Projekta Nr.ISO/DIS 23494-1
Nosaukums<p class="MsoBodyText" style="mso-layout-grid-align: none; text-autospace: none;"><span lang="EN-GB" style="mso-bidi-font-size: 12.0pt;">This document specifies a general concept for a provenance information model for biological material and data, and requirements for provenance information management.</span></p> <p class="MsoBodyText" style="mso-layout-grid-align: none; text-autospace: none;"><span lang="EN-GB" style="mso-bidi-font-size: 12.0pt;">The provenance information covers any information relevant to the traceability, quality and fitness for purpose of the biological material and data generated throughout the life cycle of the biological material from collection to analysis, including data originating from analytical procedures applied to the biological material and further processing of the data.</span></p> <p class="MsoBodyText" style="mso-layout-grid-align: none; text-autospace: none;"><span lang="EN-GB" style="mso-bidi-font-size: 12.0pt;">This document is applicable to organizations, authorities and industries that are:</span></p> <p class="ListContinue1"><span lang="EN-GB">a)<span style="mso-tab-count: 1;">    </span>collecting, processing or distributing biological material for research; </span></p> <p class="ListContinue1"><span lang="EN-GB">b)<span style="mso-tab-count: 1;">    </span>generating, collecting, analysing or storing data on biological material.</span></p> <p class="MsoBodyText" style="mso-layout-grid-align: none; text-autospace: none;"><span lang="EN-GB" style="mso-bidi-font-size: 12.0pt;">This document does not apply to biological material and data used for medical diagnosis and therapy.</span></p> <p class="Note" style="tab-stops: 19.85pt 39.7pt 48.25pt 59.55pt 79.4pt 99.25pt 119.05pt 138.9pt 158.75pt 178.6pt 7.0cm; mso-layout-grid-align: none; text-autospace: none;"><span lang="EN-GB" style="mso-bidi-font-size: 12.0pt;">NOTE<span style="mso-tab-count: 1;">       </span>International, national, or regional regulations or requirements can also apply to specific topics covered in this document.</span></p>
Reģistrācijas numurs (WIID)89266
Darbības sfēra<p class="MsoBodyText" style="mso-layout-grid-align: none; text-autospace: none;"><span lang="EN-GB" style="mso-bidi-font-size: 12.0pt;">This document specifies a general concept for a provenance information model for biological material and data, and requirements for provenance information management.</span></p> <p class="MsoBodyText" style="mso-layout-grid-align: none; text-autospace: none;"><span lang="EN-GB" style="mso-bidi-font-size: 12.0pt;">The provenance information covers any information relevant to the traceability, quality and fitness for purpose of the biological material and data generated throughout the life cycle of the biological material from collection to analysis, including data originating from analytical procedures applied to the biological material and further processing of the data.</span></p> <p class="MsoBodyText" style="mso-layout-grid-align: none; text-autospace: none;"><span lang="EN-GB" style="mso-bidi-font-size: 12.0pt;">This document is applicable to organizations, authorities and industries that are:</span></p> <p class="ListContinue1"><span lang="EN-GB">a)<span style="mso-tab-count: 1;">    </span>collecting, processing or distributing biological material for research; </span></p> <p class="ListContinue1"><span lang="EN-GB">b)<span style="mso-tab-count: 1;">    </span>generating, collecting, analysing or storing data on biological material.</span></p> <p class="MsoBodyText" style="mso-layout-grid-align: none; text-autospace: none;"><span lang="EN-GB" style="mso-bidi-font-size: 12.0pt;">This document does not apply to biological material and data used for medical diagnosis and therapy.</span></p> <p class="Note" style="tab-stops: 19.85pt 39.7pt 48.25pt 59.55pt 79.4pt 99.25pt 119.05pt 138.9pt 158.75pt 178.6pt 7.0cm; mso-layout-grid-align: none; text-autospace: none;"><span lang="EN-GB" style="mso-bidi-font-size: 12.0pt;">NOTE<span style="mso-tab-count: 1;">       </span>International, national, or regional regulations or requirements can also apply to specific topics covered in this document.</span></p>
StatussIzstrādē
ICS grupa07.080