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Moreover, ensuring the stability and safety of drug intermediates is paramount. Some intermediates may exhibit toxic properties or be difficult to handle, necessitating careful control of laboratory conditions and adherence to safety protocols. Pharmaceutical companies must continually assess the risk associated with these intermediates, not only for regulatory compliance but also for the safety of their end products.


2. Cost-Effectiveness Coagulation and subsequent filtration processes are often more cost-effective compared to other treatment methods. By facilitating the removal of contaminants at an early stage, these processes reduce the load on subsequent treatment stages, which can be more expensive and energy-intensive.


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Following the successful completion of pilot manufacturing and quality assurance checks, companies move on to full-scale production. This stage involves the extensive use of reactors, filters, and other industrial equipment to produce the API in large quantities. Everything from raw material sourcing to waste management becomes critical to ensuring not only the quality of the APIs but also the safety and compliance with Good Manufacturing Practices (GMP).


 

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