Strategic Regulatory Partner for Success in Oman

  • Tailored Regulatory Support
  • Product Maintenance & Compliance
  • Flexible Regulatory Teams

Greetings from
Freyr Oman

With a growing healthcare market, Oman offers strong opportunities for medicinal products and consumer manufacturers. Under the Ministry of Health (MOH), the Directorate General of Pharmaceutical Affairs and Drug Control (DGPA&DC) serves as the national Regulatory authority for medicinal products, food and food supplements, and related health products.

Cosmetic products in Oman are primarily governed by GCC technical regulations issued by the Gulf Standardization Organization (GSO) and enforced by the Ministry of Commerce and Industry Oman. These regulations ensure that only safe, high-quality, and compliant products are placed in the market. Oman follows GCC harmonized cosmetic regulations, particularly GSO 1943, which outlines safety, labeling, and Ingredient requirements for cosmetic and personal care products

In Oman, biocides and disinfectants must be registered with the Ministry of Health for safety, while detergents require environmental permits and formulation registration through the Environment Authority. To access the Omani market, manufacturers must comply with applicable requirements, including product registration, dossier submissions, and labelling obligations

As a global Regulatory partner, Freyr provides end-to-end support across pharmaceuticals, cosmetics, food and food supplements, chemicals, household products, and detergents, ensuring timely approvals and helping businesses achieve compliant and efficient market entry.

Industries We Serve in Oman

The Directorate General of Pharmaceutical Affairs and Drug Control (DGPA&DC), under the Ministry of Health (MOH), is the sole authority for pharmaceuticals in Oman. DGPA&DC oversees product registration, dossier review, Good Manufacturing Practice (GMP) compliance, and market authorization processes.

Freyr Solutions provides end-to-end Regulatory support in Oman, including gap analysis, dossier preparation, submission strategy, and authority liaison, helping companies achieve timely approvals and efficient market entry.

Freyr Offerings

  • End-to-end pharma product registration support, including dossier preparation, submission, and follow-up
  • Regulatory strategy & intelligence support for timely approvals

Freyr Advantages

  • Local expertise with deep knowledge of Omani regulations
  • Global experience ensuring smooth, multi-market submissions
  • Proactive, structured approach minimizing delays and risks
  • Comprehensive support from registration to post-approval compliance

Looking for Regulatory Support in Oman

Contact us now for Expert Guidance and Support