Tuesday 18 November 2014

Simvastatin Impurity

We would like inform you that Veeprho Pharmaceuticals s.r.o. is a qualified vendor for certified impurity reference standards. We are manufacturer and supplier of Simvastatin impurities like to Simvastatin Impurity A, Simvastatin Impurity B, Simvastatin Impurity C, Simvastatin Impurity D (Dimer Impurity), Simvastatin Impurity F, Simvastatin Impurity G which are isolated by preparative HPLC and Lyophillized. It is acceptable to all regulatory agencies in the world like US-FDA, MHRA, MCC, WHO, Brazil and Japan. These Simvastatin impurities are also used for ANDA filling, DMF filling and genotoxic study.

We are manufacturer and supplier of

  • Certified impurity of Simvastatin.
  • All Simvastatin impurity which are used for ANDA filing/DMF filing.
  • All Simvastatin USP, EP, BP pharmacopoeia impurity.
  • All Simvastatin Impurity as per pharmacopoeia RRT.
  • All Simvastatin Impurity with characterization data along with certificate of analysis (COA).
  • Unknown impurity of Simvastatin with structure elucidation with help of C NMR, H NMR, MASS, CHN, HPLC data.
  • Isolation of unknown impurity of Simvastatin.

We understand the importance of RRT, RF, POTENCY of impurity and most of your vendors do not understand this critical information. We are recognized for quality material manufacturer, quality documentation and quality service. We deliver material on time as per our commitment with you, we know the value of your time and we understand that your project time line depends on availability of impurity standards.

Write to us on the venkat@veeprhopharma.com email id to get specific quote.







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