
Search results for 'labelling tablets Italy':
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Section A - Labelling 1. The text of the labelling The Union authorisation of a medicinal product includes the labelling text which is the same throughout the Union. italy: new packaging labelling requirements - toxpartner


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Section A - Labelling 1. The text of the labelling The Union authorisation of a medicinal product includes the labelling text which is the same throughout the Union. Article 9, paragraph 4 (d) of the Regulation provides that must be in annex of the favourable CHMP opinion the draft text of the labelling proposed by the applicant and
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A new requirement for environmental labelling is compulsory for products sold in Italy, according to the Legislative Decree No. 116/2020 dated 3 September 2020.


Obligation for environmental labelling of packaging in Italy. Decree No. 116 of 3 September 2020 obliges actors along the supply chain to label packaging materials. In short, it makes environmental labelling mandatory on all packaging in Italy. The aim of the decree is to reduce the impact of packaging and packaging waste on the environment.


In 2018, as a result, Europe decided to adopt the Directive (EU) 2018/851 concerning waste and Italy has transposed two of the four Directives approving the D.lgs. 116/2020 in September 2020. Italy has transposed the Directive differently than other European Countries. It became mandatory to declare on every detachable part of the packaging:


IMA is a global leader in the design and manufacturing of automatic machinery used in the processing and packaging of pharmaceuticals products. Thanks to its high technological profile and the ability to offer tailor-made solutions, IMA can satisfy the most sophisticated requests of the different reference markets.