Regulatory aspects of the control of dietary supplements in the Republic of Serbia

Автор: Jovana Z. Cicmil, Davor J. Korcok, Nada Trsic Milanovic

Журнал: Pravo - teorija i praksa @pravni-fakultet

Статья в выпуске: 1 vol.42, 2025 года.

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The modern way of life often involves supplementing the diet with dietary supplements. By using them, we introduce additional vitamins, minerals, probiotics, and other substances with nutritional or physiological effects. These supplements are applied in dosage forms, and their safe use requires consistent adherence to regulatory requirements. Aspects of the control of dietary products include guidelines for production conditions, as well as physico-chemical and microbiological testing. Due to the specificity and widespread use of these products, the analysis requirements for product registration, as well as for product controls during the registration period, should be detailed, but also described in a way that enables their practical implementation. Regulatory aspects of statutory and mandatory requirements often differ in Europe, the USA, China, etc. This paper discusses the requirements of domestic regulations and proposals for their additions or corrections.

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Dietary supplements, regulatory aspects

Короткий адрес: https://sciup.org/170209000

IDR: 170209000   |   УДК: 613.2:340.134(497.11)   |   DOI: 10.5937/ptp2501055K

Regulatorni aspekti kontrole dijetetskih suplemenata u Republici Srbiji

Savremeni način života često podrazumeva dopunu ishrane primenom dijetetskih suplemenata. Njihovom primenom unosimo dodatne vitamine, minerale, probiotike i druge supstance sa hranljivim ili fiziološkim efektom. Primenjuju se u doziranim oblicima i za njihovu bezbednu upotrebu neophodna je dosledna primena regulatornih zahteva. Aspekti kontrole dijetetskih proizvoda podrazumevaju uputstva za uslove proizvodnje, fizičko-hemijska i mikrobiološka ispitivanja. Zbog specifičnosti i široke rasprostranjenosti primene ovih proizvoda zahtevi analiza za registraciju proizvoda kao i za kontrole proizvoda tokom perioda registracije treba da budu detaljni, ali i opisani na način koji omogućuje njihovu praktičnu primenu. Regulatorni aspekti propisanih i obaveznih zahteva često se razlikuju u Evropi, SAD, Kini i dr. U ovom radu razmatrani su zahtevi domaće regulative i predlozi za njihove dopune ili korekcije.

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