Examples of using Psurs in English and their translations into German
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Financial
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Ecclesiastic
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Political
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Computer
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Programming
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Official/political
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Political
The marketing authorisation holder should submit 12-monthly PSURs.
These PSURs will address cumulative data on hepatic reactions and NMS.
The Marketing AuthorisationHolder will continue to submit annual PSURs.
No PSURs were submitted as the product is not yet marketed.
The Marketing Authorisation Holder will continue to submit annual PSURs.
PSURs The PSUR submission schedule should follow the PSUR schedule for the reference product.
The CHMP decided that the MAH should continue to submit 6-monthly PSURs.
The MAH will continue to submit yearly PSURs unless otherwise specified by the CHMP.
The CHMP decidedthat the MAH should continue to submit 6 monthly PSURs.
PSURs not sent to the PSUR repository will not fulfil the MAH's legal obligation to submit PSURs.
The MAH will continue to submit yearly PSURs, unless otherwise specified by the CHMP.
Subsequent PSURs will be submitted in accordance to the legislation, unless otherwise specified.
The MAH should continue to submit yearly PSURs, until otherwise specified by the CHMP.
Subsequent PSURs will be submitted in accordance with the European legislation unless otherwise requested by the CHMP.
The marketing authorisation holder will submit PSURs every 6 months unless otherwise specified by the CHMP.
PSURs The PSUR submission schedule for Sildenafil Teva film-coated tablets should follow the PSURs submission schedule for the reference medicinal product.
The MAH will continue to submit yearly PSURs unless otherwise requested by the CHMP.
PSURs The PSUR cycle of Fertavid will correspond to the one attributed to the cross-referred product, Puregon, until otherwise specified.
The PSUR submission schedule forPramipexole Teva tablets should follow PSURs submission schedule for the reference medicinal product.
PSURs The Marketing Authorisation Holder will submit PSURs every six months starting June 2008 until the next renewal application.
The holder of this marketing authorisation holder will submit PSURs every 6 months unless otherwise specified by the CHMP.
From 13 June 2016 all PSURs have to be submitted to the PSUR Repository, an additional PSUR submission to National Competent Authorities is not required anymore.
The EMA does not currently carry out literature searches,and the necessary database for the submission of PSURs is not yet available.
The MAH will continue to submit yearly PSURs for the following three years, unless otherwise specified by the CHMP.
PSURs The PSUR cycle of Glubrava 15 mg/ 850 mg film-coated tablets will correspond to the one attributed to the cross-referenced product, Competact, until otherwise specified.
In particular the number of suspected series adverse drug reactions(ADRs)and periodic safety update reports(PSURs) handled by the EMEA continued to grow in 2000.
Both PSURs for PSUSA-procedures("EU-single assessments") and PSURs for national PSUR submissions("non-EU single assessments") have to be uploaded in the PSUR repository.
Adverse reaction reporting would be simplified, resulting in fewer,more relevant periodic safety updated reports(PSURs) being prepared by firms which are marketing authorisation holders.
PSURs The Marketing Authorisation Holder will submit 6 monthly PSURs for one year after the Commission Decision on the extension application for alli 60 mg hard capsules then yearly for 2 years and every three years thereafter.
The Marketing Authorisation Holder will submit PSURs every six months for a period of two years after the Commission Decision on the extension of the indication to treat symptomatic mild to moderately severe dementia in patients with idiopathic Parkinson' s disease, then yearly for two years and then every three years thereafter.