Difference between revisions of "User:Shawndouglas/sandbox/sublevel8"
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==Sandbox begins below== | ==Sandbox begins below== | ||
==1.1 Vendor services== | |||
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! colspan="2" style="text-align:left; padding-left:20px; padding-top:10px; padding-bottom:10px;"| 1.1 '''Sample/Experiment Registration''' | |||
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! style="color:brown; background-color:#ffffee; width:500px;"| Regulation, Specification, or Guidance | |||
! style="color:brown; background-color:#ffffee; width:700px;"| Requirement | |||
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| style="padding:5px; width:500px;" |[https://www.law.cornell.edu/cfr/text/42/493.1241 42 CFR Part 493.1241]<br />[https://www.astm.org/Standards/E1578.htm ASTM E1578-18 C-1-1] | |||
| style="background-color:white;" |The system should allow for sample registration prior to (e.g., preregistration) or after (e.g., registration) physical sample collection. | |||
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| style="padding:5px; width:500px;" |[https://www.law.cornell.edu/cfr/text/21/58.105 21 CFR Part 58.105 (c)]<br />[https://www.law.cornell.edu/cfr/text/21/211.84 21 CFR Part 211.84]<br />[https://www.law.cornell.edu/cfr/text/21/211.101 21 CFR Part 211.101]<br />[https://www.law.cornell.edu/cfr/text/21/226.80 21 CFR Part 226.80]<br />[https://www.law.cornell.edu/cfr/text/21/606.120 21 CFR Part 606.120 (b)]<br />[https://www.law.cornell.edu/cfr/text/21/606.121 21 CFR Part 606.121 (c–i)]<br />[https://www.law.cornell.edu/cfr/text/21/606.140 21 CFR Part 606.140 (c)]<br />[https://www.law.cornell.edu/cfr/text/29/1910.1030 29 CFR Part 1910.1030 (g)]<br />[https://www.law.cornell.edu/cfr/text/29/1910.1096 29 CFR Part 1910.1096 (e1-6)]<br /> | |||
[https://www.law.cornell.edu/cfr/text/42/493.1232 42 CFR Part 493.1232]<br />[http://www.abft.org/files/ABFT_LAP_Standards_May_31_2013.pdf ABFT Accreditation Manual Sec. D]<br />[https://www.astm.org/Standards/E1492.htm ASTM E1492-11 4.1.1.6]<br />[https://www.astm.org/Standards/E1578.htm ASTM E1578-18 C-1-2]<br />[https://www.epa.gov/sites/production/files/documents/erln_lab_requirements.pdf EPA ERLN Laboratory Requirements 3.2.2]<br />[https://www.epa.gov/quality/guidance-quality-assurance-project-plans-epa-qag-5 EPA QA/G-5 2.2.3]<br />[https://ec.europa.eu/health/sites/health/files/files/eudralex/vol-1/dir_2003_94/dir_2003_94_en.pdf E.U. Commission Directive 2003/94/EC Article 15]<br />[http://www.oecd.org/chemicalsafety/testing/oecdseriesonprinciplesofgoodlaboratorypracticeglpandcompliancemonitoring.htm OECD GLP Principles 6.1]<br />[https://www.ams.usda.gov/datasets/pdp/pdp-standard-operating-procedures USDA Sampling Procedures for PDP 6.4.1.2.6]<br />[https://extranet.who.int/prequal/content/who-technical-report-series WHO Technical Report Series, #986, Annex 2, 17.11] | |||
| style="background-color:white;" |The system should allow for creation and use of pre-configured (e.g., for basic clinical samples) and customizable (e.g., for regulated activities such as blood collection and storage) sample labels, with barcode support. | |||
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Revision as of 15:44, 13 September 2019
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This is sublevel1 of my sandbox, where I play with features and test MediaWiki code. If you wish to leave a comment for me, please see my discussion page instead. |
Sandbox begins below
1.1 Vendor services
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