Regulatory Affairs

At Saba Regulatory, we offer comprehensive regulatory affairs services to cater to all your needs and demands related to global product development, registration, and commercialization. Our expertise lies in providing professional regulatory services that ensure compliance with regulatory standards and guide our clients through the complex regulatory landscape.

Our services are designed to support organizations in every stage of their product development journey. From providing necessary information and pragmatic solutions for newly developed products to assisting with market authorization, we are here to streamline the regulatory process and help enhance the commercial worth of your products.

As part of our regulatory affairs services, we handle submissions to the health authority, ensuring that all necessary approvals and postings are obtained. We also provide support in areas such as CMC (Chemistry, Manufacturing, and Controls) and lifecycle maintenance, enabling organizations to maintain regulatory compliance and stay ahead in the market.

At Saba Regulatory, our global regulatory affairs expertise spans across various industries, including Life Sciences, Consumer Pharma, and Bio-Med. We understand the intricate and varying regulatory standards and can help you successfully introduce your products into new markets while maximizing their value.

In Iraq, we are well-versed in the regulatory landscape and have extensive knowledge of the local requirements and procedures. We work closely with the relevant authorities to ensure that your products meet all regulatory standards and gain the necessary approvals for market entry.