Template:LIMSpec/Inventory management - Revision history

Shawndouglas: Updated for food and bev update

2022-12-01T21:29:00Z

Updated for food and bev update

← Older revision		Revision as of 21:29, 1 December 2022
Line 37:		Line 37:
	\|-		\|-
	\| style="padding:5px; width:500px;" \|		\| style="padding:5px; width:500px;" \|
			[https://www.law.cornell.edu/cfr/text/21/part-117 21 CFR Part 117.420]<br />
	[https://www.law.cornell.edu/cfr/text/21/212.40 21 CFR Part 212.40 (c)]<br />		[https://www.law.cornell.edu/cfr/text/21/212.40 21 CFR Part 212.40 (c)]<br />
	[https://www.law.cornell.edu/cfr/text/21/820.50 21 CFR Part 820.50]<br />		[https://www.law.cornell.edu/cfr/text/21/820.50 21 CFR Part 820.50]<br />
	[https://www.uslegalforms.com/form-library/256001-c211-specific-checklist-combined-iso-iec-17025-and-veterinary-laboratory-accreditation A2LA C211 4.6]<br />		[https://www.uslegalforms.com/form-library/256001-c211-specific-checklist-combined-iso-iec-17025-and-veterinary-laboratory-accreditation A2LA C211 4.6]<br />
	[https://www.astm.org/e1578-18.html ASTM E1578-18 E-8-4]<br />		[https://www.astm.org/e1578-18.html ASTM E1578-18 E-8-4]<br />
			[https://cdn.scsglobalservices.com/files/program_documents/brc_food_standard_8_0.pdf BRC GSFS, Issue 8, 3.5.1.4]<br />
			[https://www.fao.org/fao-who-codexalimentarius/sh-proxy/en/?lnk=1&url=https%253A%252F%252Fworkspace.fao.org%252Fsites%252Fcodex%252FStandards%252FCXC%2B1-1969%252FCXC_001e.pdf Codex Alimentarius CXC 1-1969, Ch.1, 7.2.8]<br />
			[https://mygfsi.com/news-and-resources/?_keyword=GFSI%20Benchmarking%20Requirements&_type=publications GFSI Benchmarking Rqmts., v2020.1, Part 3, A1, A2, B1, B2, B3, C0, C1, C2, C3, C4, I, K - FSM 13.2.1]<br />
			[https://mygfsi.com/news-and-resources/?_keyword=GFSI%20Benchmarking%20Requirements&_type=publications GFSI Benchmarking Rqmts., v2020.1, Part 3, D - FSM 13.2.2]<br />
			[https://mygfsi.com/news-and-resources/?_keyword=GFSI%20Benchmarking%20Requirements&_type=publications GFSI Benchmarking Rqmts., v2020.1, Part 3, I - FSM 13.2.3]<br />
			[https://mygfsi.com/news-and-resources/?_keyword=GFSI%20Benchmarking%20Requirements&_type=publications GFSI Benchmarking Rqmts., v2020.1, Part 3, A1, A2 - FSM 13.5]<br />
			[https://www.ifs-certification.com/images/standards/ifs_food7/documents/standards/IFS_Food7_en.pdf IFS Food 7, Part 2, 4.4.1]<br />
			[https://www.ifs-certification.com/images/standards/ifs_pacsecure2/documents/standards/IFS_pacsecure2_en.pdf IFS PACsecure 2, Part 2, 4.4.1]<br />
			[https://www.iso.org/standard/44001.html ISO/TS 22002-1:2009, 9.2]<br />
			[https://www.iso.org/standard/60969.html ISO/TS 22002-4:2013, 4.6.2]<br />
			[https://www.iso.org/standard/66126.html ISO/TS 22002-6:2016, 4.6.2]<br />
			[https://www.sqfi.com/wp-content/uploads/2020/11/20227FMIN_FoodManufacturing_v3-2-FINAL-w-links.pdf SQF FSC 9, Food Manufacturing, Part B, 2.3.4.1]<br />
			[https://www.sqfi.com/wp-content/uploads/2020/11/20227FMIN_PetFood_v3-2-Final-w-Links.pdf SQF FSC 9, Pet Food Manufacturing, Part B, 2.3.4.1]<br />
			[https://www.sqfi.com/wp-content/uploads/2020/11/20227FMIN_FoodPackaging_v3-2-Final-w-Links.pdf SQF FSC 9, Manufacture of Food Packaging, Part B, 2.3.4.1]<br />
	[https://ris.dls.virginia.gov/uploads/1VAC30/dibr/Microsoft%20Word%20-%20STD-ELV1-2016-Rev2.1_LabReqs_ANSIapp.doc-20210426142653.pdf TNI EL-V1-2016-Rev.2.1 (V1,M2 4.6.4)]<br />		[https://ris.dls.virginia.gov/uploads/1VAC30/dibr/Microsoft%20Word%20-%20STD-ELV1-2016-Rev2.1_LabReqs_ANSIapp.doc-20210426142653.pdf TNI EL-V1-2016-Rev.2.1 (V1,M2 4.6.4)]<br />
	[https://www.ams.usda.gov/datasets/pdp/pdp-standard-operating-procedures USDA Administrative Procedures for the PDP 7.1]<br />		[https://www.ams.usda.gov/datasets/pdp/pdp-standard-operating-procedures USDA Administrative Procedures for the PDP 7.1]<br />

Shawndouglas: Updated for 2022.

2022-05-05T20:31:44Z

Updated for 2022.

← Older revision		Revision as of 20:31, 5 May 2022
Line 8:		Line 8:
	! style="color:brown; background-color:#ffffee; width:700px;"\| Requirement		! style="color:brown; background-color:#ffffee; width:700px;"\| Requirement
	\|-		\|-
	\| style="padding:5px; width:500px;" \|[https://www.astm.org/~~Standards/E1578~~.~~htm~~ ASTM E1578-18 E-8-1]		\| style="padding:5px; width:500px;" \|[https://www.astm.org/e1578-18.html ASTM E1578-18 E-8-1]<br />[https://elss.cap.org/elss/ShowProperty?nodePath=/UCMCON/Contribution%20Folders/DctmContent/education/OnlineCourseContent/2017/LAP-TLTM/misc/lam.pdf CAP Laboratory Accreditation Manual]<br />[https://www.wadsworth.org/regulatory/clep/clinical-labs/laboratory-standards NYSDOH CLEP Clinical Laboratory Standards of Practice, General Systems Standards]
	\| style="background-color:white;" \|'''15.1''' The system should be capable of accurately tracking the specific quantities of received and consumed test samples.		\| style="background-color:white;" \|'''15.1''' The system should be capable of accurately tracking the specific quantities of received and consumed test samples and specimens.
	\|-		\|-
	\| style="padding:5px; width:500px;" \|[https://www.law.cornell.edu/cfr/text/21/212.60 21 CFR Part 212.60 (d)]<br />[https://www.astm.org/~~Standards/E1578~~.~~htm~~ ASTM E1578-18 E-8-2]		\| style="padding:5px; width:500px;" \|
			[https://www.law.cornell.edu/cfr/text/21/212.60 21 CFR Part 212.60 (d)]<br />
			[https://www.astm.org/e1578-18.html ASTM E1578-18 E-8-2]<br />
			[https://clsi.org/standards/products/quality-management-systems/documents/qms22/ CLSI QMS22 2.1.2]<br />
			[https://www.wadsworth.org/regulatory/clep/clinical-labs/laboratory-standards NYSDOH CLEP Clinical Laboratory Standards of Practice, General Systems Standards]
	\| style="background-color:white;" \|'''15.2''' The system should support the recording of inventory items' attributes, including chemical name, internal name, catalog number, reorder level, consumable or reusable status, and expiration date.		\| style="background-color:white;" \|'''15.2''' The system should support the recording of inventory items' attributes, including chemical name, internal name, catalog number, reorder level, consumable or reusable status, and expiration date.
	\|-		\|-
Line 23:		Line 27:
	[https://www.law.cornell.edu/cfr/text/29/1910.1096 29 CFR Part 1910.1096 (e-6)]<br />		[https://www.law.cornell.edu/cfr/text/29/1910.1096 29 CFR Part 1910.1096 (e-6)]<br />
	[https://www.law.cornell.edu/cfr/text/29/1910.1200 29 CFR Part 1910.1200 (f-6) and (f-10)]<br />		[https://www.law.cornell.edu/cfr/text/29/1910.1200 29 CFR Part 1910.1200 (f-6) and (f-10)]<br />
	[https://www.astm.org/~~Standards/E1578~~.~~htm~~ ASTM E1578-18 E-8-3]<br />		[https://www.law.cornell.edu/cfr/text/40/262.206 40 CFR Part 262.206]<br />
	[https://www.~~who~~.~~int~~/~~medicines~~/~~areas~~/~~quality_safety~~/~~quality_assurance~~/~~expert_committee~~/~~trs_986~~/en/ WHO Technical Report Series, #986, Annex 2, 14.13, 14.35, and 14.41]<br />		[https://www.astm.org/e1578-18.html ASTM E1578-18 E-8-3]<br />
	[https://~~www~~.who.int/medicines/~~areas/quality_safety/quality_assurance/expert_committee/trs_986/en/~~ WHO Technical Report Series, #986, Annex 2, 15.10–12]		[https://www.wadsworth.org/regulatory/clep/clinical-labs/laboratory-standards NYSDOH CLEP Clinical Laboratory Standards of Practice, General Systems Standards]<br />
			[https://www.osha.gov/laws-regs/regulations/standardnumber/1910/1910.1200 OSHA 1910.1200(b)(3) and (f)]<br />
			[https://www.osha.gov/laws-regs/regulations/standardnumber/1910/1910.1450 OSHA 1910.1450(h)]<br />
			[https://extranet.who.int/pqweb/medicines/who-technical-report-series WHO Technical Report Series, #986, Annex 2, 14.13, 14.35, and 14.41]<br />
			[https://extranet.who.int/pqweb/medicines/who-technical-report-series WHO Technical Report Series, #986, Annex 2, 15.10–12]
	\| style="background-color:white;" \|'''15.3''' The system should be capable of designing and printing labels in a variety of sizes, formats, and inventory categories.		\| style="background-color:white;" \|'''15.3''' The system should be capable of designing and printing labels in a variety of sizes, formats, and inventory categories.
	\|-		\|-
Line 31:		Line 39:
	[https://www.law.cornell.edu/cfr/text/21/212.40 21 CFR Part 212.40 (c)]<br />		[https://www.law.cornell.edu/cfr/text/21/212.40 21 CFR Part 212.40 (c)]<br />
	[https://www.law.cornell.edu/cfr/text/21/820.50 21 CFR Part 820.50]<br />		[https://www.law.cornell.edu/cfr/text/21/820.50 21 CFR Part 820.50]<br />
	[https://www.astm.org/~~Standards/E1578~~.~~htm~~ ASTM E1578-18 E-8-4]<br />		[https://www.uslegalforms.com/form-library/256001-c211-specific-checklist-combined-iso-iec-17025-and-veterinary-laboratory-accreditation A2LA C211 4.6]<br />
			[https://www.astm.org/e1578-18.html ASTM E1578-18 E-8-4]<br />
			[https://ris.dls.virginia.gov/uploads/1VAC30/dibr/Microsoft%20Word%20-%20STD-ELV1-2016-Rev2.1_LabReqs_ANSIapp.doc-20210426142653.pdf TNI EL-V1-2016-Rev.2.1 (V1,M2 4.6.4)]<br />
	[https://www.ams.usda.gov/datasets/pdp/pdp-standard-operating-procedures USDA Administrative Procedures for the PDP 7.1]<br />		[https://www.ams.usda.gov/datasets/pdp/pdp-standard-operating-procedures USDA Administrative Procedures for the PDP 7.1]<br />
	[https://~~www~~.who.int/medicines/~~areas~~/~~quality_safety~~/~~quality_assurance~~/~~expert_committee~~/~~trs_986~~/en/ WHO Technical Report Series, #986, Annex 2, 14.8]		[https://extranet.who.int/pqweb/medicines/who-technical-report-series WHO Technical Report Series, #961, Annex 13, 7.1 and 7.3]<br />
			[https://extranet.who.int/pqweb/medicines/who-technical-report-series WHO Technical Report Series, #986, Annex 2, 14.8]
	\| style="background-color:white;" \|'''15.4''' The system should provide a means for ordering inventory through a qualified vendor using a vendor master list containing approval status for order validation.		\| style="background-color:white;" \|'''15.4''' The system should provide a means for ordering inventory through a qualified vendor using a vendor master list containing approval status for order validation.
	\|-		\|-
Line 42:		Line 53:
	[https://www.law.cornell.edu/cfr/text/21/606.165 21 CFR Part 606.165]<br />		[https://www.law.cornell.edu/cfr/text/21/606.165 21 CFR Part 606.165]<br />
	[https://www.law.cornell.edu/cfr/text/29/1910.1450 29 CFR Part 1910.1450 Appendix A (I)]<br />		[https://www.law.cornell.edu/cfr/text/29/1910.1450 29 CFR Part 1910.1450 Appendix A (I)]<br />
	[https://www.astm.org/~~Standards/E1578~~.~~htm~~ ASTM E1578-18 E-8-5]		[https://www.uslegalforms.com/form-library/256001-c211-specific-checklist-combined-iso-iec-17025-and-veterinary-laboratory-accreditation A2LA C211 4.6]<br />
	\| style="background-color:white;" \|'''15.5''' The system should provide a means for accurately recording the receipt, ~~issue~~, distribution, and disposal of materials.		[https://www.astm.org/e1578-18.html ASTM E1578-18 E-8-5]<br />
			[https://www.wadsworth.org/regulatory/clep/clinical-labs/laboratory-standards NYSDOH CLEP Clinical Laboratory Standards of Practice, General Systems Standards]<br />
			[https://ris.dls.virginia.gov/uploads/1VAC30/dibr/Microsoft%20Word%20-%20STD-ELV1-2016-Rev2.1_LabReqs_ANSIapp.doc-20210426142653.pdf TNI EL-V1-2016-Rev.2.1 (V1,M2 4.6.2)]<br />
			[https://www.ams.usda.gov/sites/default/files/media/TestingGuidelinesforHemp.pdf USDA Hemp Production Program Laboratory Testing Guidelines, Summary of Practice 1.5]
			\| style="background-color:white;" \|'''15.5''' The system should provide a means for accurately recording the receipt, approval, distribution, and disposal of materials.
	\|-		\|-
	\| style="padding:5px; width:500px;" \|		\| style="padding:5px; width:500px;" \|
Line 52:		Line 67:
	[https://www.law.cornell.edu/cfr/text/21/211.142 21 CFR Part 211.142 (a)]<br />		[https://www.law.cornell.edu/cfr/text/21/211.142 21 CFR Part 211.142 (a)]<br />
	[https://www.law.cornell.edu/cfr/text/21/212.40 21 CFR Part 212.40 (c)]<br />		[https://www.law.cornell.edu/cfr/text/21/212.40 21 CFR Part 212.40 (c)]<br />
	[https://www.astm.org/~~Standards/E1578~~.~~htm~~ ASTM E1578-18 E-8-6]<br />		[https://www.astm.org/e1578-18.html ASTM E1578-18 E-8-6]<br />
	[https://~~www~~.who.int/medicines/~~areas/quality_safety/quality_assurance/expert_committee/trs_986/en/~~ WHO Technical Report Series, #986, Annex 2, 12.18]		[https://extranet.who.int/pqweb/medicines/who-technical-report-series WHO Technical Report Series, #986, Annex 2, 12.18]
	\| style="background-color:white;" \|'''15.6''' The system should provide a means for quarantining specific material types until they can be validated by a quality control test or disposed of.		\| style="background-color:white;" \|'''15.6''' The system should provide a means for quarantining specific material types until they can be validated by a quality control test or disposed of.
	\|-		\|-
Line 60:		Line 75:
	[https://www.law.cornell.edu/cfr/text/21/211.110 21 CFR Part 211.110 (d)]<br />		[https://www.law.cornell.edu/cfr/text/21/211.110 21 CFR Part 211.110 (d)]<br />
	[https://www.law.cornell.edu/cfr/text/42/493.1252 42 CFR Part 493.1252 (d)]<br />		[https://www.law.cornell.edu/cfr/text/42/493.1252 42 CFR Part 493.1252 (d)]<br />
	[https://www.astm.org/~~Standards/E1578~~.~~htm~~ ASTM E1578-18 E-8-7]		[https://www.astm.org/e1578-18.html ASTM E1578-18 E-8-7]
	\| style="background-color:white;" \|'''15.7''' The system should allow authorized personnel to retire faulty or poor quality materials from use.		\| style="background-color:white;" \|'''15.7''' The system should allow authorized personnel to retire faulty or poor quality materials from use.
	\|-		\|-
	\| style="padding:5px; width:500px;" \|		\| style="padding:5px; width:500px;" \|
	[https://www.law.cornell.edu/cfr/text/21/211.89 21 CFR Part 211.89]<br />[https://www.astm.org/~~Standards/E1578~~.~~htm~~ ASTM E1578-18 E-8-8]		[https://www.law.cornell.edu/cfr/text/21/211.89 21 CFR Part 211.89]<br />[https://www.astm.org/e1578-18.html ASTM E1578-18 E-8-8]
	\| style="background-color:white;" \|'''15.8''' The system shall clearly designate a standard or reagent as being disposed or consumed.		\| style="background-color:white;" \|'''15.8''' The system shall clearly designate a standard or reagent as being disposed or consumed.
	\|-		\|-
	\|}		\|}
	\|}		\|}

Shawndouglas: Fixed broken URLs

2021-01-27T21:12:52Z

Fixed broken URLs

Shawndouglas: Created as needed.

2019-09-19T22:42:39Z

Created as needed.

New page

{|
| STYLE="vertical-align:top;"|
{| class="wikitable collapsible" border="1" cellpadding="10" cellspacing="0"
|-
! colspan="2" style="text-align:left; padding-left:20px; padding-top:10px; padding-bottom:10px;"|
|-
! style="color:brown; background-color:#ffffee; width:500px;"| Regulation, Specification, or Guidance
! style="color:brown; background-color:#ffffee; width:700px;"| Requirement
|-
| style="padding:5px; width:500px;" |[https://www.astm.org/Standards/E1578.htm ASTM E1578-18 E-8-1]
| style="background-color:white;" |'''15.1''' The system should be capable of accurately tracking the specific quantities of received and consumed test samples.
|-
| style="padding:5px; width:500px;" |[https://www.law.cornell.edu/cfr/text/21/212.60 21 CFR Part 212.60 (d)] [https://www.astm.org/Standards/E1578.htm ASTM E1578-18 E-8-2]
| style="background-color:white;" |'''15.2''' The system should support the recording of inventory items' attributes, including chemical name, internal name, catalog number, reorder level, consumable or reusable status, and expiration date.
|-
| style="padding:5px; width:500px;" |
[https://www.law.cornell.edu/cfr/text/21/211.84 21 CFR Part 211.84] 
[https://www.law.cornell.edu/cfr/text/21/211.101 21 CFR Part 211.101] 
[https://www.law.cornell.edu/cfr/text/21/212.60 21 CFR Part 212.60 (d)] 
[https://www.law.cornell.edu/cfr/text/21/226.80 21 CFR Part 226.80] 
[https://www.law.cornell.edu/cfr/text/21/606.120 21 CFR Part 606.120 (b)] 
[https://www.law.cornell.edu/cfr/text/29/1910.1030 29 CFR Part 1910.1030 (g)] 
[https://www.law.cornell.edu/cfr/text/29/1910.1096 29 CFR Part 1910.1096 (e-6)] 
[https://www.law.cornell.edu/cfr/text/29/1910.1200 29 CFR Part 1910.1200 (f-6) and (f-10)] 
[https://www.astm.org/Standards/E1578.htm ASTM E1578-18 E-8-3] 
[https://extranet.who.int/prequal/content/who-technical-report-series WHO Technical Report Series, #986, Annex 2, 14.13, 14.35, and 14.41] 
[https://extranet.who.int/prequal/content/who-technical-report-series WHO Technical Report Series, #986, Annex 2, 15.10–12]
| style="background-color:white;" |'''15.3''' The system should be capable of designing and printing labels in a variety of sizes, formats, and inventory categories.
|-
| style="padding:5px; width:500px;" |
[https://www.law.cornell.edu/cfr/text/21/212.40 21 CFR Part 212.40 (c)] 
[https://www.law.cornell.edu/cfr/text/21/820.50 21 CFR Part 820.50] 
[https://www.astm.org/Standards/E1578.htm ASTM E1578-18 E-8-4] 
[https://www.ams.usda.gov/datasets/pdp/pdp-standard-operating-procedures USDA Administrative Procedures for the PDP 7.1] 
[https://extranet.who.int/prequal/content/who-technical-report-series WHO Technical Report Series, #986, Annex 2, 14.8]
| style="background-color:white;" |'''15.4''' The system should provide a means for ordering inventory through a qualified vendor using a vendor master list containing approval status for order validation.
|-
| style="padding:5px; width:500px;" |
[https://www.law.cornell.edu/cfr/text/21/211.196 21 CFR Part 211.196] 
[https://www.law.cornell.edu/cfr/text/21/212.90 21 CFR Part 212.90] 
[https://www.law.cornell.edu/cfr/text/21/225.110 21 CFR Part 225.110] 
[https://www.law.cornell.edu/cfr/text/21/606.165 21 CFR Part 606.165] 
[https://www.law.cornell.edu/cfr/text/29/1910.1450 29 CFR Part 1910.1450 Appendix A (I)]
[https://www.astm.org/Standards/E1578.htm ASTM E1578-18 E-8-5] 
| style="background-color:white;" |'''15.5''' The system should provide a means for accurately recording the receipt, issue, distribution, and disposal of materials.
|-
| style="padding:5px; width:500px;" |
[https://www.law.cornell.edu/cfr/text/21/211.82 21 CFR Part 211.82 (b)] 
[https://www.law.cornell.edu/cfr/text/21/211.84 21 CFR Part 211.84 (a)] 
[https://www.law.cornell.edu/cfr/text/21/211.89 21 CFR Part 211.89] 
[https://www.law.cornell.edu/cfr/text/21/211.110 21 CFR Part 211.110 (d)] 
[https://www.law.cornell.edu/cfr/text/21/211.142 21 CFR Part 211.142 (a)] 
[https://www.law.cornell.edu/cfr/text/21/212.40 21 CFR Part 212.40 (c)] 
[https://www.astm.org/Standards/E1578.htm ASTM E1578-18 E-8-6] 
[https://extranet.who.int/prequal/content/who-technical-report-series WHO Technical Report Series, #986, Annex 2, 12.18]
| style="background-color:white;" |'''15.6''' The system should provide a means for quarantining specific material types until they can be validated by a quality control test or disposed of.
|-
| style="padding:5px; width:500px;" |
[https://www.law.cornell.edu/cfr/text/21/211.89 21 CFR Part 211.89] 
[https://www.law.cornell.edu/cfr/text/21/211.110 21 CFR Part 211.110 (d)] 
[https://www.law.cornell.edu/cfr/text/42/493.1252 42 CFR Part 493.1252 (d)] 
[https://www.astm.org/Standards/E1578.htm ASTM E1578-18 E-8-7]
| style="background-color:white;" |'''15.7''' The system should allow authorized personnel to retire faulty or poor quality materials from use.
|-
| style="padding:5px; width:500px;" |
[https://www.law.cornell.edu/cfr/text/21/211.89 21 CFR Part 211.89] [https://www.astm.org/Standards/E1578.htm ASTM E1578-18 E-8-8]
| style="background-color:white;" |'''15.8''' The system shall clearly designate a standard or reagent as being disposed or consumed.
|-
|}
|}

← Older revision		Revision as of 21:12, 27 January 2021
Line 24:		Line 24:
	[https://www.law.cornell.edu/cfr/text/29/1910.1200 29 CFR Part 1910.1200 (f-6) and (f-10)]<br />		[https://www.law.cornell.edu/cfr/text/29/1910.1200 29 CFR Part 1910.1200 (f-6) and (f-10)]<br />
	[https://www.astm.org/Standards/E1578.htm ASTM E1578-18 E-8-3]<br />		[https://www.astm.org/Standards/E1578.htm ASTM E1578-18 E-8-3]<br />
	[https://~~extranet~~.who.int/~~prequal~~/~~content~~/~~who-technical-report-series~~ WHO Technical Report Series, #986, Annex 2, 14.13, 14.35, and 14.41]<br />		[https://www.who.int/medicines/areas/quality_safety/quality_assurance/expert_committee/trs_986/en/ WHO Technical Report Series, #986, Annex 2, 14.13, 14.35, and 14.41]<br />
	[https://~~extranet~~.who.int/~~prequal~~/~~content~~/~~who-technical-report-series~~ WHO Technical Report Series, #986, Annex 2, 15.10–12]		[https://www.who.int/medicines/areas/quality_safety/quality_assurance/expert_committee/trs_986/en/ WHO Technical Report Series, #986, Annex 2, 15.10–12]
	\| style="background-color:white;" \|'''15.3''' The system should be capable of designing and printing labels in a variety of sizes, formats, and inventory categories.		\| style="background-color:white;" \|'''15.3''' The system should be capable of designing and printing labels in a variety of sizes, formats, and inventory categories.
	\|-		\|-
Line 33:		Line 33:
	[https://www.astm.org/Standards/E1578.htm ASTM E1578-18 E-8-4]<br />		[https://www.astm.org/Standards/E1578.htm ASTM E1578-18 E-8-4]<br />
	[https://www.ams.usda.gov/datasets/pdp/pdp-standard-operating-procedures USDA Administrative Procedures for the PDP 7.1]<br />		[https://www.ams.usda.gov/datasets/pdp/pdp-standard-operating-procedures USDA Administrative Procedures for the PDP 7.1]<br />
	[https://~~extranet~~.who.int/~~prequal~~/~~content~~/~~who-technical-report-series~~ WHO Technical Report Series, #986, Annex 2, 14.8]		[https://www.who.int/medicines/areas/quality_safety/quality_assurance/expert_committee/trs_986/en/ WHO Technical Report Series, #986, Annex 2, 14.8]
	\| style="background-color:white;" \|'''15.4''' The system should provide a means for ordering inventory through a qualified vendor using a vendor master list containing approval status for order validation.		\| style="background-color:white;" \|'''15.4''' The system should provide a means for ordering inventory through a qualified vendor using a vendor master list containing approval status for order validation.
	\|-		\|-
Line 41:		Line 41:
	[https://www.law.cornell.edu/cfr/text/21/225.110 21 CFR Part 225.110]<br />		[https://www.law.cornell.edu/cfr/text/21/225.110 21 CFR Part 225.110]<br />
	[https://www.law.cornell.edu/cfr/text/21/606.165 21 CFR Part 606.165]<br />		[https://www.law.cornell.edu/cfr/text/21/606.165 21 CFR Part 606.165]<br />
	[https://www.law.cornell.edu/cfr/text/29/1910.1450 29 CFR Part 1910.1450 Appendix A (I)]		[https://www.law.cornell.edu/cfr/text/29/1910.1450 29 CFR Part 1910.1450 Appendix A (I)]<br />
	[https://www.astm.org/Standards/E1578.htm ASTM E1578-18 E-8-5]~~<br />~~		[https://www.astm.org/Standards/E1578.htm ASTM E1578-18 E-8-5]
	\| style="background-color:white;" \|'''15.5''' The system should provide a means for accurately recording the receipt, issue, distribution, and disposal of materials.		\| style="background-color:white;" \|'''15.5''' The system should provide a means for accurately recording the receipt, issue, distribution, and disposal of materials.
	\|-		\|-
Line 53:		Line 53:
	[https://www.law.cornell.edu/cfr/text/21/212.40 21 CFR Part 212.40 (c)]<br />		[https://www.law.cornell.edu/cfr/text/21/212.40 21 CFR Part 212.40 (c)]<br />
	[https://www.astm.org/Standards/E1578.htm ASTM E1578-18 E-8-6]<br />		[https://www.astm.org/Standards/E1578.htm ASTM E1578-18 E-8-6]<br />
	[https://~~extranet~~.who.int/~~prequal~~/~~content~~/~~who-technical-report-series~~ WHO Technical Report Series, #986, Annex 2, 12.18]		[https://www.who.int/medicines/areas/quality_safety/quality_assurance/expert_committee/trs_986/en/ WHO Technical Report Series, #986, Annex 2, 12.18]
	\| style="background-color:white;" \|'''15.6''' The system should provide a means for quarantining specific material types until they can be validated by a quality control test or disposed of.		\| style="background-color:white;" \|'''15.6''' The system should provide a means for quarantining specific material types until they can be validated by a quality control test or disposed of.
	\|-		\|-