Bisoprolol EP Impurity E is an impurity that can occur in Bisoprolol formulations due to synthesis or storage conditions.

Regulatory bodies require monitoring impurities like Bisoprolol EP Impurity E to ensure the safety and efficacy of Bisoprolol formulations.

It forms as a by-product under conditions such as heat, moisture, or pH changes during synthesis or storage.

By maintaining optimal storage conditions, controlling pH, and conducting routine quality checks, the formation of this impurity can be managed.

Detection methods include GC-MS, LC-MS, and HPLC-MS for precise impurity profiling and analysis.

Chemicea provides COA, H-NMR, MASS, HPLC, and TGA reports, with additional reports like CNMR, IR, UV, DEPT, Water content, and CHNS available on request.

Yes, Chemicea’s documents meet the standards of major regulatory agencies such as the USFDA, EMA, ANVISA, TGA, and PMDA.

It is stable for shipping at room temperature. Specific storage conditions are outlined in the Certificate of Analysis (COA).

Yes, Chemicea offers both standard and customized pack sizes to meet client needs.

Chemicea provides Bisoprolol EP Impurity E as a reference standard to support regulatory compliance, method validation, and impurity profiling.