Примери за използване на Reliability and robustness на Английски и техните преводи на Български
{-}
-
Colloquial
-
Official
-
Medicine
-
Ecclesiastic
-
Ecclesiastic
-
Computer
High reliability and robustness- long life time(20 years).
The set of tips-in resistant, plugs, angles, martini and handles with key give reliability and robustness in closing windows.
High power, reliability and robustness make Hielscher's ultrasonicators the“work horse” in soybase production.
(c) considerations as regards subject safety and data reliability and robustness submitted under paragraph 4 or 6 of Article 18.
This increases reliability and robustness compared to a monolithic doors which has only a couple of track connections for the whole panel.
With countless installations worldwide,Hielscher's ultrasonic extractors are well recognized for their high extraction rate, reliability and robustness.
The reliability and robustness of Hielscher ultrasonicators make sure that you can process your materials with high efficiency getting the desired outcome.
Welding Column&Boom Manipulators of Wuxi Success stands out not only for innovation in design and quality of manufacture,but also for reliability and robustness.
Besides high ultrasonic output, reliability and robustness, Hielscher Ultrasonics' industrial ultrasonic processors can be precisely controlled and monitored.
Observations 48 85 Such variations between the national and Commission figures raise questions regarding the reliability and robustness of the calculation methodologies used.
(d) the reliability and robustness of the data generated in the clinical investigation, taking account of statistical approaches, design of the investigation and methodological aspects, including sample size, comparator and endpoints;
One of the key strengths of all Iveco vehicles has always been the reliability and robustness of their frames, and these strengths are even more evident on the new New Trakker.
The use of formal methods for software and hardware design is motivated by the expectation that, as in other engineering disciplines,performing appropriate mathematical analysis can contribute to the reliability and robustness of a design.
The reliability and robustness of the data generated in the clinical investigation, taking account of statistical approaches, design of the investigation and methodological aspects, including sample size, comparator and endpoints;
Such delegation shall be without prejudice to the responsibility of the sponsor,in particular regarding the safety of subjects and the reliability and robustness of the data generated in the clinical trial.
The information which is to appear on the primary and secondary packaging shall ensure subject safety and reliability and robustness of the data generated in the clinical trial, while taking account of the design of the clinical trial, whether the products are investigational or auxiliary medicinal product, and whether they are products with particular characteristics.
The products referred to in the first paragraph shallbe labelled appropriately in order to ensure the safety of the subject and the reliability and robustness of data generated in the clinical trial.
They shall be stored, returned and/or destroyed as appropriate and proportionate to ensure the safety of the subject and the reliability and robustness of the data generated in the clinical trial, in particular, taking into account whether the IMP is an authorised IMP, and whether the clinical trial is a low-intervention clinical trial.
For the purposes of this Article, a‘serious breach' means a breach likely to affect to a significant degree the safety and rights of a subject or the reliability and robustness of the data generated in the clinical trial.".
Notwithstanding point(b) of paragraph 1, where the specific circumstances, provided for in the protocol, of a clinical trial so require in order toensure the safety of the subject or the reliability and robustness of data generated in a clinical trial, additional particulars relating to the identification of the clinical trial and of the contact person shall appear on the outer packaging and the immediate packaging of authorised investigational medicinal products.
Where the clinical trial referred to in paragraph 4 has been conducted outside the Union, it shall have been conducted in accordance with principles equivalent to those of this Regulation as regards the rights and safety of the subject and the reliability and robustness of the data generated in the clinical trial.
(d) a clear description of the consequences of the substantial modification as regards the rights and safety of the subject and the reliability and robustness of the data generated in the clinical trial.
The particulars listed in sections A, B and C, other than those particulars listed in paragraph 9, may be omitted from the label of a product and made available by other means, for example by use of a centralised electronic randomisation system, use of a centralised information system,provided that the safety of the subject and the reliability and robustness of data are not compromised.
The principal investigator shall assign tasks among the members of the team of investigators in a way which is not compromising the safety of subjects and the reliability and robustness of the data generated in the clinical trial at that clinical trial site.
The Regulation defines a substantial amendment as“any change to any aspect of the clinical trial which is made after notification of the decision referred to in Articles 8, 14, 19, 20 and 23 and which is likely to have a substantial impact on the safety orrights of the subjects or on the reliability and robustness of the data generated in the clinical trial.”.
Member States shall make the processes set out in paragraph 5 subject to appropriate and proportionate requirements to ensure subject safety and reliability and robustness of the data generated in the clinical trial.
The Commission shall be empowered to adopt delegated acts in accordance with Article 89 in respect ofamending Annex VI in order to ensure subject safety and the reliability and robustness of data generated in a clinical trial or to take account of technical progress.
Investigational medicinal products shall be manufactured by applying manufacturing practice which ensures the quality ofsuch medicinal products in order to safeguard the safety of the subject and the reliability and robustness of clinical data generated in the clinical trial(‘good manufacturing practice').
The Commission shall be empowered to adopt delegated acts in accordance with Article 89 in order to specify the principles and guidelines of good manufacturing practice and the detailed arrangements for inspection for ensuring the quality of investigational medicinal products,taking account of subject safety or data reliability and robustness, technical progressand global regulatory developments in which the Union or the Member States are involved.