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    THIS PRESENTATION WILL TAKE YOU STEP BY STEP THROU 2013 - Webinar on BRC Risk Analysis - Webinar By GlobalCompliancePanel

    View: 334

    Website http://bit.ly/10Qo5Nq | Want to Edit it Edit Freely

    Category Webinar, Health, Pharma, Medical Device, FDA, Clinical

    Deadline: May 14, 2013 | Date: May 14, 2013

    Venue/Country: California, U.S.A

    Updated: 2013-04-30 18:08:16 (GMT+9)

    Call For Papers - CFP

    Overview: Risk Assessment is a fundamental and intuitive activity that is not new to manufacturing professionals. Bringing consciousness and tangibility to this process is the challenge often faced. A practical guide documenting the process will be the topic of this training.

    This presentation will take you step by step through the creation of each type of risk assessment required by the BRC. Process and product driven risk matrices will be presented. Sources of supporting documentation demonstrating the rationale utilized to arrive at conclusions will be provided. Quantification of risks and the progression to meaningful programs with defined goals.

    Why you should attend: Global Food Safety and US audit standards are becoming more and more aligned. While the numbering of items varies from one to the other, the criteria remain largely the same. Preparing for one audit is much like preparing for any other. However, There is a significant difference in the BRC certification requirements called risk assessments. There is approximately 27 risk assessment required throughout the quality systems standards. a review of the risk assessments is a critical part of the audit process. Conducting the risk assessments is also required for developing compliant as well as pertinent programs that lead to the achievement of quality systems objectives. What are the risk assessments that are needed and is there a way to tackle this seemingly insurmountable task? A practical approach to simplifying this process will be presented. By understanding the intent and utilizing a systematic process, the documentation of risk assessment can be easily accomplished bringing rigor and relevance to all the elements of the food safety and quality systems as well as facilitating a high performance result in the BRC certification audit.

    Areas Covered in the Session:

    Areas of the operation in which risks exist

    Sources of documentation

    Classification of risks

    documenting current processes for mitigating risks

    proposing risk reduction strategies

    Establishing timelines for process improvements

    Following up on proposed process improvements

    Application to regulatory and industry standards

    Sources of documentation

    Who Will Benefit:

    Senior Plant Management

    Corporate Division Leaders

    Document Authors and Editors

    Quality Assurance

    Melinda Allen is a Food Safety and Quality Consultant in the Food Industry. Melinda has had a long and dedicated career of Quality Assurance and Food Safety leadership with companies such as YUM Brands and Quiznos.

    Price: $165.00

    NetZealous LLC,

    DBA GlobalCompliancePanel

    161 Mission Falls Lane,

    Suite 216, Fremont, CA 94539, USA

    USA Phone:800-447-9407

    Fax: 302-288-6884

    webinarsatglobalcompliancepanel.com

    http://www.globalcompliancepanel.com

    Registration Link - http://bit.ly/10Qo5Nq


    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.