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fda
fda
Dernière mise à jour : 2020-06-15
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food and drug administration (fda)
Dernière mise à jour : 2020-10-20
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the fda has approved a test that uses isothermal nucleic acid amplification technology instead of pcr.
inaprubahan ng fda ang pagsusuri na gumagamit ng isothermal nucleic acid amplification technology sa halip na pcr.
Dernière mise à jour : 2024-04-15
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on 21 march 2020, cepheid similarly received eua from the fda for a test that takes about 45 minutes.
noong marso 21, 2020, ang cepheid ay nakatanggap din ng eua mula sa fda para sa pagsusuri na tumagal nang 45 minuto.
Dernière mise à jour : 2020-08-25
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n95 respirators are approved for industrial settings but the fda has authorised the masks for use under an emergency use authorisation (eua).
ang mga n95 respirator ay inaprubahan para sa mga lugar pang-industriya subalit ang fda ay nagpahintulot na gamitin ang mga maskarang iyon sa ilalim ng emergency use authorisation (eua).
Dernière mise à jour : 2020-08-25
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e cigarettes also are controversial because of various regulatory issues. for example, in 2008 the u.s. food and drug administration (fda) concluded that e cigarettes were unapproved drug delivery devices, and the following year, invoking its authority to regulate drugs and drug delivery devices under the federal food, drug, and cosmetic act (ffdca, fdca, or fd
kontrobersyal din ang e cigarette dahil sa iba 't ibang isyu sa regulasyon. halimbawa, sa 2008 us food and drug administration (fda) concluded na e sigarilyo ay hindi naaprubahan aparato paghahatid ng bawal na gamot, at sa susunod na taon, invoking kanyang kapangyarihan upang pangalagaan gamot at mga aparato paghahatid ng bawal na gamot sa ilalim ng federal food, drug, at cosmetic act (ffdca, fdca, o fd
Dernière mise à jour : 2022-06-06
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