Understanding and Implementing an Effective Laboratory Quality Practice System : ISO 1725
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Category ISO 17025 Training; Good Laboratory Practice Training
Deadline: April 02, 2018 | Date: April 02, 2018
Venue/Country: Training Doyens 26468 E Walker Dr,Aurora, Colora, U.S.A
Updated: 2018-02-16 20:02:31 (GMT+9)
Call For Papers - CFP
OVERVIEWPart 1QMS is the catch phrase for accreditation and is the backbone of ISO/IEC Standard 17025: The Quality System Manual (QSM) is the bible in a QMS environment because, much like its predecessor, Good Laboratory Practice (GLP), it contains the policies that the laboratory is expected to follow to achieve quality results. It is in fact only the “what to do” component of a QMS. What is also needed are the “how to do it” or procedures and methods and finally the controls or evidence that it was done properly. This is the 1st of two webinars on this topic and focuses on complying with themanagement requirements of the standard.Part 2Many laboratories regard Quality Assurance, Quality Assessment and Quality Control as independent activities, others use the terms interchangeably, e.g. QA/QC. This demonstrates a lack of appreciation of the differences between Assurance, Assessment and Control, as well as the interrelationships, particularly between QA and QC. This has created confusion in the minds of many analysts with respect to understanding how QA and QC play separate, but related roles for achieving Quality Assurance in a Quality Management System (QMS).WHY SHOULD YOU ATTENDPart 1Accreditation to international standards is becoming the norm in the global analytical community. Although essentially voluntary, there are many jurisdictions that now require food and environmental laboratories to be accredited to ISO/IEC 17025 in order to participate in regulatory programs. Once accreditation has been achieved many laboratories have difficulty maintaining the QMS as evidenced by the number of non-conformances cited during the subsequent biannual audits. Why do you want to become accredited? Where do you start? For laboratories that are already accredited, how do you ensure staff adherence and ongoing compliance to minimize corrective actions arising from accreditation audits? Many laboratories struggle with developing and implementing a functional quality management system that not only complies with the management and technical requirements of ISO/IEC 17025b but also meets their own needs and those of their customers.Part 2QMS is the catch phrase for accreditation and is the backbone of ISO/IEC Standard 17025:Accreditation to international standards is becoming the norm in the global analytical community. Although essentially voluntary, there are many jurisdictions that now require food and environmental laboratories to be accredited to ISO/IEC 17025 in order to participate in regulatory programs. This webinar is the 2nd in the series and will address how to develop and maintain the technical components of the QMS.AREAS COVEREDPart 1Management Components of a QMSDocument ControlQuality SystemReview of Requests, Tenders and ContractsSubcontracting of Tests and CalibrationsPurchasing Services and SuppliesService to CustomerControl of Non-conforming Testing and/or Calibration WorkControl of RecordsInternal AuditsManagement ReviewPersonnelPart 2Accommodation and Environmental ConditionsTest and Calibration Methods and Method ValidationEquipmentMeasurement TraceabilitySamplingHandling of Test and Calibration ItemsAssuring the Quality of Test and Calibration ResultsLEARNING OBJECTIVESPart 1Policies vs. ProceduresDocuments vs. RecordsThe importance of the KISS principleThe devil’s in the detailsPart 2Technical Requirements of a QMSMethod Selection Validation and VerificationEnsuring analytical competencyWHO WILL BENEFITLaboratory Management/SupervisionLaboratory Quality DevelopmentLaboratory Quality ManagementLaboratory Quality ControlAnalytical supportFor more details click on this link:http://bit.ly/2EKtLBn You may also refer to this link:https://www.trainingdoyens.com/product/50103-data-integrity-&-cgmp-compliancehttps://www.trainingdoyens.com/product/50159-failure-mode-and-effect-analysis
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