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During this phase, the process is made and documented in detail. The significant process parameters as well as corresponding running ranges are recognized.Offer a concise summary of the final results acquired through the validation or verification routines. Spotlight important conclusions, deviations, and successes observed throughout the process.
• The frequency of sampling and screening must be decreased in this period soon after productive completion of period I&II.In the event the residue obtained is down below the satisfactory level, and medically Harmless and it don’t effect on product quality, similar quantity of residue can be recognized.4. Any big transform in the process equi
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