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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?? 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