News
The active pharmaceutical ingredient (API) production facility is taking multiple measures to ensure the smooth implementation of the new version of Pharmaceutical GMP.
Date:
01 Mar,2021
During Wanbang Pharmaceutical's comprehensive rollout of the new GMP implementation in 2013, the active pharmaceutical ingredient (API) production facility adopted multiple measures to ensure robust management across all operational stages.
First, in accordance with Wanbang Pharmaceutical Document No. 45 [2013], "Work (Training) Outline for Fully Implementing the New GMP Management System," we will appropriately reallocate personnel and organize participation in the GMP training sessions hosted by headquarters. To meet Wanbang Pharmaceutical's enhanced training requirements, all positions within the facility will intensify their training efforts, ensuring widespread adoption of the new GMP training program.
Second, in line with the key features of the revised GMP guidelines, we are making every effort to strengthen our quality management system, raising the standards for companies' quality management software. Additionally, we are ensuring the development and implementation of standardized operating procedures (SOPs) and relevant documentation across all workshops within the facility.
Furthermore, in alignment with the "Environmental Improvement" initiative, we are introducing new corrective measures aimed at enhancing safety management, environmental protection practices, and clean production processes throughout the plant.
Third, ensure the comprehensive implementation of maintenance, repairs, and upkeep for production equipment, process pipelines, as well as the calibration of utilities, instruments, and weighing devices across all production workshops. The workshops have scheduled 35 days in the fourth quarter to complete the newly launched Ciprofloxacin (final drying and packaging) project, the Chlorpromazine project, and the renovation of the cafeteria and office spaces.
Meanwhile, to enhance overall management effectiveness, a dedicated departmental evaluation system has been implemented to ensure the smooth rollout of the new GMP guidelines.
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