Category: Industry

New European Regulation 2025/40 on Packaging and Packaging Waste (PPWR) – Key Points and New Developments

by Adrià Soriano | Oct 20, 2025 | Container, Industry, Quality

European Regulation 2025/40 on packaging (PPWR) and packaging waste, known by its acronym PPWR (Packaging and Packaging Waste Regulation), is the new European regulation approved at the end of 2024 and published in January 2025….

Conformity labeling and the new European directives for medical devices (MDR)

by Adrià Soriano | Jun 28, 2021 | Industry, Quality

In the plastic manufacturing industry, we must be aware that health products and plastic packaging for the pharmaceutical sector are of special care, since it is in a continuous state of progress and change in processes. That is why Triana, a pioneer in this sector...

Clean room for the manufacture of sanitary products

by Adrià Soriano | May 5, 2021 | Industry

Any company dedicated to production, regardless of the sector and the products that make up its catalog, must ensure that its processes are carried out in a controlled environment free of any contaminating element. In this way the maximum integrity of the product is...

EU MDR: 5 regulatory requirements to market a medical device

by Adrià Soriano | Apr 24, 2021 | Industry

The EU MDR standard is basic for the professional group involved in the marketing of medical devices. From manufacturers, authorized representatives, importers, or distributors of medical devices in the European Union (EU). These professionals must be up to date with...

EUDAMED database: Traceability and transparency of the CE marking

by Adrià Soriano | Apr 15, 2021 | Industry

The EUDAMED database contains many routine and in vitro diagnostic medical devices from the single market. It also has another role that makes it indispensable. It is a platform that allows interaction between manufacturers and authorities, among other agents...

What is considered a medical device? | Classification

by Adrià Soriano | Jan 10, 2021 | Industry

The concept of a medical device is something whose limits are important to define, especially as they affect the technical and legal field of especially sensitive articles. It is also important, on the one hand, because of their close relationship with medicine and on...

New European Regulation 2025/40 on Packaging and Packaging Waste (PPWR) – Key Points and New Developments

Conformity labeling and the new European directives for medical devices (MDR)

Clean room for the manufacture of sanitary products

EU MDR: 5 regulatory requirements to market a medical device

EUDAMED database: Traceability and transparency of the CE marking

What is considered a medical device? | Classification

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