
- Did you mean
- limitations
Search results - 8 results
Characterisation and Hazard identification of substandard and Falsified Antimicrobial Drugs. The CantiBio project 2016-2020
the amount of drug released is under the limit at the time point described by the USP. In addition to that, low equivalences of dissolution profiles between SF antimicrobials and genuine products were ...
Clustering of Tadalafil API Samples According to their Manufacturer in the Context of API Falsification Detection
can be limited to the test distinguishing that manufacturer. Health Topics: Illegal medicines Médicaments illégaux Illegale geneesmiddelen Service: Médicaments et produits de santé Geneesmiddelen en ...
Relative response factors and multiple regression models in liquid chromatography to quantify low-dosed components using alternative standards-proof of concept: total Δ9-THC content in cannabis flowers using CBD as reference.
have limited shelf-life properties. Also, in herbal matrices, multiple compounds could be necessary to be quantified, needing a whole series of different (related) reference standards. In these cases, ...
OMCL testing and the API working group: Part of the solution?
manufacturers. Despite the efforts, API testing within the network is limited, compared to the surveillance of finished products. Though it has to be said that the risk for quality deficiencies and falsification ...
Use of near infrared spectroscopy and chemometrics for the classification of different Cannabis spp. samples found in Belgium
concentration of 0.2 % (m/m) [2]. However, there are only limited cannabis seizures because it is difficult to discriminate between legal CBD flowers and cannabis flowers with a Δ9- THC concentration higher than ...
GEONs API fingerprint project: Selection of analytical techniques for clustering of sildenafil citrate API samples
and research on provenance and identity will be required. Of course, if the suspected sample claims to originate from one of the manufacturers included in the study, analysis can be limited to the test ...
Comparative dissolution study on substandard and falsified antibiotics encountered in Belgium
Agency for Medicines and Health Products (FAMHP), were subjected to dissolution studies. The results indicated that 9 out of 19 illegal samples failed to meet the dissolution limits prescribed by the ...
Impurity profiling of the most frequently encountered falsified polypeptide drugs on the Belgian market
class one elemental impurities arsenic (As) and lead (Pb). One sample was contaminated with Pb while multiple samples were found with concentrations up to ten times the ICH toxicity limit for parenteral ...