+Article 10 6.

Article 10 6.

By 1 January 2025, the Commission shall provide for the organisation of exchange of information, experience and best practices between Member States on the implementation of Article 9 and this Article and in particular on:

(a) 

the measures to control the establishment, the recognition and functioning of producer responsibility organisations;

(b) 

the measures to control the compliance of producers with their obligations defined in this Directive;

(c) 

the effective implementation of:

(i) 

the coverage of the costs as referred to in Article 9(1), and

(ii) 

the controls on the methods of calculation of producers’ contributions by the producer responsibility organisation as referred to in Article 9(3), point (c);

(d) 

the exemptions provided for in Article 9(2);

(e) 

any other issue in relation to the effective implementation of Article 9 and this Article;

(f) 

the possible impacts of the application of the requirements referred to in Article 9 on the accessibility, availability and affordability of medicines placed on the Union market.

The Commission shall publish the results of the exchange of information, experience and best practices on those and other relevant aspects and, where relevant, provide recommendations or guidelines, or both, to Member States.

1. Panoramica

,

1.1 Riferimenti

1.2 Requisiti identificati

1.3 Standard correlati

2. Requisiti identificati

Requisiti

3. Standard correlati

Standard