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      <title>QA Lesson Three by Sam Collier</title>
      <link>https://padlet.com/samcolc9/tlk04t2js6eh9xqu</link>
      <description>Sam, Percy, and Seraphin</description>
      <language>en-us</language>
      <pubDate>2023-08-01 23:38:03 UTC</pubDate>
      <lastBuildDate>2026-03-11 18:31:33 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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         <title>NZS ISO 17025</title>
         <author>samcolc9</author>
         <link>https://padlet.com/samcolc9/tlk04t2js6eh9xqu/wish/2654411300</link>
         <description><![CDATA[<div>This is a document outlining several methods used in laboratories for the testing of products and calibration of equipment. Laboratories must complete each section of this document, as this will create methods to follow for quality assurance and management within the laboratory that all personnel within the lab must follow. There must be processes outlined for Resources, Processes, and the Management System.</div>]]></description>
         <enclosure url="" />
         <pubDate>2023-08-01 23:43:41 UTC</pubDate>
         <guid>https://padlet.com/samcolc9/tlk04t2js6eh9xqu/wish/2654411300</guid>
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      <item>
         <title>AS/NZS ISO 9001</title>
         <author>samcolc9</author>
         <link>https://padlet.com/samcolc9/tlk04t2js6eh9xqu/wish/2654412538</link>
         <description><![CDATA[<div>This is a document outlining quality assurance and control processes in all AU/NZ businesses that produce a product. It outlines all quality assurance and control methods within the business, ranging from management to production line. This includes the control of business intelligence, the use of resources within the company, training and support processes within the company, etc.</div>]]></description>
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         <pubDate>2023-08-01 23:47:15 UTC</pubDate>
         <guid>https://padlet.com/samcolc9/tlk04t2js6eh9xqu/wish/2654412538</guid>
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         <title>Sections</title>
         <author>samcolc9</author>
         <link>https://padlet.com/samcolc9/tlk04t2js6eh9xqu/wish/2654438688</link>
         <description><![CDATA[<div>General Requirements<br>- Impartiality<br>- Confidentiality<br><br>Structural Requirements<br>- Legal Identity<br>- Responsibilities<br>- Activities<br>- Management Structure<br>- Procedure Documentation<br>- Management System Control Personnel<br><br>Resource Requirements<br>- Personnel<br>- Facilities<br>- Equipment<br>- Traceability<br>- External Resource Management<br><br>Process Requirements<br>- Reviews<br>- Method Selection, Verification, and Validation<br>- Sampling<br>- Handling<br>- Technical Records<br>- Evaluation of Measurement Uncertainty<br>- Validity Assurance<br>- Result Reports<br>- Calibration Certificates<br>- Sampling Reports<br>- Conformity Reports<br>- Personal Reports (Opinions and Interpretations)<br>- Amendment Handling<br>- Complaint Handling<br>- Non Conformity Procedures<br>- Data Control<br><br>Management System Requirements<br>- Can follow 9001 if Management System is outlined<br>Otherwise:<br>- Documentation<br>- Document Control<br>- Record Control<br>- Risk and Opportunity Actions<br>- Continuous Improvement<br>- Corrective Actions<br>- Internal Audits<br>- Management Review</div>]]></description>
         <enclosure url="" />
         <pubDate>2023-08-02 00:39:05 UTC</pubDate>
         <guid>https://padlet.com/samcolc9/tlk04t2js6eh9xqu/wish/2654438688</guid>
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      <item>
         <title>Sections</title>
         <author>samcolc9</author>
         <link>https://padlet.com/samcolc9/tlk04t2js6eh9xqu/wish/2654452615</link>
         <description><![CDATA[<div>Organizational Context<br>- Outline Organization<br>- Client Needs/Expectations<br>- Scope of QMS<br>- QMS and Processes<br><br>Leadership<br>- General<br>- Customer Focus<br>- Quality Policy Creation<br>- Quality Policy Communication<br>- Roles and Responsibilities<br><br>Planning<br>- Risks and Opportunities Action<br>- Quality Objectives and Achievement Plans<br>- Planning for Changes<br><br>Support<br>- Resources<br>- Competence<br>- Awareness<br>- Communication<br>- Control of Organizational Intelligence<br><br>Operation<br>- Operational Planning and Control<br>- Product Requirements and Guidelines<br>- Product Design and Development Processes<br>- External Resource Control<br>- Production and Service Provisions<br>- Product and Service Release Processes<br>- Control of Non Conforming Output<br><br>Performance Evaluation</div>]]></description>
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         <pubDate>2023-08-02 01:04:44 UTC</pubDate>
         <guid>https://padlet.com/samcolc9/tlk04t2js6eh9xqu/wish/2654452615</guid>
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      <item>
         <title>Similar Amendments</title>
         <author>samcolc9</author>
         <link>https://padlet.com/samcolc9/tlk04t2js6eh9xqu/wish/2654499101</link>
         <description><![CDATA[<div>17025 Section 6 -&gt; 9001 Section 7.1<br>17025 Sections 5.2, 5.5, 5.6, and 5.7 -&gt; 9001 Section 5.3<br>17025 Section 6.5 -&gt; 9001 Section 8.5.2</div>]]></description>
         <enclosure url="" />
         <pubDate>2023-08-02 02:18:18 UTC</pubDate>
         <guid>https://padlet.com/samcolc9/tlk04t2js6eh9xqu/wish/2654499101</guid>
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         <title></title>
         <author>gvgvz7596y</author>
         <link>https://padlet.com/samcolc9/tlk04t2js6eh9xqu/wish/2658298066</link>
         <description><![CDATA[<div>The 9001 is for Quality management systems—Requirements, it can be used for any produce or service product. The 17025 is for General requirements for the competence of testing and calibration laboratories. It also has some quality control procedure but it places more emphasis on labor.</div>]]></description>
         <enclosure url="" />
         <pubDate>2023-08-08 22:34:17 UTC</pubDate>
         <guid>https://padlet.com/samcolc9/tlk04t2js6eh9xqu/wish/2658298066</guid>
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