Application of statistical process control for spotting compliance to good pharmaceutical practice
ABSTRACT For the release of pharmaceutical products into the drug market; most of the pharmaceutical companies depend on acceptance criteria - that are set internally, regulatory and/or pharmacopeially. However, statistical process control monitoring is underestimated in most quality control in case...
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2018-07-01
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doaj-043adff4f12046e897e8ff10c1aa24652020-11-25T00:53:40ZengUniversidade de São PauloBrazilian Journal of Pharmaceutical Sciences2175-97902018-07-0154210.1590/s2175-97902018000217499S1984-82502018000200301Application of statistical process control for spotting compliance to good pharmaceutical practiceMostafa Essam EissaAhmedy Mahson AbidABSTRACT For the release of pharmaceutical products into the drug market; most of the pharmaceutical companies depend on acceptance criteria - that are set internally, regulatory and/or pharmacopeially. However, statistical process control monitoring is underestimated in most quality control in cases; although it is important not only for process stability and efficiency assessment but also for compliance with all appropriate pharmaceutical practices such as good manufacturing practice and good laboratory practice, known collectively as GXP. The current work aims to investigate two tablet inspection characteristics monitored during in-process control viz. tablet average weight and hardness. Both properties were assessed during the compression phase of the tablet and before the coating stage. Data gathering was performed by the Quality Assurance Team and processed by Commercial Statistical Software packages. Screening of collected results of 31 batches of an antibacterial tablet - based on Fluoroquinolone -showed that all the tested lots met the release specifications, although the process mean has been unstable which could be strongly evident in the variable control chart. Accordingly, the two inspected processes were not in the state of control and require strong actions to correct for the non-compliance to GXP. What is not controlled cannot be predicted in the future and thus the capability analysis would be of no value except to show the process capability retrospectively only. Setting the rules for the application of Statistical Process Control (SPC) should be mandated by Regulatory Agencies.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502018000200301&lng=en&tlng=enStatistical process control (SPC)In-process controlGXPFilm coated tabletFluoroquinoloneCapability analysisPharmaceutical practice. |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mostafa Essam Eissa Ahmedy Mahson Abid |
spellingShingle |
Mostafa Essam Eissa Ahmedy Mahson Abid Application of statistical process control for spotting compliance to good pharmaceutical practice Brazilian Journal of Pharmaceutical Sciences Statistical process control (SPC) In-process control GXP Film coated tablet Fluoroquinolone Capability analysis Pharmaceutical practice. |
author_facet |
Mostafa Essam Eissa Ahmedy Mahson Abid |
author_sort |
Mostafa Essam Eissa |
title |
Application of statistical process control for spotting compliance to good pharmaceutical practice |
title_short |
Application of statistical process control for spotting compliance to good pharmaceutical practice |
title_full |
Application of statistical process control for spotting compliance to good pharmaceutical practice |
title_fullStr |
Application of statistical process control for spotting compliance to good pharmaceutical practice |
title_full_unstemmed |
Application of statistical process control for spotting compliance to good pharmaceutical practice |
title_sort |
application of statistical process control for spotting compliance to good pharmaceutical practice |
publisher |
Universidade de São Paulo |
series |
Brazilian Journal of Pharmaceutical Sciences |
issn |
2175-9790 |
publishDate |
2018-07-01 |
description |
ABSTRACT For the release of pharmaceutical products into the drug market; most of the pharmaceutical companies depend on acceptance criteria - that are set internally, regulatory and/or pharmacopeially. However, statistical process control monitoring is underestimated in most quality control in cases; although it is important not only for process stability and efficiency assessment but also for compliance with all appropriate pharmaceutical practices such as good manufacturing practice and good laboratory practice, known collectively as GXP. The current work aims to investigate two tablet inspection characteristics monitored during in-process control viz. tablet average weight and hardness. Both properties were assessed during the compression phase of the tablet and before the coating stage. Data gathering was performed by the Quality Assurance Team and processed by Commercial Statistical Software packages. Screening of collected results of 31 batches of an antibacterial tablet - based on Fluoroquinolone -showed that all the tested lots met the release specifications, although the process mean has been unstable which could be strongly evident in the variable control chart. Accordingly, the two inspected processes were not in the state of control and require strong actions to correct for the non-compliance to GXP. What is not controlled cannot be predicted in the future and thus the capability analysis would be of no value except to show the process capability retrospectively only. Setting the rules for the application of Statistical Process Control (SPC) should be mandated by Regulatory Agencies. |
topic |
Statistical process control (SPC) In-process control GXP Film coated tablet Fluoroquinolone Capability analysis Pharmaceutical practice. |
url |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502018000200301&lng=en&tlng=en |
work_keys_str_mv |
AT mostafaessameissa applicationofstatisticalprocesscontrolforspottingcompliancetogoodpharmaceuticalpractice AT ahmedymahsonabid applicationofstatisticalprocesscontrolforspottingcompliancetogoodpharmaceuticalpractice |
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