Mar 2, 2020 15:47
4 yrs ago
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Russian term
Оформление результатов исследований
Russian to English
Medical
Medical (general)
documents
Оформление результатов Исследований
6.1 На основании анализа документации и проведенных Исследований оформляют заключение/протокол.
6.2 В заключении/протоколе должны содержаться следующие сведения:
- информация об организации, проводящей Исследования (полное наименование, адрес, телефон и др.);
http://docs.cntd.ru/document/1200140578
6.1 На основании анализа документации и проведенных Исследований оформляют заключение/протокол.
6.2 В заключении/протоколе должны содержаться следующие сведения:
- информация об организации, проводящей Исследования (полное наименование, адрес, телефон и др.);
http://docs.cntd.ru/document/1200140578
Proposed translations
(English)
4 +2 | см. | Marlin31 |
5 | presentation of test results | Viktoria Kantemyr |
4 | Documenting examination results | Pavel Altukhov |
3 | Completion of test results | Igor Arefyev |
Proposed translations
+2
26 mins
Selected
см.
preparation of the study/trial/research report
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Note added at 37 mins (2020-03-02 16:24:32 GMT)
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http://www.fao.org/3/s4862e/s4862e04.htm
3. PREPARATION OF THE STUDY REPORT
https://onlinelibrary.wiley.com/doi/10.1002/9781118873922.ch...
This chapter provides guidance for managing the beginning and the end of a nonclinical study, including the development and management of the study protocol and data interpretation and reporting after the study.
https://www.triga-s.de/en/project-management/
PROJECT MANAGEMENT
Documentation:
Study Protocol development according to the regulatory requirements / DIN 14155 and DIN 13612
Preparation of investigator contracts
Creation of Case Report Forms (CRFs, eCRF) and Patient Information / Declarations of Consent
Compilation of documentation, application and submission to the responsible ethics commissions and authorities
Implementation and preparation of publications
Documentation of the clinical data and preparation of the study report according to GCP / ICH
Documentation of the laboratory values according to GCP and GCLP
--------------------------------------------------
Note added at 37 mins (2020-03-02 16:24:32 GMT)
--------------------------------------------------
http://www.fao.org/3/s4862e/s4862e04.htm
3. PREPARATION OF THE STUDY REPORT
https://onlinelibrary.wiley.com/doi/10.1002/9781118873922.ch...
This chapter provides guidance for managing the beginning and the end of a nonclinical study, including the development and management of the study protocol and data interpretation and reporting after the study.
https://www.triga-s.de/en/project-management/
PROJECT MANAGEMENT
Documentation:
Study Protocol development according to the regulatory requirements / DIN 14155 and DIN 13612
Preparation of investigator contracts
Creation of Case Report Forms (CRFs, eCRF) and Patient Information / Declarations of Consent
Compilation of documentation, application and submission to the responsible ethics commissions and authorities
Implementation and preparation of publications
Documentation of the clinical data and preparation of the study report according to GCP / ICH
Documentation of the laboratory values according to GCP and GCLP
4 KudoZ points awarded for this answer.
Comment: "Thank you!"
17 mins
Completion of test results
-
24 mins
presentation of test results
or
Test Results Presentation
Test Results Presentation
36 mins
Documenting examination results
http
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