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      <title>Integrated Food Safety Traceability Systems - traceability capabilities, costs and trends</title>
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      <description>This Food Safety system webinar will discuss how the current traceability capabilities, costs and trends will become integrated into food safety systems and explore the different approaches like Barcode, RFID, Manual systems, simple tagging etc.</description>
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      <title>Design Validation Protocol and Acceptance Criteria for Chromatographic Methods to meet ICH requirements</title>
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      <description>Key validation characteristics of HPLC methods mandated according to cGMP and ICH guidelines and the stress studies must be considered for HPLC method used in pharma Labs.</description>
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      <title>Record Keeping for a food Recall: Keeping Records to Minimize the Affect of a Recall</title>
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      <description>This Food safety training will provide valuable guidance to management, supervision, and quality staff that are involved with record keeping for product and ingredient traceability and recall.</description>
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      <title>How to implement parametric release in EO sterilization-Practical approach</title>
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      <description>This EO sterilization training will discuss the Cycle validation and other requirements for Implementation of parametric release in EO sterilization as per EN/ISO 11135.</description>
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      <title>Out-of-Specification Investigations – Beyond the laboratory</title>
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      <description>This Out-of-Specification Investigations webinar will begin with the confirmed out-of-specification laboratory result and discuss how the investigation is expanded into the whole organization.</description>
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      <title>Understanding Disinfectant Qualification Studies – How to avoid errors</title>
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      <description>Technical details need to know about the disinfectant qualification study, data review, how to evaluate log reductions, how to use study data for routine clean room cleaning operations.</description>
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      <title>Validating Radiation Sterilization for medical device industries</title>
      <link>http://www.complianceonline.com/ecommerce/control/trainingFocus?product_id=701604&amp;channel=rss_organic</link>
      <description>This Radiation sterilization will discuss how radiation sterilization works, the equipment involved, major issues with product sterilization via radiation, and the validation requirements.  Routine process control and monitoring will be reviewed along with requirements to maintain the process effectiveness.</description>
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      <title>How to comply with recent expectations for Extractables /Leachables testing for Biologics</title>
      <link>http://www.complianceonline.com/ecommerce/control/trainingFocus?product_id=701591&amp;channel=rss_organic</link>
      <description>This Webinar will discuss the test conditions of Extractables/Leachables and also the requirements for testing extractables/Leachables.</description>
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      <title>21 CFR Part 11: Ins and Outs of Audit Trails</title>
      <link>http://www.complianceonline.com/ecommerce/control/trainingFocus?product_id=701612&amp;channel=rss_organic</link>
      <description>This 21 CFR Part 11 training will provide types of audit trails and Strategies of implementing compliant audit trails as per 21 CFR Part 11 regulations.</description>
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      <title>SOP Development for Medical Device Firms: Utilizing “lean compliance” principles to meet your quality system documentation requirements</title>
      <link>http://www.complianceonline.com/ecommerce/control/trainingFocus?product_id=701590&amp;channel=rss_organic</link>
      <description>This Webinar will discuss how to develop SOPs with principles and skills to ensure the SOPs are simply the result of a well defined and sound processes and also meets FDA or ISO requirements.</description>
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