Vertaling van "june 25 " (Nederlands → Frans) :

TERMINOLOGIE

spinocerebellaire ataxie type 25
ataxie spinocérébelleuse type 25

autosomaal recessieve spastische paraplegie type 25
paraplégie spastique autosomique récessive type 25

iriserend insectenvirus 25
virus irisé 25

Yersinia enterocolitica serogroep O:12, 25
Yersinia enterocolitica sérogroupe O:12, 25

humaan rhinovirus 25
rhinovirus humain 25

humaan echovirus 25
échovirus humain de type 25

humaan adenovirus 25
adénovirus humain 25

IN-CONTEXT TRANSLATIONS

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

narcotics and concerning risk limitation and therapeutic advice and of 22 January 1998 governing certain psychotropic substances and concerning risk limitation and therapeutic advice and of 12 April 1974 containing certain provisions relating to substances with hormonal, antihormonal, anabolic, beta-adrenergic, anti-infectious, antiparasitic and anti-inflammatory action Law of 15 July 1985 on the use in animals of substances with hormonal, anti-hormonal, beta-adrenergic or production stimulating action Law of 13 June 1986 on the removal and transplanting of organs, with regard to cells and tissues Law of 28 August 1991 on the practice of veterinary medicine, regarding the provision of medicines to animal carers Law of 5 July 1994 on blood and blood derivatives of human origin Law of 7 May 2004 on experiments on the human person Royal decree of 31 May 1885 approving new instructions for physicians, pharmacists and druggists Royal decree of 22 September 1966 on the conditions and arrangements for the recognition of laboratories for the analysis and checking of medicines Royal decree of 6 June 1960 on the production, preparation and wholesale distribution and delivery of medicines Royal decree no. 78 of 10 November 1967 on the practice of the healthcare professions regarding the dispensing of medicines to the public and Royal decree of 25 September
narcotics and concerning risk limitation and therapeutic advice and of 22 January 1998 governing certain psychotropic substances and concerning risk limitation and therapeutic advice and of 12 April 1974 containing certain provisions relating to substances with hormonal, antihormonal, anabolic, beta-adrenergic, anti-infectious, antiparasitic and anti-inflammatory action Law of 15 July 1985 on the use in animals of substances with hormonal, anti-hormonal, beta-adrenergic or production stimulating action Law of 13 June 1986 on the removal and transplanting of organs, with regard to cells and tissues Law of 28 August 1991 on the practice of veterinary medicine, regarding the provision of medicines to animal carers Law of 5 July 1994 on blood and blood derivatives of human origin Law of 7 May 2004 on experiments on the human person Royal decree of 31 May 1885 approving new instructions for physicians, pharmacists and druggists Royal decree of 22 September 1966 on the conditions and arrangements for the recognition of laboratories for the analysis and checking of medicines Royal decree of 6 June 1960 on the production, preparation and wholesale distribution and delivery of medicines Royal decree no. 78 of 10 November 1967 on the practice of the healthcare professions regarding the dispensing of medicines to the public and Royal decree of 25 September

The number of early phase trials is per capita one of the highest in Europe. Since the publication of the guideline trials for conducting explorative studies in Belgium, in mid June 2007, 25 applications for conducting these clinical trials have been submitted to the FAMHP.
The number of early phase trials is per capita one of the highest in Europe. Since the publication of the guideline trials for conducting explorative studies in Belgium, in mid June 2007, 25 applications for conducting these clinical trials have been submitted to the FAMHP.

Corporate – Issuance of euro bond On June 2, Novartis launched a bond issue of EUR 1.5 billion (approximately USD 2.1 billion) with a coupon of 4.25% under its EUR 15 billion Euro Medium Term Note Programme.
Corporate – émission d’une obligation libellée en euros Le 2 juin, Novartis a lancé l’émission d’une obligation d’EUR 1,5 milliard (environ USD 2,1 milliards) assortie d’un coupon à 4,25% dans le cadre de son programme d’émission de medium term notes (MTN) en euros pour un montant d’EUR 15 milliards.

Ch-basis = RUT 141664 (bridged met RUT Deca 11,25 mg)+ CSP Aug2010 113072 + RtQ Sep2011 + CCSI June 2012 147648
Ch-basis = RUT 141664 bridged met RUT Deca 11,25 mg + CSP Aug2010 113072 + RtQ Sep2011 + CCSI June 2012 147776

Total provisions at June 30, 2010, for the civil and criminal Trileptal investigations and the Five Products investigation amounted to USD 422.5 million, including an addition to the provision in the second quarter of 2010 of USD 25.5 million.
Au 30 juin 2010, le total des provisions pour les investigations civiles et criminelles relatives à Trileptal et aux cinq autres produits s’élevait à USD 422,5 millions, montant qui comprend un supplément d’USD 25,5 millions ajouté au deuxième trimestre 2010 à ces provisions.

The case in the NDTX was transferred to the SDNY and formally consolidated with the actions pending there on June 25, 2010.
Le cas a été transféré du NDTX au SDNY et formellement consolidé le 25 juin 2010 avec les autres plaintes déposées devant ce tribunal.

Poster Abstract P-225 ISBT Madrid; 25 June 2007 [+ update; e-mails van de auteur aan het wetenschappelijke secretariaat van de HGR].
Poster Abstract P-225 ISBT Madrid; 25 June 2007 [+ mise à jour; e-mails de l'auteur au secrétariat scientifique du CSS].

Corporate – Issuance of bond in euros On June 2, Novartis launched a bond issue of EUR 1.5 billion (approximately USD 2.1 billion) with a coupon of 4.25% under its EUR 15 billion Euro Medium Term Note Programme.
Corporate – émission d’un emprunt obligataire en euros Le 2 juin, Novartis a émis un emprunt obligataire d’EUR 1,5 milliard (environ USD 2,1 milliards) assorti d’un coupon à 4,25% dans le cadre de son programme d’émission de medium term notes (MTN) en euros pour un montant d’EUR 15 milliards.

Corporate – Issuance of bond in euros On June 2, Novartis issued a EUR 1.5 billion bond (approximately USD 2.1 billion) with a coupon of 4.25% under its EUR 15 billion Euro Medium Term Note Programme.
Corporate – émission d’un emprunt obligataire en euros Le 2 juin, Novartis a émis un emprunt obligataire d’EUR 1,5 milliard (environ USD 2,1 milliards) assorti d’un coupon à 4,25% dans le cadre de son programme d’émission de medium term notes (MTN) en euros d’un montant d’EUR 15 milliards.