Development and Validation of the Production Process of Parecoxib Sodium Freeze-dried Preparation Based on Quality by Design / 中国药学杂志
Chinese Pharmaceutical Journal
;
(24): 1337-1341, 2017.
Article
in Chinese
| WPRIM
| ID: wpr-858626
ABSTRACT
OBJECTIVE:
To prepare parecoxib sodium freeze-dried preparation, evaluate and validate the feasibility of the production process and quality reliability of the preparation.METHODS:
Risk assessment of the production process of parecoxib sodium freeze-dried preparation was performed based on the method of quality by design (QbD).The key steps and key process parameters were identified.The critical quality attributes (CQAs)of the intermediates and final product were clarified, the validation protocol and acceptable standard were accordingly developed, and the production process was validated.RESULTS:
The production process of parecoxib sodium freeze-dried preparation met the GMP requirements, and the intermediate and final products met the quality standards.CONCLUSION:
The established production process of parecoxib sodium freeze-dried preparation is feasible and the product quality is controllable.
Full text:
Available
Index:
WPRIM (Western Pacific)
Type of study:
Risk factors
Language:
Chinese
Journal:
Chinese Pharmaceutical Journal
Year:
2017
Type:
Article
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