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| Regulation, Specification, or Guidance
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Requirement
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42 CFR Part 493.1241
ASTM E1578-18 C-1-1
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The system should allow for sample registration prior to (e.g., preregistration) or after (e.g., registration) physical sample collection.
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21 CFR Part 58.105 (c)
21 CFR Part 211.84
21 CFR Part 211.101
21 CFR Part 226.80
21 CFR Part 606.120 (b)
21 CFR Part 606.121 (c–i)
21 CFR Part 606.140 (c)
29 CFR Part 1910.1030 (g)
29 CFR Part 1910.1096 (e1-6)
42 CFR Part 493.1232
ABFT Accreditation Manual Sec. D
ASTM E1492-11 4.1.1.6
ASTM E1578-18 C-1-2
EPA ERLN Laboratory Requirements 3.2.2
EPA QA/G-5 2.2.3
E.U. Commission Directive 2003/94/EC Article 15
OECD GLP Principles 6.1
USDA Sampling Procedures for PDP 6.4.1.2.6
WHO Technical Report Series, #986, Annex 2, 17.11
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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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45 CFR Part 162.410
CJIS Security Policy 5.6.1
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The system shall provide a means to assign unique identifiers such as a National Provider Identifier (NPI) or Originating Agency Identifier (ORI) to the enacting entity and any subcontracted entity. The unique identifier should be able to appear on necessary records, documents, and reports referencing those entities.
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42 CFR Part 493.1241
ASTM E1578-18 C-1-3
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The system should provide a means for automatically registering samples in the system using any number of triggers such as dates, times, web requests, and intra-system methods like APIs and web services.
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ASTM E1578-18 C-1-4
USDA Sampling Procedures for PDP 6.4.1.1.3
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The system should permit metadata like lot number, client demographics, sampling point, random selection process used, and industry-specific items to be included during registration.
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| ASTM E1578-18 C-1-5
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The system shall allow for the addition, modification, and removal of new, pre-defined, and custom analytical tests.
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| ASTM E1578-18 C-1-6
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The system should offer safety information related to a submitted sample upon registration that is relevant to the lab's location and industry.
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| ASTM E1578-18 C-1-7
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The system should support the creation and use of predefined metadata templates, as well as ad-hoc, single, and multiple samples.
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7 CFR Part 331.17
9 CFR Part 121.17
21 CFR Part 58.105 (c)
21 CFR Part 58.195
21 CFR Part 211.84
21 CFR Part 211.170
21 CFR Part 211.194
21 CFR Part 312.57 (d)
40 CFR Part 141.33
42 CFR Part 73.17
42 CFR Part 493.1105
42 CFR Part 493.1241
42 CFR Part 493.1242
42 CFR Part 493.1274 (f)
42 CFR Part 493.1283
AAFCO QA/QC Guidelines for Feed Laboratories Sec. 2.2–3
AAVLD Requirements for an AVMDL Sec. 5.7.1.2
ABFT Accreditation Manual Sec. D
ASTM E1578-18 C-1-8
EPA 815-R-05-004 Chap. IV, Sec. 6 and 8
EPA 815-R-05-004 Chap. VI, Sec. 8
EPA ERLN Laboratory Requirements 3.2
EPA ERLN Laboratory Requirements 4.4.10–11
EPA ERLN Laboratory Requirements 4.7.1–6
EPA QA/G-5 2.2.2 and 2.2.3
E.U. Commission Directive 2003/94/EC Article 11.4
ISO 15189:2012 5.7.2
OECD GLP Principles 6.1
USDA Sample Processing and Analysis Procedures for PDP 5.1 and 5.1.13
USDA Sampling Procedures for PDP 5.1
WHO Technical Report Series, #986, Annex 2, 17.11 and 17.21
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The system shall be able to define the sample collection details for registered samples, including container size and type, number of containers, collection date and time, name of the collector, lot number, storage location, preservation method, collection methods used (standard and nonstandard), safety concerns, and retention period.
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