Accrediations - DNA Labs India
Accrediations DNA Labs India
DNA Labs India, Our Quality Management Statement: Management is committed to being very aggressive in our attitude towards quality of our testing in servicing our customers, good professional practices and customer service, primarily since we want to be ranked as the "best" in our business. Our employees remain clearly focused on the Quality System, so they will effectively implement the policies and procedures in their casework and quality control functions.
A2LA The A2LA is the largest multi-discipline laboratory accreditation system in the United States and is recognized by Accreditation Bodies in the European Union, Asia and other International Communities. A2LA accreditation imposes stricter requirements than ISO 17025: 2005 certification alone, particularly focusing on technical competence, traceability of measurements and the overall proficiency of the laboratory.
A2LA is a non-profit, non-governmental, public service, membership society whose mission is to: meet the needs of both laboratories and their users for competent testing; improve the quality of laboratories and the data they produce; and increase acceptance of accredited laboratory data to facilitate trade, based on internationally accepted criteria for competence (ISO / IEC 17025:2005).
ISO 9001 In light of the amendment of ISO 9001:2008, the International Accreditation Forum (IAF), the International Laboratory Accreditation Cooperation (ILAC), and the International Organization for Standardization (ISO) have issued a revised communiquÃ© declaring that the management system requirements of ISO/IEC 17025 meet the principles of ISO 9001:2008.
The College of American Pathologists (CAP) The College of American Pathologists, the principal organization of board-certified pathologists, serves and represents the interest of patients, pathologists, and the public by fostering excellence in the practice of pathology and laboratory medicine.
Food and Drug Administration DNA Labs India testing DNA kits contain sterile components specifically designed for collection of samples requiring analysis using current DNA profiling techniques. Lancets are sterilized in accordance with ANSI/AMMI/ISO Guidelines and are validated as â€œsterileâ€ by third party FDA registered facilities. You may have total confidence in knowing that the products used to collect your samples are in compliance with the strictest requirements in the world, ensuring your safety and personal health.
ILAC-MRA The International Laboratory Accreditation Cooperation (ILAC) first started as a conference in 1977 with the aim of developing international cooperation for facilitating trade by promotion of the acceptance of accredited test and calibration results. In 1996, ILAC became a formal cooperation with a charter to establish a network of mutual recognition agreements among accreditation bodies that would fulfill this aim. The ILAC Mutual Recognition Arrangement (often referred to as the ILAC Arrangement) is the culmination of 22 years of intensive work.
The arrangement came into effect on 31 January 2001. The ILAC Arrangement provides significant technical underpinning to international trade. The key to the Arrangement is the developing global network of accredited testing and calibration laboratories that are assessed and recognized as being competent by ILAC Arrangement signatory accreditation bodies. The signatories have, in turn, been peer-reviewed and shown to meet ILAC's criteria for competence. Now that the ILAC Arrangement is in place, governments can take advantage of it to further develop or enhance trade agreements. The ultimate aim is increased use and acceptance by industry as well as government of the results from accredited laboratories, including results from laboratories in other countries. In this way, the free-trade goal of "a product tested once and accepted everywhere" can be realized.
CLIA US government passed the Clinical Laboratory Improvement Amendments (CLIA) in 1988 establishing quality standards for all laboratory testing to ensure the accuracy, reliability and timeliness of patient test results regardless of where the test was performed. A laboratory is defined as any facility which performs laboratory testing on specimens derived from humans for the purpose of providing information for the diagnosis, prevention, treatment of disease, or impairment of, or assessment of health. CLIA is user fee funded; therefore, all costs of administering the program must be covered by the regulated facilities.