Registering a manufacturing site for medical products in the UAE is a high-level regulatory process that establishes the facility as a legitimate producer of human medicines or medical devices. This service is essential for companies looking to contribute to the UAE’s growing local pharmaceutical industry. The registration process is governed by MOHAP and requires strict adherence to Good Manufacturing Practice (GMP) standards.

Applicants must submit a comprehensive dossier detailing the manufacturing site’s layout, equipment, quality control systems, and the qualifications of the technical staff. Forin Plus provides expert consultancy throughout this complex journey, from the initial site registration to the final product listing.

We assist in preparing for GMP inspections, managing the digital submission through the MOHAP portal, and ensuring that all locally manufactured products meet the same rigorous standards as imported ones. Our service facilitates the growth of local manufacturing, ensuring that your facility becomes a trusted provider of high-quality medical products in the region.