Why You Should Use a QC Laboratory Service
Eradicating the risk of anomalous results is the main objective of a quality management system. Quality control and quality assurance programs aim to provide precise results by practiced policies, processes, and procedures. In particular, the role of internal quality control (QC) is to ensure that the quality of results produced via laboratory testing meets standards consistently.
Why should you use a QC laboratory service? A quality control laboratory assists assorted business facilities, companies, and organizations by assuring safety and efficiency in their methodology and product development. Working alongside a QC laboratory—through concept, intermediate, or final stages—safeguards the accuracy, timeliness, and reliability of results. Let’s examine the advantages of these quality control services more closely.
Detect and Minimize Laboratory-Originated Errors
Laboratory errors tend to occur during diverse experimental or development stages, including the pre-analytical, analytical, and post-analytical stages. A wide range of errors can occur, from material mishandling, unsuitable transfer, or incorrect sample collection. Errors can arise during testing processes due to non-adherence to standard operating procedures or the use of non-calibrated or unqualified equipment. Not to mention, the incorrect recordkeeping and interpretation of specific analysis results can also cause errors.
Reliable QC laboratory services are the solution to the above mismanagements or oversights. Remember that proficient staff management is essential, as this team is the most critical lab resource.
Verify Consistency in Active Ingredient Levels
Verifying consistency is another reason why you should use a QC laboratory service. Quality control concerns the correct management of laboratory inventory, processes, environmental conditions, and documentation. Whether developing a new clinical product or approach, QC analytical services are key prevention strategies to avoid compromising quality of care. Proper evaluation and purification of active ingredient feasibility and stability provides assurance of safety and performance.
Ensure Reliability and Compliance With Industry Standards
Failure to utilize a QC-integrated laboratory can lead to numerous consequences, including time wastage, further budget implications, loss of customer or client satisfaction, and safety concerns due to non-compliance with industry standards.
Quality control mechanisms are especially essential in the pharmaceutical field, as errors can impact patient diagnosis and treatment. For this reason, laboratory-set QC measures are the fundamental building blocks of certified and accredited operations.
Moravek offers cGMP quality control and analytical services for method development, transfer, storage, and API stability studies. As a trusted contract manufacturer of cGMP radiolabeled active pharmaceutical ingredients, we understand the necessary requirements for QC-qualified systems and current good manufacturing practices support. Our dedicated QC laboratory contains qualified analytical equipment operated by highly-proficient staff to complete our variety of exceptional services. Learn more about Moravek Quality on our website today.