The vast physiological differences between species treated in veterinary medicine coupled with differences within species create the necessity for a widely diverse array of dosing options. Historically, this need has not, and in reality, cannot be metby the drug manufacturing community. This leads to...
In this clip, Jeffrey Lombardo, PharmD, who is the executive patient safety officer for University at Buffalo's patient safety organization Empire State Patient Safety Assurance Network, explains the challenges pharmacists will face in transitioning to USP800. In...
Following this year’s Match Day on March 15, pharmacists at US Pharmacopeia (USP) explain some of the opportunities student pharmacists can pursue outside of the traditional pharmacy career model.
Non-adherence is also of concern as DOACs have short half-lives and missed doses could decrease efficacy, increasing the risk of thromboembolic events. Other factors such as poly-pharmacy, cognitive impairment, hospitalisation, history of bleeding and/or falls are common in the elderly, which coul...
G. Alternative Radiochemical Purity Testing Procedures for the Compounded Radiopharmaceuticals Approved from 1988; APhA: Washington, DC, 1998.Search in Google Scholar 30. Mahoney, WD, McGough, GC, The American Pharmaceutical Association – Academy of Pharmacy Practice and Management (APhA-APPM). ...
Photo © Museu de Arte Contemporânea da USP Collection, São Paulo, Brazil. Photo Romulo Fialdini These compositions engage me on two levels. On the first level the elements compose a narrative, conjure a visual place. The narrative is structured to point a parallel second level of ...
tumor-promoting features still stands. we found that ZNF655, a TF, can affect a variety of functions in a variety of cancers. For example, Chen et al., indicated that ZNF655 promotes the progression of glioma through transcriptional regulation of AURKA [33]. Teng et al., demonstrated that...
Tegretol® (Carbamazepine USP): Prescribing Information; U.S. Food and Drug Administration: Silver Spring, MD, USA, 2007. [Google Scholar] U.S. Department of Health and Human Services; Food and Drug Administration; Center for Drug Evaluation and Research. Guidance for Industry Estimating the ...
Therefore, the obtained results showed that the tested plant raw material was of high microbiological quality and suitable for further technological processing. According to the EP and WHO, this raw material can be used without the addition of boiling water. However, the requirements of the USP ...
"Pharmacy is an exact science and cannot be compared to the fast moving consumer goods sector, and therefore access to markets has to be specialised and optimal at all stages of the supply chain. The inspections at the borders are punitive," he adds. Recent investment of over US$40 million...