INVESTIGATION REPORT FOR HARDNESS FAILURE DURING IN-PROCESS CHECK AT COMPRESSION STAGE IN AMLODIPINE 10 MG TABLETS

INVESTIGATION REPORT

Hardness Failure During In-Process Check at Compression Stage

1. Objective

To investigate and identify the root cause for the failure in tablet hardness observed during the in-process check at the compression stage for Amlodipine Tablet 10 mg, Batch No. PGH/T/25-002 on 21/07/25, and to recommend suitable corrective and preventive actions (CAPA) to prevent recurrence.

Key Parameter of Below Page:

Hardness Failure During In-Process Check at Compression Stage

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Click the link to download word file copy of this document:
https://pharmaguidehub.com/product/investigation-report-for-hardness-failure-during-in-process-check-at-compression-stage-in-amlodipine-10-mg-tablets/

Key Parameter of Below Page:

Hardness Failure During In-Process Check at Compression Stage

Find below pages for complete report

Key Parameter of Below Page:

Hardness Failure During In-Process Check at Compression Stage

Find below pages for complete report

Key Parameter of Below Page:

Hardness Failure During In-Process Check at Compression Stage

Find below pages for complete report

Key Parameter of Below Page:

Hardness Failure During In-Process Check at Compression Stage

Find below pages for complete report

Key Parameter of Below Page:

Hardness Failure During In-Process Check at Compression Stage

Find below pages for complete report

Click the link to download word file copy of this document:
https://pharmaguidehub.com/product/investigation-report-for-hardness-failure-during-in-process-check-at-compression-stage-in-amlodipine-10-mg-tablets/

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