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      <title>OSHA&amp;apos;s Update of Hazard Communication: What it Means for You</title>
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      <description>This 90-minute webinar will cover the OSHA’s new Hazard Communication Standard and will  discuss the differences between the old standard and the new standard so that attendees will  be able to adapt and apply the requirements in the workplace.</description>
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      <title>Supplier Controls to Meet Tougher U.S. FDA Requirements</title>
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      <description>This 90-minute webinar on supplier controls will help you refine your supplier management and audits to match the FDA&amp;apos;s tougher position. We will evaluate the chief areas of change to see how to better prepare a supplier chain management and audit program.</description>
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      <title>Best Practices for Medical Device Reporting (MDR), Recall, Reports of Corrections and Removals</title>
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      <description>This 90-minute webinar will discuss the requirements and compliance under the applicable FDA regulations for medical device reporting (MDR), recall and reports of corrections and removals in the US. It is designed to help the audience develop, maintain and implement adequate procedures.</description>
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      <title>Validation of Existing/ Legacy Computer Systems for FDA/EU Compliance</title>
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      <description>This webinar on validating legacy computer systems will give a good understanding of FDA and EU regulatory requirements for validation (retrospective validation) and provide tools for effective implementation.</description>
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      <title>FDA Warning Letter - Consent Decree Software Validation</title>
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      <description>This FDA warning letter Webinar/training will discuss what to do to avoid additional software related compliance along with the response steps where the citations that directly or indirectly include automated system.</description>
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      <title>3-hr Virtual Seminar - Affirmative Action Compliance and Your Recruiting Strategy: Pulling it together</title>
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      <description>This 3-hr virtual seminar will take a deeper look at your recruiting practice and review the objective for affirmative action as it relates to this function in terms of ensuring compliance.  The session also features a discussion about how to make the most of your recruiting technology so that you are prepared to meet the OFCCP’s recently heightened enforcement efforts.</description>
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      <title>An Overview of Risk Management and Risk Analysis Techniques in Clinical Trials</title>
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      <description>This webinar will provide you with an overview of risk factors in clinical trials and discuss possible ways to mitigate, control, assess impact, and prevent them in your trial.</description>
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      <title>Pre-Approval Statements and Representations by Pharmaceutical Manufacturers</title>
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      <description>This 90-minute webinar will help you understand the problems that can occur with statements by pharmaceutical manufacturers directed to off-label uses of pharmaceuticals.</description>
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      <title>Making Sense of FDA’s (proposed) Rules for the Development and Approval of Biosimilars</title>
      <link>http://www.complianceonline.com/ecommerce/control/trainingFocus?product_id=702325&amp;channel=rss_organic</link>
      <description>This webinar will help you understand the process, requirements, quality and safety considerations for demonstrating biosimilarity to a Reference Product. You will learn about what type and how much clinical data are needed to support a showing of biosimilarity.</description>
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      <title>Election Year Legal and Compliance 2012</title>
      <link>http://www.complianceonline.com/ecommerce/control/trainingFocus?product_id=702228&amp;channel=rss_organic</link>
      <description>This webinar on Federal Campaign Finance Law will assist compliance officers and in-house counsel identify common campaign finance issues faced by corporations and trade associations in major election years.</description>
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