Cannabidiol as novel food: EFSA suspends judgment

Safety evaluation of cannabidiol (CBD) in food supplement suspended Given the numerous questions regarding the use of cannabidiol (CBD) in foods and in particular in food supplements, EFSA has published the statement on the safety of cannabidiol (CBD), in which it states that its safety of use, as a novel food, cannot be demonstrated due…

The role of Resveratrol against chronic inflammation

The role of resveratrol in treating inflammation in individuals with cardiovascular disease Chronic inflammation is one of the main factors involved in the development and progression of cardiovascular disease (CVD). Resveratrol is a polyphenol (stilbene polyphenol) with a molecular structure very similar to that of estrogen, which in fact acts as an estrogen agonist, as…

PCOS: effectiveness of green tea in weight loss

Polycystic ovary syndrome (PCOS) is the most common endocrine disorder of the reproductive age. This is a fairly common condition that affects 5-10% of women of childbearing age and can adversely affect metabolism and reproductive capacity. The causes of polycystic ovary syndrome are not yet fully known, but it is believed to be due to…

Anise: benefits and therapeutic properties

Anise: benefits and therapeutic properties Limited and preliminary clinical research has examined the efficacy of anise for diabetes, dysmenorrhea, and menopausal hot flashes. Antioxidant, anti-inflammatory, and antimicrobial properties have also been identified. This narrative review summarizes human and animal studies reporting the potential health benefits of aniseed and highlights areas for future research. More

MDR Regulation: Translation and repackaging activities

With the adoption of European Regulations 2017/745 MDR (Medical Device Regulation) and 2017/746 IVDR (In Vitro Diagnostic Regulation), the regulation for medical devices and in vitro medical devices has changed dramatically. The main objectives of the 2017/745 European MDR (Medical Device Regulation) and IVDR (In Vitro Diagnostic Regulation) are to “establish a robust, transparent, predictable…

Legacy devices: Instructions and clarifications

With the adoption of the European Regulations 2017/745 MDR (Medical Device Regulation) and 2017/746 IVDR (In Vitro Diagnostic Regulation), the regulations for medical devices and in vitro medical devices have changed dramatically. The main objectives of the MDR (Medical Device Regulation) and IVDR (In Vitro Diagnostic Regulation) are to “establish a robust, transparent, predictable, and…

The obligations of importers and distributors under MDR

With the adoption of the European Regulations 2017/745 MDR (Medical Device Regulation) and 2017/746 IVDR (In Vitro Diagnostic Regulation), the regulations for medical devices and in vitro medical devices have changed dramatically. With the MDR (Medical Device Regulation), the figures of economic operators were, at last, regulated; figures that were not fully considered in the…