🇫🇷 Regulatory Affairs Services in France
REGULATORY NEXUS GLOBAL
Regulatory Affairs Solutions for Pharmaceutical, Nutraceutical, Herbal and Cosmetic Products in France
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 France and across the European Union.
France is one of the largest pharmaceutical markets in Europe and a member of the European Union. Pharmaceutical and healthcare product registrations must therefore 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 France and other EU member states.
Regulatory Authority in France
Medicinal products in France are regulated by the National Agency for the Safety of Medicines and Health Products (ANSM).
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 French regulatory requirements.
Our Mission
Our mission is to simplify regulatory compliance for the French and European pharmaceutical markets and enable companies to successfully register and commercialize pharmaceutical, nutraceutical, herbal and cosmetic products in France and across the European Union through scientifically sound regulatory documentation.
Core Regulatory Services for France
EU-CTD Dossier Preparation
Pharmaceutical product registration in France 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 France 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 France
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 France must comply with EU food supplement regulations and French national 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 France 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 France
Through France, companies can access the entire European pharmaceutical and healthcare market.
REGULATORY NEXUS GLOBAL supports regulatory documentation for EU countries including:
• Germany
• Italy
• Spain
• Belgium
• Austria
• Poland
• Denmark
• Sweden
• Finland
• Ireland
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 France, the European Union and other regulated global markets.