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    ONLINE TRAINING 2016 - Laboratory Accreditation: Getting there is just the beginning - By AtoZ Compliance

    View: 120

    Website http://bit.ly/203ASK7 | Want to Edit it Edit Freely

    Category laboratory accreditation, Quality Management System training, iso 17025 training, competency management training, quality management software

    Deadline: March 01, 2016 | Date: March 01, 2016

    Venue/Country: New Hyde Park, U.S.A

    Updated: 2016-02-05 17:31:59 (GMT+9)

    Call For Papers - CFP

    Key Take Away

    Overcoming the challenge by maintaining the quality management software to retain your accreditation status by ensuring staff adherence and ongoing compliance to minimize corrective actions arising from accreditation audits.

    Overview

    Developing a Quality Management System (QMS) as a prerequisite for getting accredited is relatively easy. Maintaining the quality management software to retain your accreditation status is the real challenge and a measure of the robustness of your System.

    Why Should You Attend

    Many laboratories struggle with developing and implementing functional quality management software that not only complies with the management and technical requirements of ISO/IEC 17025:2005 but also meets their needs. 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? Getting there is relatively easy. Staying there is the hard part.

    Areas Covered In This Webinar

    Defining a Quality Management System (QMS)

    Management Components of a QMS

    Technical Components of a QMS

    Method Selection, Validation and Verification

    What is competency management?

    Ensuring analyst competency

    Learning Objectives

    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?

    Who Will Benefit

    Laboratory Managers

    QA Managers

    QC Analysts

    Analytical support staff

    Laboratory quality development

    Speakers Profile

    Michael Brodsky Michael has been an Environmental Microbiologist

    for more than 42 years. He is a Past President of the Ontario Food Protection Association (OFPA), the International Association for Food Protection (IAFP) and AOAC International. He serves as Chair for the AOAC Expert Review Committee for Microbiology, as a scientific reviewer in Microbiology for the AOAC OMA and the AOAC Research Institute, as a reviewer for Standard Method for the Examination of Water and Wastewater and as a chapter editor on QA for the Compendium of Methods in Microbiology. He is also a lead auditor/assessor in microbiology for the Canadian Association for Laboratory Accreditation (CALA) and is Vice-chair of the CALA Board of Directors.

    For more detail please click on this below link:

    http://bit.ly/203ASK7

    Email: referralsatatozcompliance.com

    Toll Free: +1- 844-414-1400

    Tel: +1-516-900-5509


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.