WitrynaEuropean Medicines Agency Evaluation of Medicines for Human Use 7 Westferry Circus, Canary Wharf, London E14 4HB, UK Tel. (44-20) 74 18 84 00 Fax (44-20) 74 18 84 16 Witryna26 kwi 2024 · However, the Json returned is. {"book":"It\u0027s a Battlefield"} After some research, I do understand that \u0027 is an apostrophe in Unicode, however, I do not get why it has to be converted to a Unicode as I have seen Json strings that uses ' within a value. I have tried escaping it by adding \ before ' but it did nothing.
Why does Json (obj) convert apostrophe to \u0027?
Witryna25 sty 2010 · Hydrolysis was carried out using 5 ml of 1N HCl per milligram of VAL. The solution was refluxed at 700C for 1 hr. After cooling at room temperature, it was neutralised. The isolation of VALAD as impurity was done by pH partitioning. The oxidative VALO (degradation product of valsartan by oxidation) impurity was also … WitrynaResults: Spiking experiments with individual and complex impurity mixtures show the method can distinguish among samples differing in impurity content by 0.2% wt. The method has been applied to monitor changes in impurity profile among different batches of the same oligonucleotide and changes in the same batch over time (stability analysis). incentives vs subsidies
Determination and validation of valsartan and its degradation …
Witryna15 kwi 2024 · The determinations were performed at a flow rate of 1.0ml/min, and UV detector set at 212 nm. Result and Discussion: The method was found to be specific with relative standard deviation (RSD) less... WitrynaThe pharmaceutical industry is a quality-oriented industry that requires high accuracy while producing drugs and the assay or potency or purity of samples is a key factor to confirm the quality of the drug. The pharmaceutical industry producing life-saving drugs due to that it is important to understand the difference between assay potency and ... WitrynaImpurities can be classified into the following categories: • Organic impurities (process- and drug-related) • Inorganic impurities • Residual solvents Organic impurities can arise during the manufacturing process and/or storage of the new drug substance. They can be identified or unidentified, volatile or non-volatile, and include: ina needle bearing catalog pdf