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Once the API has passed QC and QA checks, it must be submitted for regulatory approval. This involves compiling extensive documentation demonstrating that the API is safe, effective, and manufactured according to the highest standards. Regulatory agencies, such as the U.S. Food and Drug Administration (FDA) or the European Medicines Agency (EMA), review this information before granting approval for the API to be used in drug formulations.


One of the most notable applications of sodium thiocyanate is its role as a reagent in chemical synthesis. It is frequently utilized in organic chemistry for the preparation of thiocyanate derivatives, which are essential in producing various organic compounds. The nucleophilic properties of thiocyanate make it an effective agent in substitution reactions, where it can replace halides in organic molecules. This property is valuable in synthesizing agrochemicals and pharmaceuticals, where specific functional groups are necessary to impart desired biological activities.


The global API market is characterized by its robust growth trajectory, fueled by a combination of aging populations, growing awareness of health issues, and advances in drug development. As pharmaceutical companies continue to emphasize innovation and sustainability, the demand for high-quality APIs is at an all-time high. Moreover, the COVID-19 pandemic has amplified the need for a secure and reliable supply chain for APIs, underscoring their critical role in drug production.


Isoflurane An Overview of Its Use in Anesthesia


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The Potential Benefits of Pyrroloquinoline Quinone Disodium Salt (PQQ)


When diluted to a 1% solution, ethanediol diacetate retains its solvent properties while minimizing some of the concentrated effects that might occur at higher concentrations. This dilution makes it particularly useful in applications where a subtle solvent action is necessary without overwhelming effects on other components.


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