Exemple de utilizare a Draft assessment report în Engleză și traducerile lor în Română
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Draft assessment report.
RMS prepares a draft assessment report;
The draft assessment report is sent to the applicant through R4BP 3.
The evaluating competent authority finalises the draft assessment report and the conclusions of its evaluation.
(5) The draft assessment report has been reviewed by the Member States and the Commission within the Standing Committee on Plant Health.
Spain acting asnominated rapporteur Member State, submitted a draft assessment report concerning the substance to the Commission 30 November 1998.
(e) the draft assessment report, except the elements thereof which have been accepted as confidential in accordance with Article 14 of the Directive.
It shall make it available to the public, after giving the applicant two weeks to request, pursuant to Article 60,that certain parts of the draft assessment report be kept confidential.
EFSA opinion on draft assessment reports and ECHA classification of active substances.
The Republic of Finland evaluated malathion and,without having requested Cheminova A/S to submit further scientific data to it, forwarded its draft assessment report to EFSA on 2 February 2004 with a view to peer review.
The format of the draft assessment report shall be established in accordance with the procedure referred to in Article 76(2).
The United Kingdom acting asnominated rapporteur Member State, submitted a draft assessment report concerning the substance to the Commission on 15 October 1998.
The draft assessment report shall be submitted in the format recommended in accordance with the procedure provided for in Article 19 of the Directive.
For an application for authorisation of a plant protection product containing an active substance not yet approved,Member States shall start the evaluation as soon as it has received the draft assessment report referred to in Article 12(1).
(e) the draft assessment report, except the elements thereof which have been accepted as confidential in accordance with Article 14 of Directive 91/414/EEC.
Whereas concern in terms of transparency and conflicts of interest has furthermore been raised by several stakeholders over the fact that the RMS given responsibility by the Commission for the renewal of an assessment report may be the same one which did the initial draft assessment report;
The draft assessment report shall be submitted in the format recommended in accordance with the procedure provided for in Article 19 of Directive 91/414/EEC.
Within twelve months of the date of the notification provided for in the first subparagraph of Article 9(3), the rapporteur Member State shall prepare andsubmit to the Authority a report(hereafter called“draft assessment report”) assessing whether the active substance can be expected to meet the requirements of Article 4.
The Authority shall circulate the draft assessment report received from the rapporteur Member State to the applicant, the other Member States and the Commission.
The final draft assessment report and, if the draft assessment report is positive the draft summary of product characteristics, are sent to the applicant and to the concerned MSCAs through R4BP 3.
After receiving the updated summary dossier and the draft assessment report referred to in paragraph 1, the EFSA shall, within 30 days, acknowledge receipt of the report to the rapporteur Member State.
This draft assessment report- which recommended the inclusion of malathion in Annex I to the Directive whilst limiting its use to ornamentals in greenhouses- was the subject of peer review by the Member States and EFSA.
The nominated rapporteur Member States, submitted draft assessment reports concerning the substances to the Commission on 17 December 1998(acibenzolar-s-methyl), 11 February 1998(cyclanilide), 30 July 1999(ferric phosphate), 28 May 1998(pymethrozine) and 8 July 1999(pyraflufen-ethyl), respectively.
In exceptional cases where the draft assessment report clearly does not fulfil the requirements concerning the format recommended by the Commission, the Commission shall agree with the EFSA and the rapporteur Member State on a period for resubmission of an amended report. .
EFSA had to evaluate the rapporteur Member State's draft assessment report and deliver its opinion on whether the active substance could be expected to meet the safety requirements of the Directive to the Commission one year after receipt of the draft assessment report at the latest.
The EFSA shall evaluate the rapporteur's draft assessment report and deliver its opinion on whether the active substance can be expected to meet the safety requirements of Directive 91/414/EEC to the Commission at the latest one year after receipt of the rapporteur Member State draft assessment report.
In exceptional cases where the draft assessment report clearly does not fulfil the requirements concerning the format recommended by the Commission, the Commission shall agree with the EFSA and the rapporteur Member State on a period for resubmission of an amended report. .