Sentence examples for guidelines in respect of from inspiring English sources

There may be large differences between guidelines in respect of the literature available to review: the size of the relevant economics literature, its relevance, its quality, its timeliness, its generalisability.

The Mental Welfare Commission for Scotland has, as part of its remit, a responsibility to develop good practice guidelines in respect of medical treatment in the setting of mental disorders.

Student/VU In this focus group study, we interviewed users of communication guidelines in order to explore facilitating and impeding characteristics of guidelines in respect of the actual utilisation of these guidelines.

Even so, certified and uncertified breast centres tend to differ in respect of guideline-concordant treatment, also referred to as guideline compliance.

While targeting the volcanic islands of the eastern Caribbean, the source-book and its content are largely generic, and the advice and guidelines contained therein have equal validity in respect of improving communication before and during crises at any volcano, and have application to the communication issue in respect of a range of other geophysical hazards.

The guidelines for information provision differed between the UK and the Netherlands and Denmark in respect of the 'right not to know' [ 36, 23, 43].

A few previous papers describing how GPs deal with multimorbidity reported briefly on the value of medical guidelines in this respect.

UKIP put huge emphasis on local issues and Mr Wilson was unwilling to follow UKIP guidelines in this respect".

In the case that struck down the sentencing guidelines in the state of Washington, Justice Anthony M. Kennedy objected in dissent that the court was failing to give the states proper respect for their legislative choices on criminal justice.

In every respect, of course, but one.

In vivo data are also being used to develop more clinically relevant laboratory and computer models for preclinical testing of medical devices as a basis for improving international standards of testing of these devices, and informing regulatory agencies (such as the FDA in the USA, or EU directives governing CE marking) in establishing guidelines with respect to the safety of new medical devices.