Graves asked in HealthAlternative Medicine · 5 months ago

How often is sterilization required during drug development? (USP and EP guidelines etc.)?

for development of injectable drugs, how many sterilization steps does it need to go through in order to comply with the USP and EP guidelines? 

Is a single steam sterilization on the final packaged product enough, or should there be intermediary sterilization steps during the manufacturing process? 

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