Glossary entry (derived from question below)
Spanish term or phrase:
así lo ameriten
English translation:
[if warranted] on grounds of public health
Spanish term
así lo ameriten
En caso de incumplimiento de las obligaciones previstas en los artículos precedentes, esta
Administración Nacional podrá suspender la importación y/o comercialización de los productos descriptos en el
Artículo 1° de la presente disposición elaborados con destino a la República Argentina en los establecimientos
antes mencionados cuando consideraciones de salud pública así lo ameriten.
mi intento en base a la información que encontré: when public health considerations so warrant.
gracias
Mar 27, 2022 01:12: Juan Gil changed "Language pair" from "English to Spanish" to "Spanish to English"
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Proposed translations
[if warranted] on grounds of public health
The following English example is taken from the EU website, with what I assume to be its Spanish translation. I could see an original Spanish drafter using a phrase like "cuando las consideraciones de salud pública así lo ameriten" rather than "por razones de salud pública," which doesn't sound very natural to me in Spanish.
"This recommendation serves to facilitate the implemention [sic] of existing provisions related to restrictions of the freedom of movement on grounds of public health
La presente Recomendación tiene por objeto facilitar la aplicación de las disposiciones existentes relativas a las restricciones de la libertad de circulación por razones de salud pública."
https://eur-lex.europa.eu/legal-content/EN-ES/TXT/?fromTab=A...
agree |
Jennifer Levey
: You're right - 'if warranted' is part and parcel of 'on grounds of' and is best omitted.
8 hrs
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Thanks, Jennifer.
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agree |
patinba
11 hrs
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Thanks, Pat.
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agree |
Yvonne Gallagher
18 hrs
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Thanks, Yvonne.
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agree |
neilmac
1 day 4 hrs
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agree |
abe(L)solano
2 days 4 hrs
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agree |
AllegroTrans
2 days 14 hrs
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if (it is) justified by public health considerations/on justified grounds relating to public health
The consumer and successive purchasers are entitled to a legal warranty affording protection against any types of defects or faults. The whole supply chain is jointly and severally liable for granting and complying with a legal warranty. All manufacturers, distributors, producers and retailers are considered suppliers. A supplier is any individual or legal entity, public or private, that carries on in a professional manner, even occasionally, production activities, assembling, creation, construction, transformation, importation, trade mark concession, distribution and commercialisation of goods and services to consumers.
In case of non-compliance with the obligations set forth in the preceding articles, the National Administration may suspend the import and/or marketing of the products described in Article 1 of this provision in the establishments mentioned above if (it is) justified by public health considerations.
on justified grounds relating/related to public health considerations
on public health grounds
With the exception of those medicinal products which are subject to the centralized Community authorization procedure established by Council Regulation (EEC) No 2309/93 of 22 July 1993 laying down Community procedures for the authorization and supervision of medicinal products for human and veterinary use and
establishing a European Agency for the Evaluation of Medicinal Products (1) a marketing authorization for a medicinal product granted by a competent authority in one Member State ought to be recognized by the competent authorities of the other Member States unless there are serious grounds for supposing that the authorization of the medicinal product concerned may present a risk to public health.
The competent authority may, in exceptional circumstances and on public health grounds grant exemptions from paragraphs 4 and 5. Such exemptions must be duly justified.
https://ec.europa.eu/health/system/files/2016-11/dir_2001_83...
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Note added at 33 perc (2022-03-26 23:15:30 GMT)
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ARTÍCULO 1°.- Los laboratorios titulares de certificados de especialidades medicinales inscriptas en el Registro de Especialidades Medicinales (REM) y comercializadas, que contengan, como monodroga, alguno de los Ingredientes Farmacéuticos Activos (IFA) mencionados a continuación, deberán presentar los protocolos para la realización de los estudios de equivalencia in vivo dentro de los ciento veinte (120) días corridos contados a partir de la entrada en vigencia de la presente disposición.
Vencido dicho plazo, sin mediar la presentación de los protocolos esta Administración Nacional podrá proceder, sin intimación previa, a la suspensión de la comercialización de las especialidades medicinales involucradas cuando consideraciones de salud pública así lo ameriten.
https://www.argentina.gob.ar/normativa/nacional/disposición-...
ARTICLE 1: Laboratories holding certificates for medicinal products registered in the Register of Medicinal Products (REM) and marketed, which contain, as monodrugs, any of the Active Pharmaceutical Ingredients (API) listed below, shall submit the protocols for the performance of in vivo equivalence studies within one hundred and twenty (120) calendar days as from the entry into force of this provision.
Upon expiry of such term, without the submission of the protocols, the National Administration may suspend without prior notice the marketing authorization of the medicinal products involved if the(ir) authorization may present a risk to public health.
Thank you! |
agree |
Muriel Vasconcellos
3 hrs
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Thank you very much. Warm hugs from Budapest.
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agree |
ormiston
14 hrs
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Thank you very much.
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[when public health] affairs so dictate
Thank you!! |
whenever may be so justified
Community funds, and that appropriate corrective measures are taken whenever justified by considerations of costs and benefits
Thank you! |
Reference comments
comment
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Note added at 10 hrs (2022-03-27 09:40:07 GMT)
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In fact it is better than all those suggested!
Thank you so much Liz!!!! |
Discussion