🇸🇨 Regulatory Affairs Services in Seychelles
REGULATORY NEXUS GLOBAL
Regulatory Affairs Solutions for Pharmaceutical, Nutraceutical, Herbal and Cosmetic Products in Seychelles
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 Seychelles.
The Seychelles pharmaceutical market is relatively small but highly dependent on imported medicines and healthcare products. Companies exporting pharmaceutical, nutraceutical, herbal and cosmetic products to Seychelles must comply with national regulatory requirements, product registration procedures, and technical documentation standards before products can be marketed.
REGULATORY NEXUS GLOBAL assists international manufacturers by preparing Seychelles-compliant regulatory dossiers, technical documentation and export registration files required for successful product approval and market entry.
Regulatory Authority in Seychelles
Medicinal products and healthcare products in Seychelles are regulated by the Seychelles Medicines Regulatory Authority (SMRA).
The authority evaluates product quality, safety, efficacy, manufacturing standards and regulatory documentation before granting product registration and import authorization.
REGULATORY NEXUS GLOBAL supports companies in preparing regulatory dossiers aligned with SMRA regulatory guidelines and international pharmaceutical standards such as ICH and WHO requirements.
Our Mission
Our mission is to simplify regulatory compliance for the Seychelles pharmaceutical and healthcare market and enable companies to successfully register and market pharmaceutical, nutraceutical, herbal and cosmetic products in Seychelles through scientifically sound regulatory documentation.
Core Regulatory Services for Seychelles
Pharmaceutical Product Registration Dossiers
We prepare regulatory documentation required for pharmaceutical product registration and import approval in Seychelles.
Our services include:
• Administrative regulatory documentation
• Product formulation and specification documentation
• API and manufacturing documentation
• Stability study documentation
• Quality control and testing documentation
• Bioequivalence documentation (for generic medicines)
All documentation is prepared according to international pharmaceutical regulatory standards and Seychelles regulatory requirements.
Regulatory Services for Multiple Product Categories
Pharmaceutical Products
• Generic drug registration dossiers
• CTD dossier preparation
• API documentation and Drug Master File (DMF) support
• Bioequivalence documentation
• CMC technical documentation
• Stability study documentation
Nutraceuticals & Food Supplements
Nutraceutical products exported to Seychelles must comply with regulatory requirements of the Seychelles Medicines Regulatory Authority and national health authorities.
Our services include:
• Nutraceutical regulatory documentation
• Ingredient compliance verification
• Product formulation documentation
• Export registration documentation
Herbal & Traditional Medicine Products
Herbal medicines must comply with regulatory safety and quality standards before marketing approval.
Our services include:
• Herbal medicine regulatory dossiers
• Botanical ingredient documentation
• Traditional medicine regulatory documentation
• Export regulatory support
Cosmetics & Cosmeceuticals
Cosmetic products marketed in Seychelles must comply with cosmetic safety and ingredient regulations.
Our services include:
• Cosmetic Product Information File (PIF)
• Cosmetic safety documentation
• Cosmetic regulatory compliance documentation
• Ingredient regulatory compliance
Veterinary Products
Veterinary medicinal products must comply with regulatory requirements before importation and distribution.
Our services include:
• Veterinary medicinal product dossiers
• Veterinary regulatory documentation
• Export 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 Seychelles
Africa & Indian Ocean Market Support
REGULATORY NEXUS GLOBAL supports regulatory documentation and product registration across African and Indian Ocean healthcare markets, including:
• Seychelles
• Mauritius
• Madagascar
• Comoros
• Kenya
• Tanzania
• Rwanda
• Ethiopia
• South Africa
Why Choose REGULATORY NEXUS GLOBAL
✔ Experienced regulatory affairs professionals
✔ Expertise in international regulatory documentation
✔ Support for pharmaceuticals, nutraceuticals, herbal and cosmetics
✔ Reliable scientific documentation
✔ End-to-end regulatory solutions for global export 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 Seychelles and other regulated global markets.