WHAT WE DO - THE COLLECTION & TESTING PROCESS

We ensure our restricted collection facility is clean and inspected before and after every collection.

We obtain valid picture identification of every Donor, to ensure we test the right person.

We don't perform any services, without first obtaining the Donor's written consent (DOT exempt).

We select the correct CCF for the type of collection ordered.  We ensure each step is followed in sequential order.

We allow the Donor to select their own sample collection cup, to help strengthen the integrity of the collection process.

We visually check for suspected adulterants & substitution devices, including donor's wallet.  Donor then washes hands.

If the Donor presents no suspect items, the Donor is permitted to provide their sample in complete privacy, behind a full length door.

While the Donor provides their sample within the enclosed restroom, our Certified Collectors listen for sounds of tampering.

We conduct a full inspection of the sample provided to ensure proper volume, temperature, coloration and consistency are within range.

Acceptable samples are split into two separate vials, sealed with barcoded tamper evident tape, in the Donor's presence.

Donor initials the barcoded seals to verify the sample ID from each bottle, matches the CCF.  The samples & the CCF are packaged.

Completed collections are kept in secured storage, until picked up by a licensed express carrier, enroute to our DHHS/SAMHSA certified lab.

All samples accessioned at our labs are checked and scanned to ensure the CCF & Barcodes match.

Accessioners check for proper volume, color, consistency, leakage and collector/shipping errors.

All samples are screened for adulterants and the creatine & specific gravity are confirmed.

All samples are then issued an internal accessioning number and placed into the EMIT screening sequence for initial testing.

All Non-Negative EMIT samples are automatically re-tested via LC/MS/MS to specifically ID the drug found & quantify it.

Once the lab EMIT screens and LC/MS/MS confirms the Donor's sample, the results are forwarded to the MRO for review w/Donor.

The Medical Review Officer process is the Donor's one and only chance to speak with a Medical Doctor about the lab's findings.

If the M.R.O. is unable to verify the Donor's alternative medical explanation(s), it is reported as a "Verified Positive".

Once the Lab & the MRO have completed their process, all findings are sent to FDTSI for one final Q.C. check and verification.