Pharmaceutical Impurity Reference Standards

All of Veeprho's products go through multiple quality checks to ensure that every product we ship is of the highest quality.

Our multiple quality checks have made our products rejection rate of less than 0.01%, which is the lowest among all our competitors.

Specific information about impurities is found in current pharmacopoeias like RRT RRF, which helps the client make a judgement to purchase impurities manufacture by Veeprho.

Veeprho's impurities are analysed by respective monograph to match RRT and RRF mentioned in table format in the monograph, it indicates compliance of USP, EP, BP and other pharmacopoeias, additional scientific data like MASS, NMR, IR, are support to respective impurities' structure.

Veeprho impurity reference standards are well characterised and been used for quantitative analysis purpose in QC and Analytical.

We at Veeprho understand your urgency and work around the clock to ensure all our in-stock products are ready to dispatch on the next working day after your order is received.

In case of high urgency, we recommend you contact us via email or by the "Request a Quotation" button. This will allow us to understand your requirement and timeline effectively and to support you appropriately.

All our ready to dispatch products are pre-inspected by our Quality Control (QC) and Analytical Team.