Vertaling van "the general public be given detailed information " (Nederlands → Frans) :

The Ministry of Public Health has, however, requested that a post-consumption follow-up be carried out and that the general public be given detailed information about the product’s adverse effects.
Le Ministère de la Santé a cependant demandé que soit mis en œuvre un suivi post-consommation et une information précise à l’attention du grand public sur les effets indésirables de ce produit.

Proactive contacts with the general and specialised press, various publications and information campaigns will be included together with future internal communication actions in a proper communication plan so as to implement a strategic communication policy as quickly as possible.
Proactive contacts with the general and specialised press, various publications and information campaigns will be included together with future internal communication actions in a proper communication plan so as to implement a strategic communication policy as quickly as possible.

The BUM department is legally required to provide support with putting online the list of medicines authorised in Belgium for new medicine MA and of the official information (Summary of Product Characteristics for healthcare professionals and leaflet for the general public).
The BUM department is legally required to provide support with putting online the list of medicines authorised in Belgium for new medicine MA and of the official information (Summary of Product Characteristics for healthcare professionals and leaflet for the general public).

De Europese Commissie heeft een voorstel tot “Directive of the European Parliament and of the Council amending, as regards information to the general public on medicinal products subject to medical prescription, Directive 2001l83/EC on the Community code relating to medicinal products for human use” goedgekeurd (bijlage).
La Commission européenne a déposé une proposition de “Directive of the European Parliament and of the Council amending, as regards information to the general public on medicinal products subject to medical prescription, Directive 2001/83/EC on the Community code relating to medicinal products for human use” (cf. annexe).