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Upset stomach? Maybe an indigestion pill. You might consider anti-congestant medication. In the United Arab Emirates, such pharmaceuticals are easy to come by, with the majority of people likely to have a supply already to hand in their purses or bathroom cabinets. Yet although these common medications are not controlled in the same manner as prescription drugs, various approvals are required with regards to the importation, sale and marketing of such produce in order to ensure that the drugs we buy over the counter are compliant with UAE standards, thus ensuring our safe consumption. So is the registration of over the counter drugs as simple as the process of procuring and consuming them? Article 65 goes so far as to specify that this includes imported pharmaceuticals, whether or not they have been approved and registered in their country of origin. The decision as to whether to register such products shall be at the discretion of the Ministry of Health following application — and as the criteria on which such a decision will be made is unavailable to the public it appears as though any entity applying for the registration of a product shall have very little guidance to follow in order to increase the likelihood of success. A reading of the applicable section of the Pharmacy Law would give the understanding that Ministry of Health registration is a strict condition to which all pharmaceutical products sold within the UAE must adhere without exception. How is a potential importer supposed to know whether or not his product will require registering pursuant to Article 65? Do such items fall within the remit of the Pharmacy Law and its requirements? And despite the fact that it still does not suggest any composition criteria, the Circular goes some way towards laying out the various administrative requirements that a product should meet in order to obtain a successfully registered status. Further to this the application for registration will require the submission of various supporting documentation on the letterhead of the company requesting the registration of the product complete with the company logo, stamp and authorized signature , which includes but is not limited to:. When submitting a product containing an ingredient derived from animal source the company must go so far as to specify the kind of animal and specifications of the part extracted from it, and must additionally clearly note the percentage of alcohol if any , together with an explanation as to why such ingredients were incorporated;. Tippy tippy tap…Каков ваш цвет?? Черная тоска, покраснеть от гнева, позеленеть от зависти при виде соседской голубой машины… Цвета используются для описания эмоций мы испытываем, и они крайне важны в…. We have already highlighted in a previous article1 the fact that the Federal Law no. Draft with care! What exactly do you mean by medical malpractice? All doctors and medical practitioners have an obligation to their patients to ensure that they are providing a certain…. Medicinal Product Regulation and Product Liability in the United Arab Emirates: An Overview What are the main legislation and regulatory authorities for pharmaceuticals in your jurisdiction? Response: Applicable Legislation: …. Employment in the United Arab Emirates is a frequently discussed area of law and there are several publications that have addressed various aspects of the same. In this article, we…. Recipes are by nature derivative and meant to be shared - that is how they improve, are changed, how new ideas are…. Diageo, a company more commonly associated with alcoholic beverages Smirnoff, Guinness and Johnnie Walker in the United Kingdom- held almost A documentary credit or a letter of credit is usually used to finance international trade. Most documentary…. Агентские соглашения «Если вы строите каждую сделку и отношения в бизнесе и жизни, руководствуясь принципами взаимной выгоды, справедливости и правды, то прибыль не заставит себя ждать». Это высказывание нужно принять…. Published on : 21 May When submitting a product containing an ingredient derived from animal source the company must go so far as to specify the kind of animal and specifications of the part extracted from it, and must additionally clearly note the percentage of alcohol if any , together with an explanation as to why such ingredients were incorporated; Halal certificate issued by recognizable organizations and authorities; Details of a medical storage facility licensed by the Ministry of Health as per the Circular Number 1 of ; Samples of the outer label, inner label and insert of the product; and CD containing artwork outer, inner label and insert of the product. Статьи по Теме. Цвет, цвет, цвет! Регистрация торговых марок цвета. Споры по Закону Коммерческого Агентства We have already highlighted in a previous article1 the fact that the Federal Law no. Письма о намерениях в ОАЭ Draft with care! Medical Negligence - Frequently asked Questions Q1. 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