These details need to be documented in a manner that can be easily presented during an audit to demonstrate laboratory compliance.
Ideally, the results of any tests are stored alongside the samples. It is also important to make sure that automatic systems are implemented to maintain sample testing timelines and ensure that the right testing is performed and completed on time. The right systems need to be in place to track the samples being tested, the assignments of those samples to scientists, and the specific attributes to be tested. This includes making note of any sample handling that occurs along the way. A LIMS is optimized and is validated out-of-the-box to address quality issues that commonly arise in laboratories.ġ0 Ways that QC Lab Managers Can Use LIMS Sample TrackingĪccountability is a key component of running an effective, compliant lab. The implementation of a laboratory information management system (LIMS) can make all the difference for laboratory operations, primarily through its capacity for automation and documentation. To some extent, these professionals have to rely on the rest of the laboratory to meticulously follow best practices, but even in the best-case scenario, the lab is still vulnerable to human error. This team is responsible for ensuring the quality and purity of pharmaceutical ingredients and products, where there is no room for error.Įnsuring that the lab staff is properly trained, actively maintaining the appropriate procedures, and documenting lab activity in an audit-compliant manner can be an overwhelming list for a QC lab manager. Although all laboratories must comply with industry standards in order to produce valid results, the pharmaceutical laboratory’s quality control (QC) team must adhere to some of the most stringent standards.
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