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Dalla traduzione tradizionale all'addestramento dell'IA
Legal translations 0

From Traditional Translation to AI Training

The translation industry is undergoing a profound and rapid transformation. Until just a few years ago, translation was seen as a fairly linear process—reading the source text, translating it, reviewing it, and delivering the final version. Today, however, the landscape is significantly broader and more dynamic. The introduction of Artificial Intelligence (AI) has opened entirely […]

Tradurre per la SEO
Legal translations 0

SEO Translation: How, Why, and Some Useful Tips

Companies looking to make their mark—and not get lost—in the vast digital ocean of search engines have a powerful ally: SEO translation. This process can transform translated texts into high-quality content that search engines are more likely to display to a global audience. Let’s explore the concept of SEO and its primary goal: The goal […]

Legal translations 0

Patent Litigation: The Crucial Role of Specialized Legal Translations

Patent litigation is a fundamental legal discipline in the field of intellectual property, especially for companies that innovate and want to protect their creations. In this context, legal translation plays a crucial role. While patent litigation primarily involves the defense of exclusive rights related to a patent, globalization has increasingly led to disputes that cross […]

Inclusione e sostenibilità
Legal translations 0

Inclusion, Sustainability, and Tangible Commitment: Aglatech14 Social Project for 2025

At Aglatech14, we believe that a company’s value is not measured solely in numbers but in the tangible impact it creates in society. For this reason, in 2025, we launched an innovative social project based on inclusion, sustainability, and corporate responsibility. Our approach goes beyond simple donations: we actively participate in change, collaborating with organizations […]

Regolamento 2024-1860 per MD e IVD

EU Regulation 2024/1860: Updates for Medical and In Vitro Diagnostic Devices

The EU Regulation 2024/1860, published in the Official Journal of the European Union on July 9, 2024, introduces significant amendments to Regulations (EU) 2017/745 and 2017/746. These amendments include new provisions for the use of the European Database on Medical Devices (EUDAMED) and additional obligations for manufacturers, as explained by Alessandra Basilisco, Biomedical Engineer, Office […]

Italia si adegua a MDR

Italy and the European Regulation on Medical Devices: Balancing Flexibility and Responsibility

Italy has stood out as one of the first European countries to recognize the need to postpone certain deadlines set by the Medical Device Regulation (MDR), thus averting the risk of shortages of essential devices for the European healthcare system. According to Dr. Iachino, Director General of Medical Devices and Pharmaceutical Services at the Ministry […]

Procurement e Health Technology Assessment
Legal translations 0

Procurement and Health Technology Assessment

The integration of procurement and Health Technology Assessment (HTA) is a crucial step toward making purchasing processes more effective and value-based. This was emphasized by Guido Gastaldon, Head of the Healthcare, Goods, and Services Sourcing Division at Consip, during the AboutMedicalDevices conference. This approach is transforming public tenders, particularly in healthcare, making Health Technology Assessment […]

Health Technology Assessment in Italia

Health Technology Assessment (HTA) in Italy

Health Technology Assessment (HTA) in Italy is a multidisciplinary process that synthesizes information on clinical, economic, social, and ethical aspects related to the use of a health technology in a systematic, transparent, unbiased, and robust way. The goal of HTA is to support the definition of safe, effective, and patient-centred health policies, ensuring maximum value […]

Indagini cliniche panorama 2028

Clinical Investigations: The Outlook Towards 2028

With the enforcement of the European Medical Devices Regulation (MDR), clinical evidence has become a cornerstone for regulatory compliance, as highlighted by Pietro Calamea, Director of Office VI – Clinical Investigation of Medical Devices, Directorate General of Medical Devices and Pharmaceutical Services, Ministry of Health, during the AboutMedicalDevices conference. However, contrary to expectations, there has […]