Sentence examples for implementation of a requirement from inspiring English sources

Negative verification demonstrates that no flaws exist in a particular implementation of a requirement.

This paper proposes an implementation of a requirement management process that is based on the aforementioned reformulation of the design process.

In this case then, the implementation of a requirement of informed consent will not be inconsistent with satisfying other principles such as beneficence and justice.

If there are individual health benefits and reduced waste of resources to be gained from only partial access to the patient's personal medication information, then the implementation of a requirement of informed consent resulting in a limited registration of information or limited access to use the registered information, will not pose a hindrance to the improvement of health care.

The question remains, however, if the satisfaction of the principles of beneficence and justice in the case of the Shared Medicine Profile are inconsistent with respecting and protecting personal autonomy through the implementation of a requirement of informed consent, i.e. if we are here faced with a true dilemma.

Several respondents indicated that while they supported continued access to an intervention, they had reservations about the practical implementation of such a requirement: "…if you're going to say … these benefits have to keep going after the research I think there's going to be a lot of research …that will stop because of the money issue".

Here, a prototypical implementation of all requirements serves as the basis for an evaluation.

If those procedures are not being followed, or if the judge was "not still convinced... that there will be no voter disenfranchisement arising out of the Commonwealth's implementation of a voter identification requirement for purposes of the upcoming election" then he would be "obliged to enter a preliminary injunction," the higher court wrote.

It will also play a role in the implementation of the requirement for industry to submit data they already hold on use of their medicines in children.

Larger health warnings were required by the national law since 2005; however, the law granted a long gray period for the implementation of the requirement; the packs with 4% warnings became outlawed only in February 2008.

The implementation of each requirement would be dependent on the implementation of another requirement.