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| Regulation, Specification, or Guidance
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Requirement
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▪ 21 CFR Part 1.1149
▪ 42 CFR Part 493.1241
▪ APHL 2019 LIS Project Management Guidebook
▪ ASTM E1578-18 C-1-1
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1.1 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
▪ APHL 2019 LIS Project Management Guidebook
▪ ASTM E1492-11 4.1.1.6
▪ ASTM E1578-18 C-1-2
▪ CLSI QMS22 2.2.1.2
▪ 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
▪ TNI EL-V1-2016-Rev.2.1 (V1,M2 5.8.6)
▪ USDA Sampling Procedures for PDP 6.4.1.2.6
▪ WHO Technical Report Series, #986, Annex 2, 17.11
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1.2 The system should allow for creation and use of pre-configured (e.g., for standard inflorescence) and customizable (e.g., for differing substrate/matrix) sample labels, with barcode support.
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▪ 45 CFR Part 162.410
▪ CJIS Security Policy 5.6.1
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1.3 The system shall provide a means to assign unique identifiers such as a U.S. Department of Food and Agriculture unique cultivator identifier 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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1.4 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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▪ 7 CFR Part 91.19
▪ 21 CFR Part 1.1152 (a–b)
▪ 40 CFR Part 262.18
▪ ACMG Technical Standards for Clinical Genetics Laboratories C2.1
▪ APHL 2019 LIS Project Management Guidebook
▪ ASTM E1578-18 C-1-4
▪ USDA Sampling Procedures for PDP 6.4.1.1.3
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1.5 The system should permit metadata like lot number, field number, client demographics, sampling point, random selection process used, and other cannabis-specific identifiers to be included during registration.
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| ▪ ASTM E1578-18 C-1-5
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1.6 The system shall allow for the addition, modification, and removal of new, pre-defined, and custom cannabis-related analytical tests and test protocols—with configurable measurement units and substrates/matrices—while preferably coming pre-loaded with common state- and local-compliant cannabis testing protocols. These protocols should include testing for acid and neutral forms of cannabinoids, potency testing, strain identification, water activity, moisture content, pesticides, solvents, heavy metals, microbiological contaminates, fungi, mycotoxins, and foreign matter.
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| ▪ ASTM E1578-18 C-1-6
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1.7 The system, when applicable, should offer safety information related to a submitted cannabis-related sample upon registration, which is relevant to the lab's location and sample type.
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| ▪ ASTM E1578-18 C-1-7
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1.8 The system should support the creation, use, and configuration of predefined metadata templates, capturing metadata mandated by state and local laws and regulations for various cannabis substrates/matrices and derivative products, as well as any other ad-hoc, single, and multiple samples.
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▪ 7 CFR Part 91.19
▪ 7 CFR Part 331.17
▪ 9 CFR Part 121.17
▪ 21 CFR Part 1.1149
▪ 21 CFR Part 1.1152 (a–b)
▪ 21 CFR Part 1.1152 (d)
▪ 21 CFR Part 58.105 (c)
▪ 21 CFR Part 58.195
▪ 21 CFR Part 129.80 (g)
▪ 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
▪ ACMG Technical Standards for Clinical Genetics Laboratories C2
▪ ASTM E1578-18 C-1-8
▪ CLSI QMS22 2.2.1.3
▪ EPA 815-R-05-004 Chap. IV, Sec. 6 and 8
▪ EPA 815-R-05-004 Chap. VI, Sec. 8
▪ EPA 815-R-05-004 Supplement 1
▪ 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
▪ ISO/IEC 17025:2017 7.3.3
▪ NYSDOH CLEP Clinical Laboratory Standards of Practice, General Systems Standards
▪ OECD GLP Principles 6.1
▪ PFP Human and Animal Food Testing Laboratories Best Practices Manual
▪ TNI EL-V1-2016-Rev.2.1 (V1,M2 5.8.6)
▪ 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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1.9 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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▪ ASTM E1578-18 C-1-9
▪ ACMG Technical Standards for Clinical Genetics Laboratories G1.4
▪ CLSI QMS22 2.2.1.3
▪ EPA ERLN Laboratory Requirements 3.2.1
▪ EPA ERLN Laboratory Requirements 4.4.5
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1.10 The system should allow for the addition of observations and descriptions to registered samples in the form of free text.
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| ▪ ASTM E1578-18 C-1-10
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1.11 The system should support the creation of user-definable default sample registration preferences and/or input screens—including associated measurement units and any other regulation-mandated attributes—based upon the various cannabis substrates/matrices and derivative products tested, as well as the sample source location and/or laboratory location.
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▪ 21 CFR Part 1.1149
▪ ASTM E1578-18 C-1-11
▪ PFP Human and Animal Food Testing Laboratories Best Practices Manual
▪ TNI EL-V1-2016-Rev.2.1 (V1,M2 5.8.7)
▪ WADA International Standard for Laboratories (ISL) 5.3.2
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1.12 The system should allow for the manual or automated recording of sample shipping details such as deliverer, location, shipper sample/batch/lot ID, laboratory sample/batch/lot ID, shipper ID, included documentation, and relevant dates and times for both preregistered and post-analysis samples and batches, for chain-of-custody tracking purposes.
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▪ 21 CFR Part 1.1152 (d)
▪ 21 CFR Part 58.107 (c)
▪ 21 CFR Part 211.194
▪ 42 CFR Part 493.1241
▪ 42 CFR Part 493.1274
▪ 42 CFR Part 493.1283
▪ AAVLD Requirements for an AVMDL Sec. 5.8.2
▪ ABFT Accreditation Manual D-3
▪ ASTM E1578-18 C-1-12
▪ CAP Laboratory Accreditation Manual
▪ EPA ERLN Laboratory Requirements 3.2.2
▪ EPA ERLN Laboratory Requirements 4.1.11
▪ EPA ERLN Laboratory Requirements 4.4.10
▪ EPA QA/G-5 2.2.3
▪ E.U. Commission Directive 2003/94/EC Article 15
▪ ISO/IEC 17025:2017 7.4.2
▪ OECD GLP Principles 6.2
▪ PFP Human and Animal Food Testing Laboratories Best Practices Manual
▪ TNI EL-V1-2016-Rev.2.1 (V1,M2 5.8.5)
▪ USDA Sample Processing and Analysis Procedures for PDP 5.1.11
▪ USDA Sampling Procedures for PDP 6.4.1.2.5
▪ WADA International Standard for Laboratories (ISL) 5.3.2
▪ WHO Technical Report Series, #986, Annex 2, 17.11
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1.13 The system shall assign each sample registered in the system a unique identifier using methodologies such as an ID with an incrementing integer or a user-defined naming format.
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▪ 7 CFR Part 331.17
▪ 9 CFR Part 121.17
▪ 21 CFR Part 58.107 (d)
▪ 21 CFR Part 211.194
▪ 42 CFR Part 73.17
▪ ASTM E1578-18 C-1-13
▪ CAP Laboratory Accreditation Manual
▪ CLSI QMS22 2.2.1.3
▪ EPA ERLN Laboratory Requirements 4.4.7
▪ EPA QA/G-5 2.2.3
▪ OECD GLP Principles 6.1
▪ TNI EL-V1-2016-Rev.2.1 (V1,M2 5.8.3)
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1.14 The system shall provide a user-friendly means for acknowledging the physical reception of sample material in the laboratory, including date and time of reception.
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▪ 21 CFR Part 1.1149
▪ ASTM E1578-18 C-1-14
▪ EPA ERLN Laboratory Requirements 4.4.6
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1.15 The system shall allow for the comparison of received samples to the sampling requirements of the customer or laboratory in order to identify variances from those requirements.
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▪ ACMG Technical Standards for Clinical Genetics Laboratories C3.3
▪ AAVLD Requirements for an AVMDL Sec. 5.8.3
▪ ASTM E1492-11 4.1.1.5
▪ ASTM E1492-11 4.1.6
▪ ASTM E1492-11 4.3.3.2
▪ ASTM E1578-18 C-1-15
▪ CAP Laboratory Accreditation Manual
▪ CLSI QMS22 2.2.1.3
▪ EPA ERLN Laboratory Requirements 4.4.13
▪ EPA ERLN Laboratory Requirements 4.11.8
▪ ISO/IEC 17025:2017 7.4.3
▪ NYSDOH CLEP Clinical Laboratory Standards of Practice, General Systems Standards
▪ PFP Human and Animal Food Testing Laboratories Best Practices Manual
▪ TNI EL-V1-2016-Rev.2.1 (V1,M2 5.8.7.2)
▪ USDA Sample Processing and Analysis Procedures for PDP 5.1.3–7
▪ USDA Sampling Procedures for PDP 6.4.1.1.9
▪ WADA International Standard for Laboratories (ISL) 5.3.2 and 5.3.3.1
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1.16 The system should provide a means to document any undesirable or unexpected characteristics of a submitted sample.
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▪ 21 CFR Part 1.1149
▪ A2LA C211 5.7
▪ ASTM E1578-18 C-1-16
▪ EPA QA/G-5 2.2.2 and 2.2.3
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1.17 The system should provide a means to document and associate sample preparation activities such as grinding, homogenization, extraction, filtration, and evaporation with a given sample, batch, method, protocol, etc.
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▪ 7 CFR Part 331.11
▪ 7 CFR Part 331.17
▪ 9 CFR Part 121.11
▪ 9 CFR Part 121.17
▪ 21 CFR Part 1.1149
▪ 21 CFR Part 1.1152 (d)
▪ 42 CFR Part 73.11
▪ 42 CFR Part 73.17
▪ 42 CFR Part 493.1274
▪ A2LA C223 4.13
▪ A2LA C223 5.8
▪ ABFT Accreditation Manual Sec. D-9–10
▪ ASCLD/LAB Supp. Reqs. for the Accreditation of Forensic Science Testing Laboratories 5.8.1.1
▪ ASTM E1578-18 C-1-17
▪ CLSI QMS22 2.2.3.5
▪ EPA 815-R-05-004 Chap. III, Sec. 12
▪ EPA 815-R-05-004 Appendix A
▪ EPA ERLN Laboratory Requirements 3.2.3–5
▪ EPA ERLN Laboratory Requirements 4.1.13
▪ EPA ERLN Laboratory Requirements 4.4.8–9
▪ EPA QA/G-5 2.2.3
▪ GFSI Benchmarking Rqmts., v2020.1, Part 3, A1, A2, B1, B2, B3, C0, C1, C2, C3, C4, I, K - FSM 14.1.1
▪ GFSI Benchmarking Rqmts., v2020.1, Part 3, D - FSM 14.1.2
▪ GFSI Benchmarking Rqmts., v2020.1, Part 3, I - FSM 14.1.3
▪ NIST 800-53, Rev. 5, AU-10(3)
▪ PFP Human and Animal Food Testing Laboratories Best Practices Manual
▪ SQF FSC 9, Food Manufacturing, Part B, 2.6.2
▪ SQF FSC 9, Pet Food Manufacturing, Part B, 2.6.2
▪ SQF FSC 9, Manufacture of Food Packaging, Part B, 2.6.2
▪ TNI EL-V1-2016-Rev.2.1 (V1,M2 5.8.7.5 and 5.8.8)
▪ WADA International Standard for Laboratories (ISL) (throughout)
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1.18 The system shall have the ability to maintain the chain of custody of every sample, meaning the recording of every single sample distribution step to personnel—including details such as unique identifier, name, location, date, and time—while the sample is in the laboratory’s possession.
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▪ 7 CFR Part 331.16
▪ 9 CFR Part 121.16
▪ 42 CFR Part 73.16
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1.19 In the case of regulated samples such as cannabis, the system shall also allow for the recording of transfers to other entities outside the laboratory, including details such as personnel involved, their certification numbers (if applicable), dates, times, and any other required shipping information.
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▪ ACMG Technical Standards for Clinical Genetics Laboratories G1.1
▪ APHL 2019 LIS Project Management Guidebook
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1.20 The system shall be able to link various records together based on a record's metadata, including shipper sample/batch/lot ID, laboratory sample/batch/lot ID, customer, and more.
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