{"id":7972,"date":"2023-06-26T15:32:23","date_gmt":"2023-06-26T05:32:23","guid":{"rendered":"http:\/\/anitechgroup.com\/au\/?p=7972"},"modified":"2023-06-27T14:50:46","modified_gmt":"2023-06-27T04:50:46","slug":"quality-management-for-laboratories-a-complete-overview","status":"publish","type":"post","link":"https:\/\/anitechgroup.com\/au\/blog\/quality-management-for-laboratories-a-complete-overview\/","title":{"rendered":"Quality Management for Laboratories: A Complete Overview\u00a0"},"content":{"rendered":"<p>Quality Management for Laboratories ensures the accuracy and reliability of test results. This blog will dive into the concept of laboratory quality management, discussing its definition, importance, benefits, and implementation process.<\/p>\n<h2>Definition of Laboratory Quality Management<\/h2>\n<p>Quality management for laboratories refers to the systematic approach used in laboratories to maintain high proficiency and performance standards. It involves establishing protocols and procedures that govern every aspect of laboratory work, from sample collection and processing to analysis and reporting. The ultimate goal of quality management for laboratories is to ensure that test results are accurate, reliable, and meaningful for decision-making purposes.<\/p>\n<h2>Importance of Laboratory Quality Management<\/h2>\n<p>Ensuring high-quality performance in a lab has several crucial implications for businesses, scientific research institutions, healthcare providers, and other stakeholders. The integrity of laboratory data directly affects decision making processes and can have significant consequences in various industries such as pharmaceuticals, food safety, environmental monitoring, etc.<\/p>\n<p>In healthcare settings, accurate lab results can be critical for diagnosis or determining a patient&#8217;s treatment options. Similarly, businesses may rely on laboratory analyses to ensure product quality or compliance with regulatory requirements. In such cases, errors in reporting can lead to severe financial losses or even legal issues for the stakeholders involved.<\/p>\n<h2>Benefits of Laboratory Quality Management<\/h2>\n<p>Implementing a robust laboratory quality management system offers several benefits:<\/p>\n<p>Improved Accuracy:\u202fFocusing on proper training and standardising procedures throughout the lab decreases the chance of human errors.<\/p>\n<h3>1. Enhanced Efficiency:<\/h3>\n<p>Streamlined workflows and better resource allocation lead to faster lab result turnaround times.<\/p>\n<h3>2. Cost Reduction:<\/h3>\n<p>Minimising errors reduces the need for retesting samples or running additional tests due to unreliable initial results.<\/p>\n<h3>3.\u00a0 Compliance:<\/h3>\n<p>Laboratories adhering to quality management systems are more likely to meet regulatory requirements set by accrediting agencies such as ISO\/IEC 17025, CAP, and CLIA.<\/p>\n<h3>4.\u00a0 Increased Confidence:<\/h3>\n<p>Implementing a quality management system enables laboratories to provide accurate and reliable results to clients and stakeholders, ultimately building trust in the lab&#8217;s capabilities.<\/p>\n<h2>Process of Implementation<\/h2>\n<p>Implementing a laboratory quality management system involves a series of steps:<\/p>\n<h3>1. Establish Policies and Objectives:<\/h3>\n<p>Define the lab&#8217;s commitment to quality and set measurable goals in line with international standards or accreditation requirements.<\/p>\n<h3>2.\u00a0 Develop Written Procedures and Protocols:<\/h3>\n<p>Create detailed guidelines for all laboratory operations, including sample handling, equipment usage, data management, and reporting.<\/p>\n<h3>3. Train Staff:<\/h3>\n<p>Ensure all staff members are proficient in the lab&#8217;s standard operating procedures (SOPs) and understand their roles in maintaining quality.<\/p>\n<h3>4.\u00a0 Allocate Resources:<\/h3>\n<p>Provide adequate funding, staffing, and infrastructure necessary to maintain high-quality standards.<\/p>\n<h3>5. Monitor Performance:<\/h3>\n<p>Regularly evaluate the effectiveness of the implemented quality management system using internal audits, performance indicators, proficiency testing, and customer feedback.<\/p>\n<h3>6.\u00a0 Continuous Improvement:<\/h3>\n<p>Identify areas for improvement based on monitoring results and make appropriate changes to the system.<\/p>\n<ul>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"17\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\">Determine the components of excellent laboratory practice and the organisation&#8217;s specific quality needs.<\/li>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"17\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\">Put in place a management structure to achieve efficient control over laboratory operations;<\/li>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"17\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\">Cater to client needs and accreditation standards.<\/li>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"17\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;hybridMultilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\">Use risk-based thinking and best practices to continually enhance the laboratory&#8217;s operations.<\/li>\n<\/ul>\n<h2>Best Practices for Laboratory Quality Management<\/h2>\n<p>Here are some key best practices for laboratory quality management in Australia:<\/p>\n<h3>1. Compliance with ISO\/IEC 17025:<\/h3>\n<p>ISO\/IEC 17025 is the global standard for testing and calibration laboratories. Ensuring compliance with this standard is essential for demonstrating technical competence, maintaining reliable results, and meeting customer requirements.<\/p>\n<h3>2. Document Control:<\/h3>\n<p>Establish a robust document control system to manage and control laboratory documents, including standard operating procedures (SOPs), work instructions, and test methods. This system should ensure that documents are up-to-date, accessible to authorised personnel, and properly version controlled.<\/p>\n<h3>3. Competence and Training:<\/h3>\n<p>Develop a comprehensive training program for laboratory staff to ensure they have the required skills, knowledge, and competencies to perform their tasks accurately. Training should cover technical procedures, safety protocols, quality management principles, and regulatory compliance.<\/p>\n<h3>4. Equipment Calibration and Maintenance:<\/h3>\n<p>Implement a proactive calibration and maintenance program to ensure the accuracy and reliability of laboratory equipment. Develop schedules for calibration, verification, and maintenance activities and maintain detailed records of these activities.<\/p>\n<h3>5. Quality Control and Quality Assurance:<\/h3>\n<p>Implement a robust quality control program to monitor and verify the performance of analytical methods, instruments, and reagents. This includes internal quality control checks, participation in external proficiency testing programs, and regular equipment performance verification.<\/p>\n<h3>6.\u00a0 Sample Handling and Chain of Custody:<\/h3>\n<p>Develop and implement clear procedures for sample handling, including proper identification, labelling, storage, and transportation. Implement a chain of custody process to ensure the integrity and traceability of samples throughout their lifecycle.<\/p>\n<h3>7.\u00a0 Data Management and Integrity:<\/h3>\n<p>Establish a secure and reliable data management system to ensure accurate record-keeping, data integrity, and traceability. This includes proper data entry validation, secure storage, regular data backups, and access controls to protect sensitive information.<\/p>\n<h3>8.\u00a0 Risk Management:<\/h3>\n<p>Implement a systematic approach to identify, assess, and manage risks associated with laboratory processes. Conduct risk assessments to identify potential hazards, prioritise risks, and develop risk mitigation strategies.<\/p>\n<h3>9.\u00a0 Continuous Improvement:<\/h3>\n<p>Foster a culture of continuous improvement within the laboratory. Encourage staff to identify opportunities for improvement, implement corrective actions, and share lessons learned. Regularly review laboratory processes, performance metrics, and customer feedback to drive continuous improvement.<\/p>\n<h3>10.\u00a0 External Audits and Accreditation:<\/h3>\n<p>Consider seeking accreditation from a recognised accreditation body, such as the National Association of Testing Authorities (NATA) in Australia. External audits and accreditation provide independent validation of the laboratory&#8217;s competence and adherence to international standards.<\/p>\n<h2>What is Good Laboratory Practice (GLP)?<\/h2>\n<p>GLP is a quality system that addresses organisational procedures and requirements for nonclinical health and environmental safety studies&#8217; design, execution, monitoring, recording, archiving, and reporting.<\/p>\n<p>One of the following categories best describes GLP studies:<\/p>\n<p>Physical-chemical, toxicity, mutagenicity, environmental toxicity, bioaccumulation, residue, effects on mesocosms and the natural ecosystem, safety studies of medical devices, analytical and clinical chemistry related to nonclinical studies, verification of virus inactivation, and statistical analysis of data are some of the topics covered.<\/p>\n<h3>Organisation for Economic Cooperation and Development OECD Principles of GLP<\/h3>\n<p>The Organisation for Economic Cooperation and Development (OECD) created the Principles of GLP in the late 1970s to encourage the creation of test data of comparable quality and to serve as the cornerstone of the Mutual Acceptance of Data (MAD) agreement between OECD member countries and non-member countries that abide by the agreement. Under the terms of the agreement, reliance on test data enables avoidance of redundant testing, removal of trade barriers, and time and resource savings while enhancing environmental and human health protection.<\/p>\n<p>The test items in medicines, insecticides, cosmetics, veterinary medications, food additives, feed additives, and industrial chemicals are all subject to the principles.<\/p>\n<p>Clinical research does not fall within the principles.<\/p>\n<p>Organisations can request copies of the OECD Principles and any accompanying documentation from the OECD Environment Directorate.<\/p>\n<h3>Australian GLP program<\/h3>\n<p>Any Australian facility conducting nonclinical health and environmental safety investigations is eligible for recognition by NATA for conformity with the OECD Principles.<\/p>\n<p>Regulations may call for these investigations to register or licence medicines, insecticides, veterinary drugs, and similar items, as well as to control industrial chemicals.<\/p>\n<p>Nonclinical health and environmental safety investigations must also be carried out per the OECD Principles of GLP, according to most foreign regulatory bodies.<\/p>\n<p>Several Australian regulatory organisations are in charge of evaluating, regulating, and managing chemicals in Australia.<\/p>\n<p>These include:<\/p>\n<ul>\n<li>Agency Product<\/li>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"14\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\">Therapeutics Goods Administration (TGA)<\/li>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"14\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\">Pharmaceutical<\/li>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"14\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\">Australian Pesticide and Veterinary<\/li>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"14\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"4\" data-aria-level=\"1\">Medicine Authority (APVMA)<\/li>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"14\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"5\" data-aria-level=\"1\">(Formerly the National Registration Authority (NRA))<\/li>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"14\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"5\" data-aria-level=\"1\">Veterinary and agricultural chemicals<\/li>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"14\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"5\" data-aria-level=\"1\">Australian Industrial Chemicals<\/li>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"14\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"5\" data-aria-level=\"1\">Introduction Scheme (AICIS)<\/li>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"14\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"5\" data-aria-level=\"1\">Industrial chemicals<\/li>\n<\/ul>\n<h3>GLP Recognition for Overseas Test Facilities<\/h3>\n<p>Under the Mutual Acceptance of Data (MAD) instructions, NATA is solely required to evaluate Australian facilities. The OECD Principles include these guidelines in full. They indicate that if data is created in a facility that is acknowledged as complying with GLP by the national GLP compliance monitoring body, then it must be recognised worldwide for the purposes of evaluation by OECD member nations and non-member countries (who agree to the MAD guidelines).<\/p>\n<p>Facilities situated in nations that follow the MAD instructions may request GLP recognition by contacting the appropriate national GLP compliance monitoring body. The OECD website&#8217;s GLP section has a list of them.<\/p>\n<p>Suppose the appropriate Australian regulator requests an inspection, and the facility is situated in a nation without a GLP compliance monitoring authority that complies with MAD instructions. In that case, NATA may then conduct the inspection.<\/p>\n<p>In such circumstances, regulators from other nations need not accept the findings of the NATA evaluation of these foreign plants. The facility would be included in NATA&#8217;s yearly report to the OECD GLP Working Group, but it would not be monitored for GLP compliance in Australia. It would not be eligible to receive accreditation from that country&#8217;s programme.<\/p>\n<h2>Reporting to other GLP Compliance Monitoring Authorities<\/h2>\n<p>All GLP compliance monitoring organisations receive a yearly report from NATA via the OECD. The facilities in the Australian programme and their current GLP standing are included in this report.<\/p>\n<p>NATA reports any research or facilities found to be in violation of GLP standards to the Australian regulators and all members of the OECD GLP Working Group.<\/p>\n<h3>Roles and Responsibilities of GLP Sponsors<\/h3>\n<p>The organisation that commissions, funds, supports, and\/or submits nonclinical health and environmental safety research is known as the Sponsor.<\/p>\n<p>The Sponsor should be aware of the OECD Principles&#8217; obligations, especially those pertaining to the test facility&#8217;s administration and the Study Director\/Principal Investigator&#8217;s duties.<\/p>\n<h3>NATA&#8217;s Criteria for GLP Recognition<\/h3>\n<p>Additional NATA publications also support the OECD Principles used to recognise facilities. The NATA Procedures for Accreditation describe the &#8220;package&#8221; of documents that apply to GLP.<\/p>\n<p>It is also adviced that facilities looking to be recognised for adhering to the OECD Principles apply for ISO\/IEC 17025 accreditation for the testing component of their GLP activities. The latter standard&#8217;s accreditation grants technical competency recognition.<\/p>\n<h4>Steps to NATA GLP Recognition<\/h4>\n<p>Below given are the key steps in the NATA GLP recognition Process:<\/p>\n<ul>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"15\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"1\" data-aria-level=\"1\">Enquiry<\/li>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"15\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"2\" data-aria-level=\"1\">Advisory Visit<\/li>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"15\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"3\" data-aria-level=\"1\">Application<\/li>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"15\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"4\" data-aria-level=\"1\">Document Review<\/li>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"15\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"4\" data-aria-level=\"1\">Assessment<\/li>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"15\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"4\" data-aria-level=\"1\">Recognition<\/li>\n<li data-leveltext=\"\uf0b7\" data-font=\"Symbol\" data-listid=\"15\" data-list-defn-props=\"{&quot;335552541&quot;:1,&quot;335559684&quot;:-2,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;\uf0b7&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}\" data-aria-posinset=\"4\" data-aria-level=\"1\">Scheduled Reassessments and Study Audits<\/li>\n<\/ul>\n<p>It is recommended to seek guidance from relevant regulatory bodies and engage with quality management experts to tailor these practices to the specific needs of your laboratory.<\/p>\n<p>Anitech QMS consultants can help.<\/p>\n<p>To book a consulting session and benefit from our services, call us at 1300 802 163 or e-mail \u2013\u202f<a href=\"mailto:sales@anitechgroup.com\">sales@anitechgroup.com<\/a><\/p>\n<p>For more information, stay tuned to the Anitech website.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Quality Management for Laboratories ensures the accuracy and reliability of test results. This blog will dive into the concept of laboratory quality management, discussing its definition, importance, benefits, and implementation process. Definition of Laboratory Quality Management Quality management for laboratories refers to the systematic approach used in laboratories to maintain high proficiency and performance standards&#8230;.<\/p>\n","protected":false},"author":1,"featured_media":7989,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"content-type":"","inline_featured_image":false,"footnotes":""},"categories":[1,172],"tags":[],"ppma_author":[253],"class_list":["post-7972","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-blog","category-quality-management-system-iso-9001"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Quality Management for Laboratories: A Complete Overview\u00a0<\/title>\n<meta name=\"description\" content=\"Quality management for laboratories refers to the systematic approach used in laboratories to maintain 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