Year: 2025
Type: article
Abstract: 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.
Source: Pravo - teorija i praksa
DOI: 10.5937/ptp2501055k
Language: English
Topic: Healthcare Regulation
Subfield: Health Information Management
Field: Health Professions
Domain: Health Sciences
Open Access status: diamond
OpenAlex ID: W4409247489