pharmaceutical intermediates manufacturer

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Regulatory agencies, such as the Food and Drug Administration (FDA) and the European Medicines Agency (EMA), require comprehensive stability data as part of the submission process for new drug applications. These entities have established specific guidelines that pharmaceutical companies must follow to ensure that their products meet safety and efficacy standards.


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  • Maintaining the integrity of a gate valve under pressure is critical for ensuring safety and operational efficiency. Regular testing, such as hydrostatic testing, can help verify that valves can withstand their rated pressures without leaking or failing. Additionally, routine inspections should be conducted to check for signs of wear, corrosion, or any other damage that could impact pressure handling capabilities.


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