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СATALOGUE / AUTOMATION OF PHARMACEUTICAL PRODUCTION / Organization of output quality control of products

Organization of output quality control of products

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СATALOGUE / AUTOMATION OF PHARMACEUTICAL PRODUCTION / Organization of output quality control of products

Organization of output quality control of products

Every drug manufacturing facility has a quality control department (QCD) that is independent of other departments. The head of this department should have the necessary experience and qualifications. The quality control department includes one or more control laboratories. The department must be provided with all the necessary resources to perform its functions.
The in-process control of products is carried out according to the control points specified in the industrial regulations.

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  • Information updated : 10 / 10 / 2024
  • In stock
  • Manufacturer : 1 year for Organization of output quality control of products

Model: Organization of output quality control of products

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The selected control samples shall be a representative sample of the product series. The sample shall be taken in its entirety for physicochemical testing, taking into account the performance of arbitration tests. The tare place, from which the sample was taken, shall be identified by the JCC controller with the label “Sampling”. On the basis of the obtained test results, a passport for the finished product signed by the head of the JCC is drawn up. Products that have passed quality control are moved to the enterprise’s finished product warehouse.

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Articles  — A genre of journalism in which the author sets the task of analyzing social situations, processes, phenomena, primarily from the point of view of the regularities underlying them.
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Technical specifications

Quality control in the production process is carried out by the shop laboratory staff and production personnel in accordance with the technological documentation. All operations on in-process control (including operations performed by persons directly working in production areas) shall be carried out in accordance with the methods approved by the JCC.

Additional information

The results of in-process control are documented. Output control of finished products is carried out by QAQC in accordance with the indicators of the pharmacopoeial article or regulatory documentation. Sampling should be carried out in accordance with the approved instructions. Labeled and packaged finished products are submitted to the JCC for acceptance control simultaneously the entire series. Sampling of finished product in consumer packaging is carried out by the QAC controller selectively in the “Quarantine” zone of the workshop warehouse.

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