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How the Rise in US Pharmacy Deserts Impacts Patients’ Health

Drug Topics

The 3 experts provided detailed insights into the prominence of pharmacy deserts, issues within its definitions, how they impact both patients and pharmacists, and how they are an inherently community-based issue.

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Independent Pharmacists’ Unique Role During Disaster Management Efforts

Drug Topics

Aside from properly preparing medications during a disaster, Phillips mentioned the importance of establishing communication with patients. There definitely can be a lot of communication barriers throughout disaster preparedness, but again, in this day and age, there are a lot more routes of communication that occur during those times.

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The future of clinical pharmacy in Europe with ESCP president Monika Lutters

Hospital Pharmacy Europe

In 2022, the International Journal of Clinical Pharmacy published a position paper on the definition of clinical pharmacy and its relationship to pharmaceutical care. The revised definition highlights that clinical pharmacy is both a professional practice and an area of research. This is a huge problem.

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MetrioPharm gains orphan drug status from EMA for MP1032

Pharmaceutical Technology

MetrioPharm’s lead compound, MP1032, has received orphan drug designation (ODD) from the European Medicines Agency (EMA) for treating Duchenne muscular dystrophy (DMD) in children. July 30, 2025 Share Copy Link Share on X Share on Linkedin Share on Facebook MP1032 is intended for treating Duchenne muscular dystrophy.

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HS market forecast to reach $7.8bn across 7MM by 2034

Pharmaceutical Technology

compound annual growth rate (CAGR) is largely attributed to the launch of novel biologics and small molecules targeting multiple inflammatory pathways beyond TNF-alpha inhibition. CAGR is largely attributed to the launch of novel biologics and small molecules. Give your business an edge with our leading industry insights.

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FDA Posts Slate of Seven Warning Letters Following Company Inspections

PharmTech

While FDA warning letters generally do not authorize the execution of any definitive actions by the agency, they do specify actions that may be taken if FDA’s suggestions and requests are not adhered to, usually to be communicated by a company within a window of 15 business days of receipt of FDA’s letter.

FDA
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Efficacy and Safety in CPX-351 vs 7+3 in Adults Younger Than 60 Years With AML-MRC or t-AML

Pharmacy Times

Definition of major bleeding in clinical investigations of antihemostatic medicinal products in non-surgical patients. 2022;140(12):1345-1377. doi:10.1182/ blood.2022016867 J Thromb Haemost. 2005;3(4):692-694. doi:10.1111/j.1538- 1538- 7836.2005.01204.