Examples of using Reference dates in English and their translations into Greek
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Colloquial
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Official
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Medicine
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Ecclesiastic
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Financial
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Official/political
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Computer
The marketing authorisation holder shall submit the first periodic safety update report for this product with the requirements set out in the list of Union reference dates(EURD list)
The requirements for submission of periodic safety update report for this medicinal product are set out in the list of Union reference dates(EURD list)
The requirements for submission of periodic safety update reports for this medicinal product are set out in the list of Union reference dates(EURD list)
The requirements for submission of periodic safety update reports for this medicinal product are set out in the list of Union reference dates(EURD list)
The marketing authorisation holder shall submit PSURs for this product in accordance with the requirements set out in the list of Union reference dates(EURD list) provided for under Article 107c(7)
The marketing authorisation holder shall submit periodic safety update reports for this product in accordance with the requirements set out in the list of Union reference dates(EURD list)
The marketing authorisation holder shall submit the first periodic safety update report for this product with the requirements set out in the list of Union reference dates(EURD list)
The requirements for submission of periodic safety update report for this medicinal product are set out in the list of Union reference dates(EURD list) provided for under Article 107c(7)
The requirements for submission of periodic safety update reports for this medicinal product are set out in the list of Union reference dates(EURD list)
The requirements for submission of periodic safety update reports for this medicinal product are set out in the list of Union reference dates(EURD list) provided for under Article 107c(7)
Periodic Safety Update Reports The marketing authorisation holder shall submit periodic safety update reports for this product in accordance with the requirements set out in the list of Union reference dates(EURD list)
The requirements for submission of periodic safety update reports including liver reports for this medicinal product are set out in the list of Union reference dates(EURD list)
Xiapex Leflunomide teva The requirements for submission of periodic safety update reports for this medicinal product are set out in the list of Union reference dates(EURD list)
The requirements for submission of PSURs for this medicinal product are set out in the list of Union reference dates(EURD list)
The requirements for submission of periodic safety update reports for this medicinal product are set out in the list of Union reference dates(EURD list)
The marketing authorisation holder shall submit PSUR for this product in accordance with the requirements set out in the list of Union reference dates(EURD list)
The requirements for submission of periodic safety update reports for this medicinal product are set out in the list of Union reference dates(EURD list) provided for under Article 107c(7)
The requirements for submission of periodic safety update reports for this medicinal product are set out in the list of Union reference dates(EURD list)
The marketing authorisation holder shall submit periodic safety update reports for this product in accordance with the requirements set out in the list of Union reference dates(EURD list)
The marketing authorisation holder shall submit periodic safety update reports for this product in accordance with the requirements set out in the list of Union reference dates(EURD list) provided for under Article 107c(7)