ML19154A546
| ML19154A546 | |
| Person / Time | |
|---|---|
| Issue date: | 06/03/2019 |
| From: | Annette Vietti-Cook NRC/SECY |
| To: | |
| Shared Package | |
| ML19154A539 | List: |
| References | |
| Download: ML19154A546 (116) | |
Text
FEDERAL REGISTER*****
Federal Register Code of Federal Regulations Federal Register***
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Federal RegisterFederal Register
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Definitions cancelled testcarryoverCertifying ScientistFederal custody and control formlotrejected for testing,Responsible Personcalibratorcontroldilute specimenHHS-certified laboratoryinvalid resultlimit of quantitationsubstituted specimenCancelled testcancelled test cancelled testcancelled testcancelled testcancelled test Carryovercarryover CarryoverCarryovercarryovercarryovercarryovercarryover carryoverCertifying ScientistCertifying ScientistCertifying ScientistFederal custody and control form (Federal CCF)Federal custody and control form (Federal CCF) Federal RegisterFederal CCF Federal CCF, Federal CCFFederal CCF Lotlotlot lotRejected for testingrejected for testingrejected for testing Responsible PersonResponsible PersonResponsible PersonCalibratorcalibratorcalibratorControlcontrolcontrol Dilute specimendilute specimenHHS-certified laboratoryHHS-certified laboratoryFederal RegisterHHS-certified laboratoryHHS-certified laboratory HHS-certified laboratoryFederal RegisterInvalid resultinvalid resultinvalid result Limit of QuantitationLimit of Quantitation (LOQ)
Substituted specimensubstituted specimenDrug Testing Panel Additions Federal Register Revised Initial Drug Testing Cutoff Levels Revised Confirmatory Drug Testing Cutoff Levels
Validity Testing of Adulterants at HHS-Certified Laboratories Special Analyses Testing of Urine Specimens
Alternative Specimen Collection Sites Federal Register Federal RegisterFederal Register Specimen Collection Procedures
adulterated specimen Collector Actions Following a Refusal to Test
Blind Performance Test Sample Lot In-Service Requirement HHS-Certified Laboratory PersonnelQualifications and Responsibilities HHS-Certified Laboratory Procedures
Quality Control Samples for Validity and Drug Testing
Federal Register Additional MRO Review for Invalid Specimens with pH of 9.0 to 9.5
Donor Request for Specimen Retesting or Bottle B Testing
Collection of a Second Specimen under Direct Observation when Bottle B or an Aliquot of a Single Specimen Is Not Available for Testing FFD Program Performance Data Reporting
Nomenclature Changes § 26.4 FFD program applicability to categories of individuals
§ 26.5 DefinitionsCcancelled test, CcarryoverCertifying ScientistFederal custody and control formLl otRrejected for testingResponsible Person calibrator control dilute specimen HHS-certified laboratoryFederal RegisterHHS-certified laboratory Mandatory Guidelines for Federal Workplace Drug Testing Programs invalid result limit of quantitation (LOQ)substituted specimen
§ 26.8 Information collection requirements: OMB approval
§ 26.31 Drug and Alcohol Testing§ 26.89 Preparing to Collect Specimens for Testing
§ 26.107 Collecting a Urine Specimen
§ 26.109 Urine Specimen Quantity§ 26.111 Checking the Acceptability of the Urine Specimen
§ 26.115 Collecting a Urine Specimen under Direct Observation
§ 26.117 Preparing Urine Specimens for Storage and Shipment § 26.129 Assuring Specimen Security, Chain of Custody, and Preservation
§ 26.133 Cutoff Levels for Drugs and Drug Metabolites
§ 26.137 Quality Assurance and Quality Control
§ 26.153 Using Certified Laboratories for Testing Urine Specimens Federal Register
§ 26.155 Laboratory Personnel § 26.157 Procedures § 26.159 Assuring Specimen Security, Chain of Custody, and Preservation
§ 26.161 Cutoff Levels for Validity Testing
§ 26.163 Cutoff Levels for Drug and Drug Metabolites
§ 26.165 Testing Split Specimens and Retesting Single Specimens
§ 26.167 Quality Assurance and Quality Control
§ 26.168 Blind Performance Testing
§ 26.169 Reporting Results § 26.183 Medical Review Officer § 26.185 Determining a Fitness-for-Duty Policy Violation
§ 26.405 Drug and Alcohol Testing§ 26.415 Audits
§ 26.717 Fitness-for-duty program performance data
Alignment with the HHS Guidelines Special Analyses TestingProvide Flexibility to Conduct Additional Specimen Validity Tests Effective Date of the Final RuleFederal RegisterFederal Register Direct Observation of Specimen Collection 2017 HHS Guidelines - New Test Analyes Methylenedioxyethylamphetamine i.e.
FEDERAL REGISTER Draft Regulatory Guidance
Type of submission, new or revision:
The title of the information collection:The form number if applicable:How often the collection is required:
Who will be required or asked to report:An estimate of the number of annual responses:
The estimated number of annual respondents: An estimate of the total number of hours needed annually to complete the requirement or request
FEDERAL REGISTERPublic Protection Notification Federal Register Code of Federal Regulations
FEDERAL REGISTER
FEDERAL REGISTER
FEDERAL REGISTER
cancelled testcarryoverCertifying ScientistFederal custody and control formlotrejected for testingResponsible Person calibratorcontroldilute specimenHHS-certified laboratoryinvalid resultlimit of quantitation substituted specimenCalibratorCancelled test cancelled test CarryoverCertifying Scientist ControlDilute specimen Federal custody and control form (Federal CCF) Federal Register HHS-certified laboratoryMandatory Guidelines for Federal Workplace Drug Testing ProgramsInvalid result Limit of quantitation (LOQ)Lot Rejected for testingResponsible PersonSubstituted specimen Substances tested
Initial drug testing.
Confirmatory drug testing
Responsibilities