Traduction de «determining the conditions under which » (Néerlandais → Français) :

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

Non-IFRS disclosures Net debt/liquidity and free cash flow are non-IFRS financial measures, which means they should not be interpreted as measures determined under IFRS.
Informations non-IFRS Les dettes/liquidités nettes et le free cash flow sont des grandeurs financières qui ne relèvent pas des normes IFRS, ce qui signifie qu’elles ne sauraient être interprétées comme ayant été déterminées par lesdites normes.

Non-IFRS disclosures Net debt and free cash flow are non-IFRS financial measures, which means they should not be interpreted as measures determined under IFRS.
Informations non-IFRS Les dettes nettes et le free cash-flow sont des grandeurs financières qui ne relèvent pas des normes IFRS, ce qui signifie qu’elles ne sauraient être interprétées comme ayant été déterminées par lesdites normes.

Non-IFRS disclosures Net liquidity/debt and free cash flow are non-IFRS financial measures, which means they should not be interpreted as measures determined under IFRS.
Informations non-IFRS Les liquidités/dettes nettes et le free cash-flow sont des grandeurs financières qui ne relèvent pas des normes IFRS, ce qui signifie qu’elles ne sauraient être interprétées comme ayant été déterminées par lesdites normes.

Export certificates Manufacturing sites under FAMHP supervision have to be able to provide documents quickly which demonstrate that the GMP conditions are being complied with.
Export certificates Manufacturing sites under FAMHP supervision have to be able to provide documents quickly which demonstrate that the GMP conditions are being complied with.