HRG to present front-end merchandising strategies to the Pharmacy School at Concordia University Wisconsin
WAUKESHA, Wis. — Hamacher Resource Group last week announced co-owner Tom Boyer will present a session about pharmacy layout, design and merchandising principles on Sept. 2 to third-year students in the Pharmacy School at Concordia University Wisconsin. It’s the third year Boyer will present these topics to help students understand the importance and profit potential of the pharmacy front-end. The presentation covers merchandising guidelines to create a shopping experience that improves customer satisfaction and boosts front-of-store sales.
“This is an integral topic within the marketing section of our Pharmacy Management and Leadership class, which is required of all pharmacy students,” stated Dean Arneson, Dean of the School of Pharmacy Science at Concordia. “Students who have attended this special session with Tom in the past have much appreciated his perspective, and we are excited to offer a new group of students a similar opportunity.”
Boyer also has given similar presentations at other pharmacy schools across the country, urging future pharmacists to pay attention to their customers’ needs and design their front-end to encourage a pleasant shopping experience with a healthcare-centric approach.
Acura Pharmaceuticals awarded $300,000 grant to develop Rx abuse deterrent technology
PALATINE, Ill. — Acura Pharmaceuticals last week announced that it has been awarded a $300,000 grant by the National Institute On Drug Abuse of the National Institutes of Health to fund Phase I development of Acura's new, early stage Limitx abuse deterrent technology. The Grant is based on a proposal submitted by the company to advance the development of a self-regulating hydromorphone tablet intended to deter abuse by excess oral consumption of the tablets.
Under the terms of the grant, the company must complete Phase I development by Feb. 28, 2015. Phase I of the project is intended to optimize the formulation in preparation for clinical testing in Phase II.
NIDA funding of Phase II development, for which an application has already been submitted, will be contingent upon assessment by NIDA of the Phase I progress report and determination that the Phase I milestones were achieved, review and approval of other documents necessary for continuation and availability of funds.
Study: High-risk hypertension patients can self-regulate condition
CHICAGO — Among patients with hypertension at high risk of cardiovascular disease, a program where patients measured their blood pressure and adjusted their antihypertensive medication accordingly resulted in lower systolic blood pressure at 12 months compared with patients who received usual care, according to a study in the Aug. 27 issue of JAMA.
Data from national and international surveys suggest that despite improvements over the last decade, significant proportions of patients have poor control of their elevated blood pressure. Self-monitoring of blood pressure with self-titration (adjusting) of antihypertensives results in lower blood pressure in patients with hypertension, but there are no data about patients in high-risk groups, according to background information in the article.
Richard McManus of the University of Oxford and colleagues randomly assigned 552 patients with hypertension and a history of stroke, coronary heart disease, diabetes or chronic kidney disease to either self-monitoring of blood pressure combined with an individualized self-titration algorithm or a control group (i.e., patients received usual care consisting of seeing their healthcare clinician for routine blood-pressure measurement and adjustment of medication, if necessary).
After 12 months, the average systolic blood pressure decreased in both groups, but was lower in the intervention group. Imputation for missing values showed a marginally lower average difference in systolic blood pressure of 8.8 mm Hg. The reduction in diastolic blood pressure also was greater in the self-monitoring group. The results were comparable in all subgroups, without excessive adverse events.
"This trial has shown for the first time, to our knowledge, that a group of high-risk individuals, with hypertension and significant cardiovascular comorbidity, are able to self-monitor and self-titrate antihypertensive treatment following a prespecified algorithm developed with their family physician and that in doing so, they achieved a clinically significant reduction in systolic and diastolic blood pressure without an increase in adverse events," the authors wrote. "This is a population with the most to gain in terms of reducing future cardiovascular events from optimized blood pressure control."
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