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method description and comprehensive in-house validation".
method description and comprehensive in-house validation.

method description and comprehensive in-house validation".
method description and comprehensive in-house validation.

til e-mailadressen: rea-urf-validation@ec.europa.eu.
to the functional mailbox: rea-urf-validation@ec.europa.eu.

titel på dokumentet process validation limitations to the use of ethylene oxide in the manufacture of medicinal products
limitations to the use of ethylene oxide in the manufacture of medicinal products

ellison og r. wood, harmonized guidelines for single-laboratory validation of methods of analysis.
ellison, and r. wood, harmonized guidelines for single-laboratory validation of methods of analysis.

validation of the episkin skin irritation test — 42 hours assay for the prediction of acute skin irritation of chemicals.
validation of the episkin skin irritation test — 42 hours assay for the prediction of acute skin irritation of chemicals.

a national validation study of the acute-tosic- class method — an alternative to the ld50 test.
a national validation study of the acute-toxic- class method — an alternative to the ld50 test.

& liebsch, m. (1998), the ecvam international validation study on in vitro tests for skin corrosivity.
& liebsch, m. (1998), the ecvam international validation study on in vitro tests for skin corrosivity.

det samme gælder laboratoriedyr, hvorimod velfærdsaspekterne for dyr til videnskabelige formål vurderes af european centre for the validation of alternative methods (ecvam).
the same also applies to laboratory animals, whereby the welfare of animals used for scientific purposes is handled by the european centre for the validation of alternative methods (ecvam).

2 chamberlain, m. and basketter, d.a. (1996) the local lymph node assay: status of validation.
chamberlain, m. and basketter, d.a., (1996) the local lymph node assay: status of validation.

stability testing of existing active substances and related finished products summary of requirements for active substances process validation (update) quality aspects of veterinary medicinal products administered via drinking water
stability testing of existing activesubstances and related finished productssummary of requirements for active substancesprocess validation (update)quality aspects of veterinary medicinal products administered via drinking water

this applies in particular to the members of deutsche bundesbank , banque de france , banca d' italia and banco de españa , if the t2s programme board decides on the validation of the 4cb deliveries ,
this applies in particular to the members of deutsche bundesbank , banque de france , banca d' italia and banco de españa , if the t2s programme board decides on the validation of the 4cb deliveries ,

iccvam (interagency coordinating committee on the validation of alternative methods). (1997). validation and regulatory acceptance of toxicological test methods.
iccvam (interagency coordinating committee on the validation of alternative methods)., (1997) validation and regulatory acceptance of toxicological test methods.

der er på kommissionens websted offentliggjort en vejledning om metodevalidering og kvalitetskontrolprocedurer for analyse af pesticidrester i fødevarer og foder (»method validation and quality control procedures for pesticide residue analysis in food and feed«) [5].
guidance concerning ‘method validation and quality control procedures for pesticide residue analysis in food and feed’ is published on the commission website [5].