MOHAP is the primary regulatory body in the UAE, responsible for setting standards and regulations for medical devices, pharmaceuticals, and cosmetics. Its mission is to enhance the quality of products and ensure consumer safety.
Our services in UAE for Pharmaceuticals:
The authority regulates the approval process for pharmaceuticals, ensuring that all products are tested for safety and efficacy before market introduction.
- Regulatory Compliance and Approval:
Navigate and comply with regulatory requirements in the UAE.
Expertise in ensuring seamless regulatory approval processes for pharmaceutical and medical products.
- Local Regulatory Affairs Services:
Tailored support for the unique regulatory landscape of the UAE.
Specialized guidance to streamline local compliance and ensure adherence to regional regulations.
- CMC (Chemistry, Manufacturing, and Controls) Regulatory Affairs:
Comprehensive services ensuring compliance with CMC regulations.
Detailed oversight and support for the documentation and submission of CMC-related requirements.
- Publishing Regulatory Affairs Activities:
Efficient handling and submission of regulatory documents for approval.
Ensuring timely and accurate submission of regulatory paperwork to relevant authorities.
- Data Entry on Client Management Systems:
Streamlined data entry services for maintaining accurate and up-to-date information.
Ensuring the integrity of records to support regulatory compliance.
- Regulatory Outsourcing:
Confidential and professional assistance in outsourcing regulatory affairs requirements.
Expert management of your regulatory profile from initiation through to the completion of all regulatory tasks.
- General Pharmaceutical Consultations:
Expert advice and support on a wide range of pharmaceutical regulatory and compliance issues.
Providing strategic guidance and problem-solving for regulatory challenges and opportunities.