Examples of using Study summaries in English and their translations into Slovak
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                        Colloquial
                    
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                        Medicine
                    
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                        Official/political
                    
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                        Programming
                    
And detailed study summaries of the relevant studies. .
This annex is used to present study  references, detailed study summaries and results.
Million study summaries on properties and effects of chemicals;
You will also receive a copy of the robust study summaries from the existing registration.
Study summaries of the information derived from the application of Annexes VII to XI;
The database includes more than two million study summaries on the properties of chemicals and their impact on humans and the environment.
Study summaries of the information derived from the application of Annexes VII to XI;
If not claimed confidential, ECHA will also publish on the substance degree of purity essential for classification and labelling,total tonnage band,(robust) study summaries, information in the safety data sheet and the trade name.
Robust study summaries of the information derived from the application of Annexes VII to XI, if required under Annex I; and.
If the same substance has been registered less than 12 years earlier, ECHA will inform the potential registrant of the names and addresses of previous registrant(s),and of the availability of the relevant study summaries or robust study summaries already submitted to them.
The study summaries or robust study summaries of studies  submitted to support the approval of the active substance;
Potential registrants are remindedthat pursuant to Article 10 of the REACH Regulation, robust study summaries and study summaries made publicly available on the Agency's website may only be used for the purpose of registration where the potential registrant is in legitimate possession of the full study  report or has permission to refer to the full study  report.
The study summaries or robust study summaries of the information referred to in paragraph 1(d) and(e) of this Article;
In the case of a request concerning study summaries or robust study summaries, the Agency shall levy a fee for each study summary  or robust study summary  for which the request is made.
Any study summaries or robust study summaries submitted at least 12 years previously can be freely used for the purposes of registration by another manufacturer or importer.
If a substance has already been registered,a new registrant shall be entitled to refer to the study summaries or robust study summaries, for the same substance submitted earlier, provided that he can show that the substance that he is now registering is the same as the one previously registered, including the degree of purity and the nature of impurities, and that the previous registrant(s) have given permission to refer to the full study  reports for the purpose of registration.
Any study summaries or robust study summaries of studies  submitted in the framework of a registration under this Regulation at least 12 years previously can be used for the purposes of registration by another manufacturer or importer.
Any summaries  or robust study summaries of studies  submitted in the framework of a registration at least 10 years previously may be made freely available by the Agency to any other registrants or potential registrants.
Where a full study  report is available, a study summary shall be submitted;
This means that for each source of information,you need an endpoint study  record containing a study summary or robust study summary.
For that purpose we will use links to Case Studies, Summary Report and additional matirial where appropriate contents are more detailed presented.
The chapters for your thesis generally involve introduction, findings of the research,case studies, summary, and finally the recommendations.
They shall take all reasonable steps to reach an agreement within a deadline set by the Agency as to who is to carry out the test on behalf of the other participants and to submit a summary  orrobust study summary to the Agency.
Study summary: means a summary  of the objectives, methods, results and conclusions of a full study  report providing sufficient information to make an assessment of the relevance of the study; .
The EESC points out that the impact study summary and the impact assessment appended to the proposal under consideration provide no details of the expected repercussions of the new measures on employment and/or working conditions in the sector.
Robust study summary: means a detailed summary  of the objectives, methods, results and conclusions of a full study  report providing sufficient information to make an independent assessment of the study  minimising the need to consult the full study  report;
Always submit the data in the form of a robust study summary.
For hazard information which has not been previously submitted to the Agency,a robust study summary shall be included in the dossier.