Vertaling van "the information in advertising " (Nederlands → Frans) :

In close cooperation with Mdeon, the FAMHP has mainly focused on the provision of information to the relevant parties, i.e. companies and healthcare professionals, during this first operational year A “contact point” collects and processes information about actions that may constitute an infringement of the legal requirements about advertising. In terms of advertising for healthcare professionals, attention is particularly being focused at present on the conformity of the legally required information
In close cooperation with Mdeon, the FAMHP has mainly focused on the provision of information to the relevant parties, i.e. companies and healthcare professionals, during this first operational year A “contact point” collects and processes information about actions that may constitute an infringement of the legal requirements about advertising. In terms of advertising for healthcare professionals, attention is particularly being focused at present on the conformity of the legally required information

1974 on the opening, transfer and merger of retail pharmacies Royal decree of 9 July 1984 on the provision of information and advertising relating to medicines Royal decree of 11 January 1993 determining the conditions under which medicines for human use may be supplied in sample form Royal decree of 7 April 1995 on the provision of information and advertising relating to medicines for human use Royal decree of 15 July 1997 on active implantable medical devices, transposing Directive 90/385 EEC (AIMD) Royal decree of 19 December 1997 on the control and analysis of the raw materials used by dispensing chemists Royal decree of 18 March 1999 on medical devices, transposing Directive 93/42/EEC of 14 June 1993 (MDD) Royal decree of 11 July 2003 determining the conditions under which medicines for veterinary use may be supplied in sample form Law of 16 December 2004 modifying the regulations on combating abuses in the promotion of medicines Royal decree of 10 June 2006 establishing the report point referred to in Article 10, § 5, of the law of 25 March 1964 on medicines Royal decree of 23 November 2006 implementing Article 10, § 3, of the law of 25 March 1964 on medicines Royal decree of 25 February 2007 recognising the institutions referred to in Article 10 § 3 of the law of 25 March 1964 on medicines
1974 on the opening, transfer and merger of retail pharmacies Royal decree of 9 July 1984 on the provision of information and advertising relating to medicines Royal decree of 11 January 1993 determining the conditions under which medicines for human use may be supplied in sample form Royal decree of 7 April 1995 on the provision of information and advertising relating to medicines for human use Royal decree of 15 July 1997 on active implantable medical devices, transposing Directive 90/385 EEC (AIMD) Royal decree of 19 December 1997 on the control and analysis of the raw materials used by dispensing chemists Royal decree of 18 March 1999 on medical devices, transposing Directive 93/42/EEC of 14 June 1993 (MDD) Royal decree of 11 July 2003 determining the conditions under which medicines for veterinary use may be supplied in sample form Law of 16 December 2004 modifying the regulations on combating abuses in the promotion of medicines Royal decree of 10 June 2006 establishing the report point referred to in Article 10, § 5, of the law of 25 March 1964 on medicines Royal decree of 23 November 2006 implementing Article 10, § 3, of the law of 25 March 1964 on medicines Royal decree of 25 February 2007 recognising the institutions referred to in Article 10 § 3 of the law of 25 March 1964 on medicines

Supervision of advertising ●● Every advertisement for medicines for human use intended for the general public is checked before publication.
Supervision of advertising ●● Every advertisement for medicines for human use intended for the general public is checked before publication.

checked prior to publication. Radio and television advertisements are provided with a licence after advice from the Commission for the supervision of advertising of medicines for human use or after notification to the FAMHP for the other media.
checked prior to publication. Radio and television advertisements are provided with a licence after advice from the Commission for the supervision of advertising of medicines for human use or after notification to the FAMHP for the other media.

For radio or television advertising, this check is organised by means of a preliminary approval that is granted on the advice of the commission for the supervision of advertising of medicines.
For radio or television advertising, this check is organised by means of a preliminary approval that is granted on the advice of the commission for the supervision of advertising of medicines.

The commission for the supervision of advertising of medicines for human use dealt with 61 approval applications for radio/TV advertising during 16 meetings
The commission for the supervision of advertising of medicines for human use dealt with 61 approval applications for radio/TV advertising during 16 meetings

In spite of there having been no advertising and hardly any information spread about its launch, the Forum was highly successful from the very start: not only did it attract a great number of visitors and messages, but, more importantly, a genuine “support community” was found to emerge as a result of the exchange of views and feelings.
Dès son ouverture, alors qu’aucune publicité ni communication particulière n’avait été faite sur sa création, le forum a rencontré un franc succès: un grand nombre de visiteurs et de messages mais surtout la découverte de la création d’une authentique « communauté de soutien » au travers des réponses échangées.

It is also essential for rational and safe use of medicines that the information in advertising agrees with the elements approved of when the marketing authorisation (MA) for the medicine was granted. Healthcare professionals when making a therapeutic choice should not be influenced by elements that are not associated with the characteristics of the medicine.
It is also essential for rational and safe use of medicines that the information in advertising agrees with the elements approved of when the marketing authorisation (MA) for the medicine was granted. Healthcare professionals when making a therapeutic choice should not be influenced by elements that are not associated with the characteristics of the medicine.

De campagne voor de promotie van het Europese Ecolabel van de federale overheidsdienst Volksgezondheid, Veiligheid van de Voedselketen en Leefmilieu (FOD VVVL) werd op de internationale Internet Advertising Competition (IAC) beloond met maar liefst twee prijzen.
Lors de l’Internet Advertising Competition (concours international de publicité sur Internet), deux prix ont été décernés au Service public fédéral Santé publique, Sécurité de la chaîne alimentaire et Environnement (SPF SPSCAE) pour sa campagne de promotion de l'Ecolabel européen.

Role of independant drug information centers (.PDF) : The case of the Belgian Center for Pharmacotherapeutic Information Robert Vander Stichele - Marc Bogaert Belgisch Centrum voor Farmacotherapeutische Informatie
The role of independant drug information center (.PDF) : The case of the Belgian Center for Pharmacotherapeutic Information Robert Vander Stichele - Marc Bogaert Belgisch Centrum voor Farmacotherapeutische Informatie