Comprehensive Data Review Records for Pharmaceutical Processes
This template is designed for documenting the review of logged data from pharmaceutical manufacturing and testing processes.
It provides a record of the periodic review of key data points such as temperature, humidity, pressure, and time to ensure compliance
with regulatory standards and internal
protocols.
| Parameter | Details |
|---|---|
| Review Title | Data Review Record for [Process or Equipment Name] |
| Data Reviewed |
 – Humidity – Pressure – Time – Other critical parameters |
| Reviewer | [Name and designation of the person responsible for data review] |
| Date of Review | [Date of review] |
| Comments/Observations | [Any observations or deviations noted during the review process] |
| Compliance Status | [Indicate whether the data is compliant with regulatory standards] |
| Action Taken | [If any corrective actions were required, specify the actions taken] |
| Signatories | QA, QC, Reviewer |