Akshay Kadam16 Jan, 2023Health
Based on type, pharmaceutical intermediates are divided into GMP segment and non-GMP segment. GMP products are manufactured in a controlled atmosphere according to the prescribed quality standards b, in accordance with the quality standards stipulated by international organizations. Major risks include unexpected product expectations that can lead to adverse health effects, and failure to follow packaging guidelines. Non-GMP practices have been employed for preclinical and toxicology studies to assess technical feasibility and formulations and further scale up to clinical and commercial production.
 
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