Search results - 10 results

Evaluation of a point-of-care test for the diagnosis of Taenia solium neurocysticercosis in rural southern Tanzania: a diagnostic accuracy study.

UI 37-51) and the antigen ELISA (50%, 43-56). For the subset of neurocysticercosis cases with at least one active (ie, vesicular) lesion, sensitivity was above 98% for the TS POC test, the rT24H- ETIB, ...

Spectroscopic approaches for conformity analysis of e-liquids

Though, vaping is not without health concerns. The long-term effects  are still not fully understood, and there have been reports of health problems associated with e-cigarette use, including lung damage. ...

Chemical and toxciological characterization of e-liquid cigarettes

electronic cigarette (e-cigarette) has increased significantly in the past decade. In Belgium, the implementation of the revised European Tobacco Products Directive (TPD) in 2014 marked a turning point for ...

Characterization and hazard identification of substandard and falsified antimicrobials encountered in Belgium

together with anti-malarials, one of the most popular medicines that have been encountered as illegal substandard and falsified (SF) medical products. It has been demonstrated that SF products of these ...

Identification of Flavouring Substances of Genotoxic Concern Present in E-Cigarette Refills

alert for genotoxicity in at least one of the two (Q) SAR models. For these substances, genotoxicity data was collected from previous European safety evaluations in different regulatory domains (e.g. by ...

Analysis of illegal peptide drugs via HILIC-DAD-MS.

p.562-571 (2017) Abstract: Biopharmaceuticals have established themselves as highly efficient medicines, and are still one of the fastest growing parts of the health-product industry. Unfortunately, the ...

Advanced Methods for Dose and Regimen Finding During Drug Development: Summary of the EMA/EFPIA Workshop on Dose Finding (London 4-5 December 2014).

I Skottheim Rusten Source: CPT Pharmacometrics Syst Pharmacol, Volume 6, Issue 7, p.418-429 (2017) Abstract: Inadequate dose selection for confirmatory trials is currently still one of the most challenging ...

Detection and risk evaluation of counterfeit medicines based on physico-chemical properties: the fingerprint and chemometrics approach

physico-chemical properties risk evaluation Abstract: Counterfeit medicines pose a global threat to public health; both developing and industrialized countries are exposed to pharmaceutical forgery. These products ...

General considerations on the biosafety of virus-derived vectors used in gene therapy and vaccination.

one of the requirements within the European regulatory framework covering the conduct of clinical trials using GMO. Risk assessment methodologies for the environmental risk assessment of genetically ...

Non-sterile pharmaceutical water: source of life and/or potential carrier for opportunistic pathogens

world. Evidently, this molecule is also one of the major resources utilized by the pharmaceutical industry. Water can be present as an excipient or might be used for reconstitution of products, during ...

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