10.3 How is a blind sample submitted to an HHS-certified laboratory?.10.1 What are the requirements for federal agencies to submit blind samples to HHS-certified laboratories or IITFs?.Subpart J-Blind Samples Submitted by an Agency.9.5 What are the qualitative and quantitative specifications of performance testing (PT) samples?.Subpart I-HHS Certification of Laboratories and IITFs.8.12 How is a monitored collection conducted?.8.10 How is a direct observed collection conducted?.8.9 When is a direct observed collection conducted?.8.8 How does the collector prepare the urine specimens?.8.7 If the donor is unable to provide a urine specimen, may another specimen type be collected for testing?.
8.6 What procedure is used when the donor states that they are unable to provide a urine specimen?. 8.5 What steps does the collector take during and after the urine specimen collection procedure?. 8.4 What steps does the collector take in the collection procedure before the donor provides a urine specimen?. 8.3 What are the preliminary steps in the urine specimen collection procedure?. 8.1 What privacy must the donor be given when providing a urine specimen?. Subpart H-Urine Specimen Collection Procedure. 6.2 What happens if the correct OMB approved Federal CCF is not available or is not used?. 6.1 What federal form is used to document custody and control?. Subpart F-Federal Drug Testing Custody and Control Form (CCF). 4.4 What are the requirements to be an observer for a direct observed collection?. 3.9 What criteria are used to report an invalid result for a urine specimen?. 3.8 What criteria are used to report a urine specimen as dilute?. 3.6 What criteria are used to report a urine specimen as adulterated?. 3.5 May an HHS-certified laboratory perform additional drug and/or specimen validity tests on a specimen at the request of the Medical Review Officer (MRO)?. 3.4 What are the drug test cutoff concentrations for urine?. 3.3 May any of the specimens be used for other purposes?. 3.2 May a specimen be tested for additional drugs?. 3.1 Which tests are conducted on a urine specimen?. 2.2 Under what circumstances may a urine specimen be collected?. 2.1 What type of specimen may be collected?. 1.8 What are the potential consequences for refusing to take a federally regulated drug test?. 1.7 What is a refusal to take a federally regulated drug test?. 1.6 What is an agency required to do to protect employee records?. 1.5 What do the terms used in these Guidelines mean?. Medical Review Officer (MRO) Requalification-Continuing Education Units (CEUs). Proposed New Analytes: Oxycodone, Oxymorphone, Hydrocodone, and Hydromorphone. Summary of Public Comments and HHS's Response. This repetition of headings to form internal navigation links Headings within the legal text of Federal Register documents. This table of contents is a navigational tool, processed from the Provide legal notice to the public or judicial notice to the courts. Rendition of the daily Federal Register on does not Until the ACFR grants it official status, the XML Legal research should verify their results against an official edition of #FEDERAL REGISTER 2017 TDIU CHANGES PDF#
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