The phrase "authorized product" is correct and usable in written English.
It can be used to refer to a product that has been officially approved or sanctioned by a governing body or organization.
Example: "Only authorized products are allowed to be sold in this store to ensure quality and safety."
Alternatives: "approved product" or "certified product".
Ivomec® oral was considered the reference product (RF) as it was the pioneer first authorized product with a full dossier (NADA 131 392; approval date: July 26 , 1988.
And even as investigators seize millions of illicit CDs, the big labels' own attempts to recreate the fast and loose feel of mixtapes in an authorized product have stumbled.
New European Union rules that went into effect in 2007 for the first time specifically authorized product placement, which had already been practiced in E.U. countries, like Spain, Italy and Austria, under liberal interpretations of previous laws.
(84%), while 13% contained three and 3.1% contained four a.s., 161 of the 247 combination products were originally authorized products, while 86 products represent subsequent authorizations under a different trade name.
Currently, Switzerland is re-evaluating authorized products and further RAC values will be published in the coming years.
Given the fact that the safety profile of newly authorized products is not well established, a carefully designed pharmacovigilance program is particularly important at the early stages of drug authorization [ 22].
Excluding the 26 combination products that are used for seed treatment, the remaining 135 originally authorized combination products belong mainly to two groups: 69 products containing only herbicidal a.s. and 58 products containing only fungicidal a.s.s
Therefore, authorized efficient products, economically available for the farmer, able to enhance plant growth and soil nutrients availability are needed.
Such tests became obligatory for newly authorized medicinal products [ 3, 4].The purpose of user testing is to achieve legible, clear and easy to use package leaflets [ 3].
In comparison to newer products, products authorized for more than 10 years contained significantly fewer potential safety concerns (60 vs. 92 %; p < 0.01) and required fewer SPC changes (15 vs. 46 %; p = 0.03).
The MEB is responsible for authorising and monitoring safe and effective medicinal products on the Dutch market, and shares in the responsibility for authorizing medicinal products throughout the European Union.
