search.noResults

search.searching

dataCollection.invalidEmail
note.createNoteMessage

search.noResults

search.searching

orderForm.title

orderForm.productCode
orderForm.description
orderForm.quantity
orderForm.itemPrice
orderForm.price
orderForm.totalPrice
orderForm.deliveryDetails.billingAddress
orderForm.deliveryDetails.deliveryAddress
orderForm.noItems
Why after 30 years did an agency not known for change or flexibility (no offense intended), suddenly turn an entire industry on its head?


Figure 1: Oral fluid provides a shorter window of detection than other testing methods combined with non-invasive collections.


However, these new guidelines are not a direct response to what’s happening with marijuana laws across the country, but they do align well with the controversial trend toward full legalization. So, if these new regulations are not


the federal government’s response to legalization, then why did SAMHSA spend years on this project? Why aſter 30 years did an agency not known for change or flexibility (no offense intended), suddenly turn an entire industry on its head? Tere were actually many good reasons, but three seem to stand out the most: combating adulteration, cuting the time and costs of a typical drug test, and the science of the technology behind lab- based oral fluid testing. Regarding drug test cheating, SAMHSA states:


All unobserved specimen collections are at risk for substitution and adulteration. Studies conducted by the drug testing industry indicate that 0.05 to 3% of urine specimens collected for drug use detection are determined to be substituted or adulterated. Oral fluid collections will occur under observation, which should substantially lessen the risks of specimen substitution and adulteration that has been associated with urine specimen collections, most of which are unobserved.


10 datia focus


On the subject of cuting time and costs, SAMHSA offered the following:


Oral fluid collection can require less time than urine collection, reducing employee time away from the workplace and, therefore, reducing costs to the … employer.


In the OFMG, SAMHSA also


emphasized that oral fluid collections do not require a facility that provides visual privacy during the collection and that the agency anticipates that “many oral fluid collections will occur at or near the workplace, and not at a dedicated collection site, thereby reducing the amount of time away from the workplace.” Employers will have the option to collect


a urine specimen when a donor is unable to provide an oral fluid specimen (and vice versa), which will “reduce both the need to reschedule a collection and the need for the MRO to arrange a medical evaluation of a donor’s inability to provide a specimen.” Perhaps, the greatest time and cost


savings cited by SAMHSA was the reduction in the overall time needed to administer an oral fluid test.


Administrative data for urine collections indicates it takes, on average, about 4 hours from the start of the notification of the drug test to the actual time a donor reports back


2020 • Issue 2


Page 1  |  Page 2  |  Page 3  |  Page 4  |  Page 5  |  Page 6  |  Page 7  |  Page 8  |  Page 9  |  Page 10  |  Page 11  |  Page 12  |  Page 13  |  Page 14  |  Page 15  |  Page 16  |  Page 17  |  Page 18  |  Page 19  |  Page 20  |  Page 21  |  Page 22  |  Page 23  |  Page 24  |  Page 25  |  Page 26  |  Page 27  |  Page 28  |  Page 29  |  Page 30  |  Page 31  |  Page 32  |  Page 33  |  Page 34  |  Page 35  |  Page 36  |  Page 37  |  Page 38  |  Page 39  |  Page 40  |  Page 41  |  Page 42  |  Page 43  |  Page 44  |  Page 45  |  Page 46  |  Page 47  |  Page 48