🇲🇺 Regulatory Affairs Services – Mauritius

REGULATORY NEXUS GLOBAL

Mauritius Regulatory Affairs Solutions for Pharmaceutical, Nutraceutical, Herbal and Cosmetic Products

REGULATORY NEXUS GLOBAL is a specialized scientific and regulatory division of Zoesoe Exports Pvt Ltd, providing professional regulatory affairs services and product registration support for Mauritius.

We assist pharmaceutical, nutraceutical, herbal, veterinary and cosmetic companies in navigating the Mauritian regulatory framework and successfully registering their products for the Mauritian market.

Our regulatory specialists provide complete regulatory documentation, dossier preparation and submission support aligned with Mauritius regulatory authority requirements.

Mauritius Regulatory Authority

Pharmaceutical products and healthcare products in Mauritius are regulated by the Mauritius Medicines Regulatory Authority (MMRA).

The authority operates under the Ministry of Health and Wellness Mauritius and is responsible for:

• Pharmaceutical product registration and marketing authorization
• Regulation of medicines, biological products and medical devices
• Licensing of pharmaceutical manufacturers, importers and distributors
• Monitoring drug quality and safety
• Pharmacovigilance and post-marketing surveillance
• Regulation of cosmetics and healthcare products

REGULATORY NEXUS GLOBAL provides regulatory documentation and compliance support aligned with MMRA regulatory requirements.

Our Mission

To simplify Mauritius regulatory compliance and enable companies to successfully register and market their products in Mauritius through scientifically sound and compliant regulatory documentation.

Our Core Regulatory Services for Mauritius

Pharmaceutical Product Registration

We prepare Mauritius-compliant pharmaceutical regulatory dossiers for submission to the Mauritius Medicines Regulatory Authority.

Our services include preparation of:

• Administrative documentation
• Product formulation and composition details
• Manufacturing process documentation
• Quality control specifications and analytical methods
• Stability study reports
• Certificate of Pharmaceutical Product (CPP) documentation
• GMP documentation
• Bioequivalence documentation (where required)

All dossiers are prepared according to Mauritian regulatory guidelines and international regulatory standards.

CTD Dossier Preparation

Pharmaceutical product registration in Mauritius generally follows documentation structured according to the **Common Technical Document (CTD) format.

Our CTD dossier preparation services include:

Module 1 – Administrative Information (Mauritius-specific requirements)
Module 2 – Quality Overall Summary (QOS)
Module 3 – Quality / CMC Documentation
Module 4 – Non-Clinical Study Reports
Module 5 – Clinical / Bioequivalence Study Reports

Our regulatory experts ensure dossiers comply with ICH guidelines, WHO standards and MMRA regulatory expectations.

Pharmaceutical Registration Process in Mauritius

The general process for pharmaceutical product registration in Mauritius includes:

  1. Appointment of a local Mauritian marketing authorization holder or importer.

  2. Submission of CTD regulatory dossier and legal documentation to the Mauritius Medicines Regulatory Authority.

  3. Technical evaluation of product quality, safety and efficacy.

  4. Laboratory testing and regulatory review.

  5. Approval and issuance of marketing authorization for Mauritius.

The registration process typically takes 8–12 months depending on product category and regulatory review timeline.

Regulatory Services for Multiple Product Categories in Mauritius

Pharmaceuticals

• Generic drug registration dossiers
• API documentation and DMF support
• Bioequivalence documentation
• CMC documentation
• Stability study documentation
• GMP compliance documentation

Nutraceuticals & Food Supplements

Mauritius has a growing market for nutraceutical and dietary supplement products.

Our services include:

• Food supplement regulatory documentation
• Ingredient regulatory compliance verification
• Label compliance documentation
• Export regulatory documentation

Herbal & Traditional Products

Herbal and traditional medicine products are also present in the Mauritian healthcare market.

We provide regulatory documentation support including:

• Herbal product regulatory dossiers
• Traditional medicine documentation
• Ingredient safety documentation
• Export registration support

Cosmetics & Personal Care Products

Cosmetic products marketed in Mauritius must comply with national cosmetic safety and regulatory requirements.

Our services include:

• Cosmetic Product Information File (PIF) preparation
• Ingredient regulatory compliance verification
• Cosmetic product registration documentation
• Product safety documentation

Veterinary Products

• Veterinary drug regulatory dossiers
• Product technical documentation
• Export regulatory documentation

Additional Regulatory Support

REGULATORY NEXUS GLOBAL also provides:

• Technical scientific document writing
• Product development documentation
• Analytical method validation documentation (ICH Guidelines)
• Clinical trial and bioequivalence documentation
• Regulatory gap analysis
• Regulatory strategy planning
• Export registration support for Mauritius

Mauritius Market Entry Support

Our regulatory experts assist companies seeking to enter the Mauritian pharmaceutical and healthcare market through:

• Regulatory documentation preparation
• CTD-compliant dossier development
• MMRA regulatory submission support
• Import/export regulatory documentation
• Market entry regulatory consulting

Why Choose REGULATORY NEXUS GLOBAL

✔ Experienced regulatory affairs professionals
✔ Expertise in African regulatory requirements
✔ ICH-compliant regulatory documentation
✔ Support from product development to registration
✔ Reliable scientific documentation
✔ End-to-end regulatory solutions

About REGULATORY NEXUS GLOBAL

REGULATORY NEXUS GLOBAL operates as the scientific regulatory arm of Zoesoe Exports Pvt Ltd, providing global regulatory consultancy, export support and regulatory documentation services for pharmaceutical, herbal, nutraceutical and cosmetic products across international markets.