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PHARMACEUTICAL MANUFACTURING HANDBOOK
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Handbook Of Pharmaceutical Manufacturing Formulations
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20 Regulatory Definition Of “Lot” 21 CFR 210.3 Lot - A Batch, Or A Specific Identified Portion Of A Batch, Having Uniform Character And Quality Within Specified Limits; Or, In The Case Of A Drug Product Produced By Continuous Process, It Is A Specific Identified Amount Produced In A Unit Of Time Or Quantity In A Manner Tha 1th, 2024

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