GlobalCOA – Cyprus

Certificate of Analysis (COA) Preparation, Review & Testing Services

Cyprus-Compliant COAs. EU-Aligned. Regulatory-Ready. Export-Focused.

GlobalCOA, a professional service brand of Zoesoe Exports Pvt Ltd, provides end-to-end Certificate of Analysis (COA) preparation, review, and testing coordination services in accordance with Republic of Cyprus and European Union regulatory requirements for products manufactured in Cyprus or imported into / exported from Cyprus.

We support Cypriot manufacturers, EU importers, exporters, distributors, CMOs, and international brand owners with accurate, compliant, and authority-acceptable COAs, ensuring smooth approval by Cypriot authorities and full EU regulatory acceptance.

Regulatory Framework – Cyprus

GlobalCOA services are aligned with the regulatory and quality requirements of:

Pharmaceutical Services, Ministry of Health – Cyprus
Cyprus Medicines Council
European Medicines Agency (EMA)
European Pharmacopoeia (Ph. Eur.)
State General Laboratory (SGL) – Cyprus
EU GMP / GDP requirements
ISO/IEC 17025-accredited testing laboratories (EU-recognized)

Our GlobalCOA Services – Cyprus

We offer complete lifecycle support for Certificate of Analysis documentation as per Cypriot and EU regulatory expectations:

COA Preparation (Cyprus & EU-Compliant)

• COA drafting as per European Pharmacopoeia (Ph. Eur.), Cyprus Pharmaceutical Services, and EMA requirements
• Alignment with USP / BP / IP for non-EU imports and global exports
Batch-wise, stability-based, and customer-specific COAs
• COAs suitable for:
– Cyprus Medicines Council & EMA product registrations
– EU import release & batch certification
– Export shipments
– Distributor, tender, and partner submissions

COA Review & Regulatory Compliance Assessment

• Review of existing COAs for Cyprus MoH / EMA / EU GMP compliance
• Identification and correction of:
– Missing mandatory parameters
– Incorrect specifications or acceptance limits
– Unsupported non-pharmacopoeial test methods
• Harmonization with:
– Product specifications
– CTD / eCTD dossiers
– DMFs / ASMFs
– Manufacturing authorizations and batch documentation

Testing & Analytical Coordination – Cyprus / EU

• Testing coordination through EU-recognized ISO/IEC 17025-accredited laboratories
• Method selection based on:
– European Pharmacopoeia (Ph. Eur.)
– EMA / ICH-aligned analytical methods
– USP / BP (where accepted)
– Validated in-house methods with scientific justification
• Support for:
– Re-testing and verification
OOS / OOT investigations
– Trend analysis and regulatory justifications

Product Categories Covered – Cyprus

GlobalCOA provides COA services for a wide range of regulated products:

🔹 Raw Materials

• APIs and pharmaceutical actives
• Excipients
• Herbal and botanical raw materials
• Chemical intermediates

🔹 Packaging Materials

• Primary pharmaceutical packaging
• Secondary and tertiary packaging
Food-contact and cosmetic-contact materials (EU-compliant)

🔹 Finished Products

• Pharmaceutical formulations & APIs
• Biotechnology & biologics products
• Vaccines & advanced therapies
• Cosmetics & personal care products
• Nutraceuticals, food ingredients, and dietary supplements

🔹 Solvents & Processing Aids

• Residual and recovery solvents
• Cleaning and processing solvents
• Industrial and laboratory solvents

Industries We Serve – Cyprus

GlobalCOA supports regulated industries across Cyprus, including:

• Pharmaceuticals & APIs
• Biotechnology & Life Sciences
• Contract Manufacturing Organizations (CMOs)
• Cosmetics & Personal Care
• Herbal & Traditional Medicines
• Food & Nutraceutical Ingredients
• Specialty & Industrial Chemicals

Why Choose GlobalCOA for Cyprus?

✔ Strong understanding of Cyprus MoH, EMA & EU regulatory expectations
✔ COAs aligned with European Pharmacopoeia and ICH guidelines
✔ Seamless coordination with EU-accredited laboratories
EU-ready and export-ready COAs
✔ Audit-ready, inspection-friendly documentation
✔ Backed by the regulatory expertise of Zoesoe Exports Pvt Ltd

Regulatory & Export Support – Cyprus

GlobalCOA COAs support:

• Cyprus Medicines Council & EMA product registrations and lifecycle variations
• EU batch release & QP-related documentation
• Import/export clearance within and outside the EU
• CTD / eCTD & ASMF submissions
• Distributor, partner, and tender requirements
• Regulatory inspections and quality audits

Our Cyprus-focused COAs help reduce regulatory queries, prevent batch delays, and ensure uninterrupted EU market access.

Get Started with GlobalCOA – Cyprus

Whether you require new COA preparation, review of existing COAs, or testing coordination for products manufactured in or exported from Cyprus, GlobalCOA by Zoesoe Exports Pvt Ltd is your trusted EU compliance partner.

📩 Contact us today to discuss your product category, Cypriot / EU regulatory pathway, and COA requirements.