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This document serves as a quality control record sheet for the VGKC Ab Kit, detailing various lot numbers, expiry dates, assay results, and quality control procedures. It includes information on control samples, assay dates, and decay factors related to the product\'s usage.
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How to fill out quality control record sheet

01
Start by gathering all necessary information about the product or process being recorded.
02
Clearly label the record sheet with the date and the specific quality control process.
03
List the items being checked, including specifications or standards to be met.
04
During inspection, mark the findings on the sheet using appropriate codes (e.g., pass, fail, out of tolerance).
05
Record any discrepancies or issues found, providing detailed notes if necessary.
06
Assign a responsible person to perform the quality check and sign the record.
07
Ensure all data is reviewed and verified before finalizing the record sheet.
08
Store the completed record sheet in a designated location for future reference.

Who needs quality control record sheet?

01
Quality control teams
02
Manufacturing supervisors
03
Compliance officers
04
Product managers
05
Audit teams
06
Anyone involved in the quality assurance process
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A quality control record sheet is a document used to record and monitor the quality of products or processes in order to ensure compliance with specified standards.
Typically, manufacturers, service providers, or any organization involved in quality management are required to file a quality control record sheet.
To fill out a quality control record sheet, enter the date, the specific quality control metrics being measured, the results of those measurements, and any corrective actions taken if necessary.
The purpose of a quality control record sheet is to provide a systematic approach to documenting quality checks and ensuring that standards are met consistently over time.
Information that must be reported includes the date of inspection, the type of product or process, quality metrics, results of tests, and any follow-up actions required.
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