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Hotel and cosmetics: regulatory aspects

In the summer, everyone needs to recharge their energy with a nice holiday, especially in this period, when the pandemic...

European Authorized Representative for Medical Devices: from old Directive 93/42/EEC to new Regulation 2017/745

What kind of responsibility has a European authorised representative of medical devices? The response is in the text of Regulation 2017/745...

N-nitrosamine contamination in drugs: European Pharmacopoieia review and practical applications

N-nitrosamines are organic compounds that are possibly carcinogenic to humans. They are contained in some foods, in drink water supplies, and some classes...

Switzerland – EU: MRA and Swiss authorised representative

The agreement 0.946.526.81 on the mutual recognition of conformity assessment (MRA) has made easier, in the last 22 years, the free exchange...

Food additives, flavours and enzymes: new operative procedures for EFSA authorisations

Food additives, flavours and enzymes are three categories of substances entering and playing a crucial role in the manufacturing chain of foods. The...

I Botanicals

Botanicals and dossier, the use of plants in food supplements is still regulated nationally

At the European level, the concept of “botanicals” is well known and has given rise to interesting cooperation projects between...

The importance of standards for translations

In a globalised world, harmonisation and standards are key elements allowing the acceptance and circulation of goods, systems, methods and applications. A standard is...

The marketing of veterinary drugs

The marketing of veterinary medicinal products is subject to the release of the relevant authorisation by the competent authority. In...

The qualifications of specialised translators

The translation of specialised texts generally requires a deep linguistic competence (both in the source and target language), a good...

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