Examples of using Documentation submitted in English and their translations into Finnish
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Medicine
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Official
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Colloquial
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Financial
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Ecclesiastic
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Official/political
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Computer
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Programming
The Commission shall examine documentation submitted by Member States.
Documentation submitted to the Commission pursuant to Article 5 of Regulation 438/2001 should be revised.
The applicant may refer to other documentation submitted alone or with a simplified IMPD.
Based on the documentation submitted by the MAH and the scientific discussion within the Committee, the CHMP considered that the benefit/ risk ratio of neurontin and associated names is favourable relating to.
Marketing Authorisation Holders have been assessed based on the documentation submitted and the scientific discussion within the Committee.
Based on the documentation submitted and the scientific discussion within the Committee, the.
The manualofproceduresfor monitoring programmes now provides for tighter checks on the documentation submitted by Member States concerning national selection procedures points 1.4 and 2.
Based on the documentation submitted by the Marketing Authorisation Holder and the scientific discussion within the Committee.
Authorisation Holders has been assessed based on the documentation submitted and the scientific discussion within the Committee.
Documentation submitted, the scientific discussion within the Committee and the new wording proposed in the updated Guideline on SPC dated October 2005 and the latest QRD template.
Authorisation Holders has been assessed based on the documentation submitted and the scientific discussion within the Committee.
Based on the documentation submitted by the MAH and the scientific discussion within the Committee, the CPMP considered that the benefit/ risk ratio of Prograf and associated names is favourable for use relating to.
Authorisation Holders have been assessed based on the documentation submitted and the scientific discussion within the Committee.
Shall check that the documentation submitted in support of the application complies with Articles 12 to 13d and ascertain whether the conditions for the issue of the marketing authorisation have been fulfilled;
The competent authority or the Agency to which the application has been submitted in accordance with Article 6 shall inform the applicant if the documentation submitted in support of the application is insufficient.
Been assessed based on the documentation submitted and the scientific discussion within the Committee.
Cooperation in Allied Signal/Honeywellwas greatly facilitated by the fact that the merging parties hadgranted full waivers allowing for the exchange of market data and other documentation submitted to thetwo authorities.
For this purpose the Commission shall examine documentation submitted by Member States and shall conduct the audits necessary to evaluate the system.
The scope of the referral was the harmonisation of the Summaries of Products Characteristics,• the Summary of Products Characteristic proposed by the Marketing Authorisation Holders has been assessed based on the documentation submitted and the scientific discussion within the Committee.
Only information and documentation submitted before the interview to determine which state is responsible for examining their application is taken into account.
The technical regulation shall be listed in the Compendium of Candidates if supported by an affirmative vote in accordance with paragraph 7.1 of Article 7 of Annex B. The documentation submitted with the request for that regulation shall be appended to the listed technical regulation.
On the one hand, the quality control of the EIA documentation submitted by the developer could be improved. On the other hand, the quality of the EIA process itself could be reinforced.
The scope of the referral was to discuss the benefit/ risk of glucosamine hydrochloride in the proposed indication The Summary of Products Characteristic, labelling andpackage leaflet proposed by the applicant has been assessed based on the documentation submitted and the scientific discussion within the Committee.
Benefit/ Risk considerations Based on the documentation submitted by the MAH and the scientific discussion within the Committee, the CPMP considered that the benefit/ risk ratio of Lopid is favourable for use relating to.
Certification confirming acceptance of the provisions made by the railway undertaking to meet specific requirements necessary for the safe operation on therelevant network concerning the application of TSI and national safety rules and the certification of staff and rolling stock, based on documentation submitted by the railway undertaking as described in Annex IV.
Based on the documentation submitted by the MAH and the scientific discussion within the Committee, the CHMP considered that the benefit/risk ratio of STAMARIL and associated names is favourable for use relating to.
In order to facilitate the functioning of the authorisation and mutual recognition procedures, it is appropriate to establish a system for the mutual exchange of information and Member States, the Commission andthe Agency should make available to each other on request the particulars and scientific documentation submitted in connection with applications for authorisation of biocidal products.
The documentation submitted with this application consists of literature referring to the use of the originator product Eqvalan, a comparative pharmacokinetic study using Equimectin and Eqvalan, and a supplementary clinical field study.
The Summary of Products Characteristic proposed by the applicant has been assessed based on the documentation submitted and the scientific discussion within the Committee. the CHMP has recommended the granting of the Marketing Authorisations with amendments of the Summary of Product Characteristics as set out in Annex III for Lansoprazol HEXAL and associated names see Annex I.
Based on the documentation submitted by the Marketing Authorisation Holders and the scientific discussion within the Committee, the CPMP considered that the benefit/ risk ratio of calcium folinate(solution for injection and powder for solution for injection) is positive for the agreed and harmonised indications.