Sentence examples for good practice guidelines on from inspiring English sources

We call for a review of existing S&T networks for DRR and the development of good practice guidelines on S&T networks for DRR.

The trial is being conducted in accordance with the ethical principles in the Declaration of Helsinki and good practice guidelines on the proper conduct of research.

In accordance with the ethical responsibilities placed on researchers using animals, there are published good practice guidelines on the total number and frequency of injections that can be administered to an animal (Diehl et al., 2001).

Policies restricting the societal costs of physician emigration from developing countries such as good practice guidelines and taxes on host countries have not yet produced their expected effect or in some cases have not been established at all.

The General Medical Council (GMC), in its "Good Practice Guidelines" (2013), gives clear guidelines on the prescribing of ULM [ 22].

Estimation of carbon stocks present in biomass is based either on IPCC (Good Practice guidelines (IPCC, GPG, 2003) or published literature for conversion and other factors starting from the growing stock (GS) data of forest inventories.

These problems can be avoided with the expanded use of workflow-based tools and performance metrics, which are critical to ensuring downstream quality and improving risk management, both central themes of the recently released Good Practice Guideline (GCP) by the International Conference on Harmonization (ICH-GCP E6 R2)).

The list of VAP prevention measures we used as a reference for good practices guidelines [ 10] could be criticized on several grounds, e.g. it does not include subglottic secretions drainage [ 26].

Both NordiNet® IOS and ANSWER Program® are guided by the Good Pharmacoepidemiological Practice guidelines on the design and reporting of observational studies, as defined by the International Society for Pharmacoepidemiology, and the STrengthening the Reporting of OBservational studies in Epidemiology (STROBE) guidelines.

Study personnel were trained on ICH-GCP (International Conference on Harmonization - Good Clinical Practice) guidelines and on informed consent procedures as part of a professional development program.

For example, a 2001 FDA report notes that clinical trial "sponsors have raised concerns regarding the capacity of the institutional review boards in some of the emerging sites to adequately review research according to Good Clinical Practice Guidelines, under the International Conference on Harmonization or FDA standards" [2].