Opinjonijiet fejn membri tal-Grupp ta’ Min Iħaddem huma relatur/korelatur/relatur ġenerali

Pages

Displaying 1 - 10 of 812
Għaddejjin (updated on 01/12/2023)
Referenza: 
NAT/880-EESC-2023
Sessjoni plenarja: 
583 -
Dec 13, 2023 Dec 14, 2023

Opinjoni mressqa mis-sezzjoni tal-KESE: Regulation on circularity requirements for vehicle design and end-of life vehicle (ELV) management

Għaddejjin (updated on 30/11/2023)
Referenza: 
NAT/915-EESC-2023
Sessjoni plenarja: 
583 -
Dec 13, 2023 Dec 14, 2023

Opinjoni mressqa mis-sezzjoni tal-KESE: Advancing the EU's just transition policy framework: what measures are necessary

Għaddejjin (updated on 29/11/2023)
Referenza: 
INT/1042-EESC-2023
Sessjoni plenarja: 
583 -
Dec 13, 2023 Dec 14, 2023

This initiative aims at providing detailed rules to support the smooth functioning of the cooperation and consistency mechanism established by the General Data Protection Regulation (GDPR).

Opinjoni mressqa mis-sezzjoni tal-KESE: GDPR - additional procedural rules

Għaddejjin (updated on 28/11/2023)
Referenza: 
NAT/894-EESC

Microplastics are persistent, very mobile, and hard to remove from nature. Microplastics are widespread in the world and in the human body, and a cause of growing concerns. Plastic pellets are found in water and soil, including agricultural lands, and harm ecosystems and biodiversity. Plastic pellets are the one of the largest sources of unintentional microplastic pollution.

For the first time, the European Commission proposes measures to prevent microplastic pollution from the unintentional release of plastic pellets.

Għaddejjin (updated on 22/11/2023)
Referenza: 
CCMI/212-EESC-2023
Sessjoni plenarja: 
583 -
Dec 13, 2023 Dec 14, 2023

The Covid 19-pandemic has drawn attention to the role of the pharmaceutical industry and to production, availability and affordability of medicines and medicinal products on the European market.

Dependency on critical ingredients, such as active pharmaceutical ingredients (APIs), became obvious when China and India limited exports. According to current data, up to 80% of APIs used in Europe and about 40% of finished medicines sold in Europe come from China or India. The European Union's increasing dependence on API supplies has led to a partial loss of capability to manufacture active substances independently, which poses a potential threat to public health in the countries of the European Union.

Opinjoni mressqa mis-sezzjoni tal-KESE: Securing Europe’s medicine supply: envisioning a Critical Medicines Act

Pages