🇨🇾 Regulatory Affairs Services in Cyprus
REGULATORY NEXUS GLOBAL
Regulatory Affairs Solutions for Pharmaceutical, Nutraceutical, Herbal and Cosmetic Products in Cyprus
REGULATORY NEXUS GLOBAL is a specialized scientific and regulatory division of Zoesoe Exports Pvt Ltd, providing professional regulatory affairs services for pharmaceutical, nutraceutical, herbal, veterinary and cosmetic companies seeking product registration in Cyprus and across the European Union.
Cyprus is a member of the European Union, and pharmaceutical and healthcare product registrations must comply with European Union regulatory frameworks, including EU-CTD dossier requirements.
REGULATORY NEXUS GLOBAL supports international manufacturers by preparing EU-compliant regulatory dossiers, CTD documentation and scientific technical files required for successful product registration in Cyprus and other EU member states.
Regulatory Authority in Cyprus
Medicinal products in Cyprus are regulated by the Pharmaceutical Services of Cyprus, which operates under the Ministry of Health Cyprus.
Product approvals must comply with the regulatory framework of the European Medicines Agency (EMA) and EU pharmaceutical legislation.
REGULATORY NEXUS GLOBAL assists companies in preparing EU-compliant regulatory dossiers aligned with EMA and Cypriot regulatory requirements.
Our Mission
Our mission is to simplify regulatory compliance for the Cyprus and European pharmaceutical markets and enable companies to successfully register and commercialize pharmaceutical, nutraceutical, herbal and cosmetic products in Cyprus and across the European Union through scientifically sound regulatory documentation.
Core Regulatory Services for Cyprus
EU-CTD Dossier Preparation
Pharmaceutical product registration in Cyprus requires dossiers prepared according to the European Union Common Technical Document (EU-CTD) format.
Our EU-CTD dossier preparation services include:
• Module 1 – EU regional administrative information
• Module 2 – Quality Overall Summary (QOS) and expert reports
• Module 3 – Quality / CMC documentation
• Module 4 – Non-clinical study reports
• Module 5 – Clinical study reports / bioequivalence documentation
All documentation is prepared according to ICH guidelines, EMA requirements and EU pharmaceutical regulations.
EU Regulatory Submission Pathways
Pharmaceutical products in Cyprus may be registered through several EU regulatory procedures:
• Centralized Procedure (CP) via the European Medicines Agency
• Decentralized Procedure (DCP) for multi-country EU approvals
• Mutual Recognition Procedure (MRP)
• National Procedure in Cyprus
REGULATORY NEXUS GLOBAL provides regulatory strategy planning and dossier preparation for all EU registration pathways.
Regulatory Services for Multiple Product Categories
Pharmaceutical Products
• Generic drug EU-CTD dossiers
• API documentation and Drug Master File (DMF) support
• Bioequivalence documentation
• CMC technical documentation
• Stability study documentation
• EU regulatory submission documentation
Nutraceuticals & Food Supplements
Food supplements marketed in Cyprus must comply with EU food supplement regulations and national Cypriot requirements.
Our services include:
• Nutraceutical regulatory documentation
• Ingredient compliance verification
• Product formulation documentation
• Technical regulatory documentation
Herbal & Traditional Herbal Products
Herbal medicinal products must comply with EU regulations including the Traditional Herbal Medicinal Products Directive, regulated under guidance of the European Medicines Agency.
Our services include:
• Herbal medicinal product dossiers
• Botanical ingredient documentation
• Traditional herbal regulatory documentation
Cosmetics & Cosmeceuticals
Cosmetics marketed in Cyprus must comply with EU Cosmetic Regulation (EC) No. 1223/2009.
Our services include:
• Cosmetic Product Information File (PIF)
• Cosmetic safety assessment documentation
• Cosmetic regulatory compliance documentation
• Ingredient regulatory compliance
Veterinary Products
• Veterinary medicinal product dossiers
• Veterinary regulatory documentation
• EU veterinary regulatory compliance support
Additional Regulatory Support
REGULATORY NEXUS GLOBAL also provides:
• Technical document writing
• Product development reports
• Analytical method validation documentation (ICH Guidelines)
• Clinical trial and bioequivalence documentation
• Regulatory gap analysis
• Regulatory strategy planning
• Export registration support for EU markets
EU Market Access via Cyprus
Through Cyprus, companies can access the entire European pharmaceutical and healthcare market.
REGULATORY NEXUS GLOBAL supports regulatory documentation for EU countries including:
• Germany
• France
• Italy
• Spain
• Netherlands
• Belgium
• Austria
• Portugal
• Poland
• Greece
Why Choose REGULATORY NEXUS GLOBAL
✔ Experienced regulatory affairs professionals
✔ Expertise in EU-CTD dossier preparation
✔ Compliance with EMA and EU regulatory frameworks
✔ Regulatory support for pharmaceuticals, nutraceuticals, herbal and cosmetics
✔ Reliable scientific documentation
✔ End-to-end regulatory solutions for EU markets
About Zoesoe Exports Pvt Ltd
REGULATORY NEXUS GLOBAL operates as the scientific regulatory arm of Zoesoe Exports Pvt Ltd, a company engaged in global export consultancy, regulatory affairs services and contract manufacturing coordination for pharmaceutical, herbal, nutraceutical and cosmetic products.
Through its regulatory division, the company provides professional regulatory documentation and international product registration support for Cyprus, the European Union and other regulated global markets.