Traduction de «Normes toxicopharmacologiques » (Français → Anglais) :

pharmaco-toxicological protocols/standards

industrial toxico-vigilance

environmental standard [ environmental quality standard | standard relating to the environment | environmental quality(UNBIS) ]

look clean, smart and tidy | maintain personal hygienic standards | maintain personal hygiene standards | maintain personal standards of hygiene

ensure compliance with health, safety, and hygiene standards | manage standards of health and safety | manage health and safety certification | manage health and safety standards

Goodenough norms

Committee on Standards and Technical Regulations | Committee on technical standards and regulations | Standards and Technical Regulations Committee

coverage of quality standards applicable to aquaculture products | scope of quality standards applicable to aquaculture products | quality standards applicable to aquaculture products | scope of quality systems applicable to aquaculture products

biological standard

Whereas the Commission should be empowered to adopt, in close cooperation with the Committee for the Adaptation to Technical Progress of the Directives on the Removal of Technical Barriers to Trade in Medicinal Products, any necessary changes in the requirements for the testing of proprietary medicinal products set out in the Annex to Council Directive 75/318/EEC of 20 May 1975 on the approximation of the laws of the Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of proprietary medicinal products (1), as last amended by Directive 87/19/EEC (2), to take account o ...[+++]f the special nature of medicinal products derived from human blood or human plasma so as to ensure a higher level of quality, safety and efficacy,

2. to describe their findings in accordance with Council Directive 81/852/EEC of 28 September 1981 on the approximation of the laws of the Member States relating to analytical, pharmaco-toxicologial and clinical standards and protocols in respect of the testing of veterinary medicinal products (1), and in particular to state: (a) in the case of analysts, whether the product conforms with the stated composition, providing any reasons for the control testing methods which the manufacturer is to use;

(b) to describe their observations in accordance with Council Directive 75/318/EEC (1) of 20 May 1975, on the approximation of the laws of the Member States relating to analytical, pharmacotoxicological and clinical standards and protocols in respect of the testing of proprietary medicinal products, and to state, in particular: - in the case of the analyst, whether the product is consistent with the declared composition, giving any substantiation of the control methods employed by the manufacturer;