Annual Meeting 2022 – Gruppo FarmaImpresa

The annual meeting of Gruppo FarmaImpresa was held on February 10, 2022. CEO Daniele Scetta outlined the achievements to date and shared the goal plan for the next three years. Gruppo FarmaImpresa thanks each of its employees for their commitment, “Because a company is only as good as the people in it.” #WeAreGruppoFarmaImpresa

CPHI Frankfurt 2022

CPHI Frankfurt 2022 has ended, it has been 3 days full of emotions, networking and warmth. We want to thank all our customers who visited us at the booth and all the people who stopped by. It was a wonderful experience again this year. See you again next year, ready for a new adventure!

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…