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The pharmaceutical intermediate market is subject to stringent regulatory oversight. Regulatory agencies, such as the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA), impose strict guidelines to ensure the safety and efficacy of pharmaceutical products. Manufacturers must adhere to Good Manufacturing Practices (GMP) and other regulations to ensure that intermediates meet quality standards.


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- Safety Compliance Many industries are subject to safety regulations regarding static electricity. Using anti-static additives can help manufacturers meet these standards and reduce the risk of hazardous incidents.


The Manufacturing Process


Understanding Fillers in Polymers Enhancing Performance and Cost-Effectiveness


How to Incorporate PQQ into Your Routine


Chlorination involves adding chlorine (Cl2), sodium hypochlorite (NaOCl), or calcium hypochlorite (Ca(OCl)2) to water. When chlorine is introduced, it undergoes hydrolysis to form hypochlorous acid (HOCl) and hydrochloric acid (HCl) in water. Hypochlorous acid is the active disinfecting agent responsible for killing bacteria, viruses, and other microorganisms


The Need for Folic Acid Production


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