User:Shawndouglas/sandbox/sublevel12

8. Resource Management

Regulation, Specification, or Guidance Requirement 29 CFR Part 1910.120 29 CFR Part 1910.134 (m) 29 CFR Part 1910.1030 (h-1) 29 CFR Part 1910.1450 (j) CJIS Security Policy 5.2.3 EPA ERLN Laboratory Requirements 4.2.4.1 EPA QA/G-5 2.1.8 USDA Administrative Procedures for the PDP 6.1 USDA Sampling Procedures for PDP 6.1.2.8 and 6.1.3 The system shall have the ability to create and maintain individual personnel records for tracking such things as demographics, certifications, training, evaluations, medical history, and occupational exposure. 21 CFR Part 820.198 42 CFR Part 493.1233 E.U. Commission Directive 2003/94/EC Article 13 WHO Technical Report Series, #986, Annex 2, 2.1 (j) WHO Technical Report Series, #986, Annex 2, 5.0 The system shall allow authorized personnel to document complaints and problems reported to the laboratory or production facility. 7 CFR Part 331.15 9 CFR Part 121.15 21 CFR Part 211.25 29 CFR Part 1910.1450 (f) 42 CFR Part 73.15 ASCLD/LAB Supp. Reqs. for the Accreditation of Forensic Science Testing Laboratories 5.9.3.3 ASTM E1578-18 E-1-1 CJIS Security Policy 5.2.1 EPA ERLN Laboratory Requirements 4.2.4.1 FDA Hazard Analysis Critical Control Point Guidelines USDA Sampling Procedures for PDP 6.1.2–3 WHO Technical Report Series, #986, Annex 2, 10 The system shall allow training sessions to be scheduled for personnel. 29 CFR Part 1910.1450 (f) ABFT Accreditation Manual Sec. B ASCLD/LAB Supp. Reqs. for the Accreditation of Forensic Science Testing Laboratories 5.2.7 ASTM E1578-18 E-1-2 FDA Hazard Analysis Critical Control Point Guidelines The system should provide access to relevant training materials to personnel attending training sessions.