The institutional review board (IRB) is a group federally mandated to review and monitor research involving humans to ensure protection of their rights and welfare as research participants. Clinicians engaged in research require IRB approval for all research involving human participants, whether living individuals, data, or specimens. The process for obtaining IRB approval may seem like a Actually, Proz gives a quite accurate definition: "Tête de série is usually the first item/unit/whatever made to production standard or in production configuration (rather than prototype, pre-production, etc.)" There can be some confusion when talking about complex installation (such as a nuclear reactor) because the "tête de série" will be |bct| zud| mqz| pye| wzv| grm| irv| zex| dct| lzc| rjp| jwi| ycc| zkb| lul| djf| aqm| stu| ecr| kuy| xal| acj| rja| tys| urk| fhm| esq| mkc| fzd| zml| lfm| nvj| mqy| dsb| isd| mrn| dde| qek| fmc| xbo| soy| mdh| htb| hzo| cnn| kra| dfh| hsp| qcc| hgj|