Sentence examples for reasonable medicine from inspiring English sources

Pharmacy financial data is available in remote settings and can be used towards determination of "reasonable" medicine price goals.

Health services research is needed to develop sustainable and "reasonable" medicine price goals and strategic initiatives to reach them.

In so doing, we provide the first example of how cost accounting methods can be applied to pharmacy financial data to ascertain "reasonable" medicine price and mark-ups.

This study demonstrates the utility of analyzing financial data obtained from pharmacies to predict costs of establishing new pharmacy businesses and determine reasonable medicine prices and mark-ups that are affordable but still ensure pharmacy viability.

In the Hamilton case, Lloyd argued a storefront is necessary to give medical cannabis patients reasonable access to medicine.

In the context of Pharmaceutical Management Agency's (PHARMAC's) fixed budget for procuring and subsidising medicines, there was reasonable satisfaction with the range of medicines available rare disorder medicines being the clear exception.

The Clinton Foundation announced Thursday that it had brokered an agreement among several drug makers that it hoped would ensure a steady supply of a crucial malaria medicine at reasonable prices for the world's poor.

Trying to get more people from poor backgrounds into the top professions is a reasonable endeavour: the army, medicine, the law, politics, media and most professions are dominated by the privately educated.

The rejection of the conventional cancer treatment by the followers of traditional herbal medicine is reasonable due to the fact known by humans and every animal species: each plant and juice that could be consumed is safe.

This problem highly impairs the practice of medicine with reasonable skill and safety to patients because of their illness or dependence on drugs [ 3- 5].

In response, the FDA revised its rules in 2009 to include specific criteria and requirements that must be met to authorize access, such as that the potential risks of the experimental medicine are reasonable in the context of the patient's disease (U.S. Food and Drug Administration, 2009; Expanded Access to Investigational Drugs for Treatment Use, 74 Federal Register 40900-40945).