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Notice of the Office of the Sichuan Provincial Drug Administration on Issuing the Implementation Plan for the Quality Supervision and Sampling Inspection of Sichuan Pharmaceutical Packaging Materials in 2020
- Categories:Local Regulations
- Author:
- Origin:
- Time of issue:2020-05-11
- Views:
Notice of the Office of the Sichuan Provincial Drug Administration on Issuing the Implementation Plan for the Quality Supervision and Sampling Inspection of Sichuan Pharmaceutical Packaging Materials in 2020
- Categories:Local Regulations
- Author:
- Origin:
- Time of issue:2020-05-11
- Views:
Municipal (prefecture) Market Supervision Administration, Provincial Food and Drug Inspection and Testing Institute:
Now the "2020 Sichuan Province Pharmaceutical Packaging Material Quality Supervision and Sampling Inspection Implementation Plan" is issued to you, and the following requirements are put forward, please implement them together.
1. The Provincial Drug Administration (hereinafter referred to as the Provincial Bureau) is responsible for organizing and implementing the supervision and sampling of pharmaceutical packaging materials this year, and the Provincial Food and Drug Inspection and Testing Institute is responsible for the sampling, inspection and evaluation of pharmaceutical packaging materials this year. Each city (prefecture) Market Supervision Administration assists the Provincial Food and Drug Inspection and Testing Institute to carry out on-site sampling and inspection of the companies that produce and use pharmaceutical packaging materials in their jurisdictions (pharmaceutical packaging material manufacturers, pharmaceutical manufacturers, and preparation rooms of medical institutions).
2. The Provincial Food and Drug Inspection and Testing Institute shall carry out sampling and testing in a timely manner. The inspection report of qualified samples shall be directly sent to the units selected for inspection and submitted to the provincial bureau; all the inspection reports of unqualified samples shall be submitted to the provincial bureau, and the provincial bureau will organize investigation and processing.
3. The funds for this supervision and random inspection will be covered by the provincial financial special funds, and no fees shall be collected from the sampled units.
Fourth, the Provincial Food and Drug Inspection and Testing Institute will submit the evaluation and analysis report to the provincial bureau before December 30, 2020, based on the product sampling.
Annex: 2020 Sichuan Province Pharmaceutical Packaging Material Quality Supervision and Sampling Implementation Plan
Sichuan Provincial Drug Administration Office
May 11, 2020
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