Biotechnology laboratory software: Quality control

Our products for quality control and quality assurance
Any medicinal product is only as good as the quality of its manufacturing and testing processes. The very highest quality standards, and quick, safe processes in the biotechnology laboratory are among the key success factors for any company. Quality control tasks in regulated sectors of the pharmaceutical and biotechnology sectors cover the testing and release of raw materials, packaging and semi-finished products, right through to the finished medication. Key quality control tasks also include the continuous updating of test methods, including their validation, system capability and the calibration of laboratory equipment, as well as the review and monitoring of numerous reference standards. Medication for stability testing is also stored in the quality control department under controlled climatic conditions in accordance with the ICH guideline, and analysed until its expiry date. Dissolution testing is also carried out on solid dosage forms.

Our laboratory software products be used to support quality control and quality assurance tasks, and therefore save you time and money. Below is an overview indicating which LIMS can be used to meet your specific requirements:

  • Management of specifications, log plans, methods (LABS/Q)
  • Revalidation of a reworked method(VALIDAT/Method validation)
  •  Inspection order handling/deviation management/stability (LABS/Q)
  • Internal laboratory quality control (LABS/Q)
  • Graphic and statistical evaluations, reports (LABS/Q)
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