We have extensive regulatory experience and presence in the UAE. Our business model enables us to keep overheads low while at the same time our team’s regulatory expertise in product registration and post-marketing services adds significant value to our clients.
Although, every country's health authority has different regulatory requirements and processes, fortunately, most of the GCC countries, have a uniform system of registration for pharmaceutical, herbal, medical devices as well as General List items. Therefore, registering a product in the UAE renders significant advantage for its ongoing registration in other neighboring countries. Medblend, can serve as your regulatory liason with the UAE Ministry of Health to manage and support documentation preparation and submission on your behalf. By partnering with Medblend, you can concentrate your resources on R&D and developing new products, instead of worrying for regulatory follow-ups and documentations. In addition, many companies finding it difficult to give due attention to their older products that have been in the market for quite sometime, being aware that these need to be re-registered and their documentation to be updated regularly.
Medblend, can assist you to shoulder regulatory affairs and support tasks and even negotiate on your behalf with selected regulatory agencies.