Process performance qualification protocol
Process performance qualification protocol is a component of process validation: process qualification. This step is vital in maintaining ongoing production quality by recording and having available for review essential conditions, controls, testing, and expected manufacturing outcome of a production process. The Food and Drug Administration recommends the following criteria be included in a PPQ protocol: Manufacturing conditions: Operating parameters, equipment limits, and component inputs What data should be recorded and analyzed What tests should be performed to ensure quality at each production step A sampling plan to outline sampling methods both during and between production batches Analysis methodology that allows for data scientific and risk oriented decision making based on statistical data. Variability limits should be defined and contingencies in the event of non-conforming data established Approval of PPQ protocol from relevant departments Deviations from the standard operation procedures should be made within the framework of the protocol and at the approval of relevant quality control departments. The FDA further recommends a documentation of the protocol be published internally. The report should include: A summation of relevant data and analysis from the protocol An explanation of unexpected data and any other results not mandated by the protocol and its effects on production quality Identify correlating effects and suggest changes to existing processes Conclude if the process performance is adequately qualified to meet performance standards. Should production standards not be met appropriate changes should be outlined
Process performance qualification protocol is a component of process validation: process qualification. This step is vital in maintaining ongoing production quality by recording and having available for review essential conditions, controls, testing, and expected manufacturing outcome of a production process. The Food and Drug Administration recommends the following criteria be included in a PPQ protocol:[1]
- Manufacturing conditions: Operating parameters, equipment limits, and component inputs
- What data should be recorded and analyzed
- What tests should be performed to ensure quality at each production step
- A sampling plan to outline sampling methods both during and between production batches
- Analysis methodology that allows for data scientific and risk oriented decision making based on statistical data. Variability limits should be defined and contingencies in the event of non-conforming data established
- Approval of PPQ protocol from relevant departments
Deviations from the standard operation procedures should be made within the framework of the protocol and at the approval of relevant quality control departments. The FDA further recommends a documentation of the protocol be published internally. The report should include:
- A summation of relevant data and analysis from the protocol
- An explanation of unexpected data and any other results not mandated by the protocol and its effects on production quality
- Identify correlating effects and suggest changes to existing processes
- Conclude if the process performance is adequately qualified to meet performance standards. Should production standards not be met appropriate changes should be outlined
References
[edit]- ^ "Guidance for Industry Process Validation: General Principles and Practices" (PDF). Food and Drug Administration. Archived from the original (PDF) on March 8, 2014. Retrieved 16 December 2014.
External links
[edit]