
Comprehensive product & process understanding
Gap analysis between sending & receiving sites
Customized Tech Transfer strategy
EU-GMP & SAM-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 highly regulated and semi-regulated markets, including Latvia and the European Union.