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instrumentalities

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The Collaborative International Dictionary of English v.0.48 (gcide)

Instrumentality \In`stru*men*tal"i*ty\, n.; pl.
{Instrumentalities}.
The quality or condition of being instrumental; that which is
instrumental; anything used as a means; medium; agency.
[1913 Webster]

The instrumentality of faith in justification. --Bp.
Burnet.
[1913 Webster]

The discovery of gunpowder developed the science of
attack and defense in a new instrumentality. --J. H.
Newman.
[1913 Webster]

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instrumentalities	查看　instrumentalities　在Google字典中的解释	Google英翻中〔查看〕
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Clinical trials - Regulation EU No 536 2014
The Regulation ensures a greater level of harmonisation of the rules for conducting clinical trials throughout the EU It introduces an authorisation procedure based on a single submission via a single EU portal, an assessment procedure leading to a single decision, rules on the protection of subjects and informed consent, and transparency
REGULATION (EU) No 536 •2014 OF THE EUROPEAN PARLIAMENT AND OF THE . . .
REGUL ATION (EU) No 536 2014 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 16 Apr il 2014 on clinical tr ials on medicinal products for human use, and repealing Directive 2001 20 EC (Text with EEA relevance) THE EUROPEAN PARLIAMENT AND THE COUNCIL OF THE EUROPEAN UNION,
Updated document - Questions Answers : Clinical Trials Regulation (EU . . .
Updated document - Questions Answers : Clinical Trials Regulation (EU) No 536 2014 ; News announcement; 29 September 2023; Directorate-General for Health and Food Safety; 1 min read; Updated document - Questions Answers : Clinical Trials Regulation (EU) No 536 2014 15 JANUARY 2025; regulation5362014_qa_en pdf
CLINICAL TRIALS REGULATION (EU) NO 536 2014 - Public Health
Clinical Trials Regulation (EU) No 536 2014 with a view to facilitating its implementation This documents sets out frequently-asked 'questions and answers' regarding the implementation of the rules on clinical trials
March 2024, version 05 - Public Health
This is a quick guide on the main rules and procedures of the Clinical Trials Regulation (EU) No 536 2014 (CTR) [1] for sponsors who wish to conduct clinical trials (national and multinational) in the European Union (EU) European Economic Area (EEA) or have ongoing clinical trials in this region
EudraLex - Volume 10 - European Commission - Public Health
Regulation (EU) No 536 2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001 20 EC
Brussels, 8. 12. 2017 C(2017) 8179 final - Public Health
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Questions and Answers Document – Regulation (EU) 536 2014 – Version 6. 9 . . .
Questions and Answers Document – Regulation (EU) 536 2014 – Version 6 9, July 2024 15 JANUARY 2025; regulation5362014_qa_en pdf English (1 68 MB - PDF) Download Details Publication date 28 August 2024 Author Directorate-General for Health and Food Safety Share this page Public Health
Summaries of Clinical Trial Results for Laypersons - Public Health
The EU Clinical Trials Regulation 536 2014 (Article 37) (EU CT Regulation) requires sponsors to provide summary results of clinical trials in a format understandable to laypersons These layperson summaries will be made available in a new EU database once it becomes available and is approved according to the timelines set forth in the Regulation
Ethical considerations for clinical trials on medicinal products . . .
1 Regulation (EU) No 536 2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001 20 EC (Text with EEA relevance)

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