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DrugCheck ® Onsite DRUG TESTING TRAINING

DrugCheck Onsite DRUG TESTING TRAINING - · PDF fileDRUG TESTING TRAINING. A. Drugs of Abuse and Testing Overview 1. Trends in Drug Use 2. Who’s using drug testing? 3. Types of Testing:

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DrugCheck® Onsite

DRUG TESTING TRAINING

A. Drugs of Abuse and Testing Overview

Trends in Drug Use1. Who’s using drug testing?2. Types of Testing: Screening, Confi rmation3. Detection Times and Cutoff Levels4. False Positives5. Adulteration of Samples6. Interpretation of Results7. Drug Screenings Offered by DrugCheck8. ®

B. DrugCheck® NxScan Cup Features/benefi ts1. Cup operation2.

C. DrugCheck® NxStep CupFeatures/benefi ts1. Cup operation2.

D. DrugCheck® Dip TestFeatures/benefi ts1. Dip operation2.

E. DrugCheck® Training Exam

CONTENTS

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DRUGCHECK® NXSCAN CUP

Features and Benefi ts

✓ Results in 5 minutes

✓ Photocopy or scan results for permanent record (template included)

✓ Cup lies fl at on copier or scanner for clear copying

✓ Simultaneous detection of up to 14 drugs, adulterants and/or alcohol

✓ Easy interpretation and better sensitivity

✓ Unbreakable cup surface

✓ Lab accuracy

✓ Tamper-proof strip insert

✓ Patented technology

✓ FDA cleared

✓ Made in the U.S.A.

Temperature strip

✓ NO ASSEMBLY ✓ NO MOVING PARTS

✓ NO TILTING OR TIPPING TO ACTIVATE

✓ NO CROSS CONTAMINATION

Let OMSdo the work!Web-based results

management

Available with alcohol and/or adulterants (Specifi c Gravity, pH, Oxidants)

DRUGCHECK® NXSCAN CUP

Procedure: Specimen Collection

Have available for use a Chain of 1. Custody form (COC) or Test Results Record template.

Require the donor to present a 2. photo identifi cation.

Ask donor to remove any 3. unnecessary outer clothing and empty all pockets.

Keep all backpacks and purses 4. out of the restroom. Insure that all backpacks, wallets and purses are secured, preferably in a locked cabinet. If using a lockable cabinet or container, make sure that the donor is given the key.

Secure the collection site (restroom).5.

Turn off water sources (sink faucets), ensure blue toilet water, inspect site

for and remove cleaners and other substances, secure toilet tank top or blue tank water.

Visually inspect foil package 6. containing the cup to ensure that the package has not been compromised. Tear open the foil pouch and remove the test cup.

Issue the device to the individual to 7. be tested. Instruct the donor not to fl ush the toilet or turn the water on and to open the door when they are done.

Have the individual urinate directly 8. into the DRUGCHECK

® Test Cup. Ensure that the specimen is above the minimum level (30 mL) line on the test label.

NOTE: Urine specimens can be transferred from a urine collection container into the DRUGCHECK

® Test Cup, if necessary.

DRUGCHECK® NXSCAN CUP

Procedure: Specimen Collection 9. Check temperature (normal range from 90° to 100°F or 32° to 38°C) and observe specimen for foreign material and/or discoloration.

If the temperature is not within the normal range, the specimen is considered invalid and must be retested.

10. Pull privacy label and read drug test strip results at 5 minutes. Read adulterant strips at 1 minute and alcohol strips at 2 minutes.

11. Secure container by tightening lid as far as it will turn, apply security seal, and have donor and test administrator both sign and date seal, as well as initial and date the NxScan label.

Peel the privacy label. Read results at 5 minutes.

DRUGCHECK® NXSCAN CUP

Procedure: Scanning or Copying Results

Firmly tighten cup lid to avoid leakage. Copy or scan results

for permanent record.

NOTE: If confi rmation is required, secure specimen in appropriate shipping container and send to a confi rmation lab with signed Chain of Custody form.

12. Ensure that lid is fi rmly tightened. With Test Results Record template on copier or scanner, place NxScan cup face down in the Results Window opening of the template (optional).

13. Copy or scan results using Test Results Record template (optional). Cups containing test strips on front and back will require turning over the template and cup to copy/scan opposite sides.

14. Fill out Test Results Record with complete donor and test information.

12. Ensure that lid is fi rmly tightened. With Test Results Record template on copier or scanner, place NxScan cup face down in the Results Window opening of the template (optional).

13. Copy or scan results using Test Results Record template (optional). Cups containing test strips on front and back will require turning over the template and cup to copy/scan opposite sides.

14. Fill out Test Results Record with complete donor and test information.

Company Name _______________________________________________________________ Phone _________________ Fax _________________

Address ____________________________________ City ____________________________ State/Province __________ Zip/Postal Code __________

Employee I.D. _____________________________________________

Last Name _____________________________________________________ First Name _______________________________________________

Type of Identification Provided: q Driver’s License q Employee Photo I.D. q Other ________________________________________________

Reason for test: q Pre-employment q Random q Reasonable cause q Post-accident q Other _____________________________________

Date/Time Collected __________________________________ Time Interpreted ________________________

Specimen Temperature: q Normal: 90° to 100°F (32° to 38°C) q Other _____

Drug Name Symbol Negative Positive Not Tested

Cocaine COC q q q

Marijuana THC q q q

Opiates OPI q q q

Amphetamine AMP q q q

Phencyclidine PCP q q q

Benzodiazepine BZO q q q

Barbiturate BAR q q q

Methadone MTD q q q

Methamphetamine MET q q q

Tricyclic Antidepressants TCA q q q

Ecstasy MDMA q q q

Propoxyphene PPX q q q

Oxycodone OXY q q q

Bupenorphrine BUP q q q

__________________ ______ q q q

Adulterants Normal Abnormal Not Tested

1. Creatinine (CR) q q q

2. Nitrite (NI) q q q

3. pH (pH) q q q

4. Specific gravity (SG) q q q

5. Oxidants (OX) q q q

Nicotine Negative Positive Not Tested

1. Cotinine (COT) q q q

I hereby certify that the specimen provided is my own and has not been substituted or adulterated. I further agree and grant

permission for the testing of my specimen for drug metabolites and alcohol.

________________________________________________________ ____________________________

Donor signature Date / Time

I hereby certify that I collected the specimen provided by the aforementioned Donor and that it was not substituted or

adulterated to the best of my knowledge. The specimen temperature and color were acceptable.

________________________________________________________ ____________________________

Collector signature Date / Time

________________________________________________________ ____________________________

Laboratory signature Date / Time received

Alcohol 0% 0.04 0.08 0.20

1. Alcohol q q q q

Results Window 1 (Side 1 test strips)1. Firmly tighten cup lid to avoid leakage.

2. Place SIDE 1 (this side) of Test Results

Record face down on copier or scanner.

3. With cup lid secure, place Side 1 of the

cup face down in the opening below.

4. Copy or scan.

NOTE: If your cup includes additional test strips on the

opposite side of the cup (Side 2),

turn over this template and place

SIDE 2 face down on copier or

scanner to copy the results of the additional test strips.

IMPORTANT: Firmly tighten cup lid to avoid leakage. Place this

side of the page, and window of Side 1 of cup, face down on copier

or scanner to copy results.

Remove this perforated panel

for Results Window opening

SIDE 1TEST RESULTS RECORD

Test Reference Number ________________________ Name of Collector ______________________________________________________

Note: Temperature must be read within four

minutes of collection. Positive results must be

confirmed by laboratory.

TesT ResulTs

CeRTiFiCaTion

DonoR inFoRmaTion

Company inFoRmaTion

Notes / Comments _________________________________________________________________________________________________________

_______________________________________________________________________________________________________________________

_______________________________________________________________________________________________________________________

DRUGCHECK® NXSCAN CUP

Procedure: Interpretation of Results

DC107C 0608

Adulteration Color Comparison ChartAbnormal

(Low)Test Strip

TestReading Time

2 3 4 5 7 9 ≥10

pHImmediate

1.000 1.005 1.015 1.025 ≥1.030

SpecificGravity (SG)

45 seconds

PositiveNegative

Oxidants(OX)

30 seconds

Abnormal(High)Normal

(example of strip as it may appear in cup)

ADULTERANT strips test for oxidants, specifi c gravity and pH. Specimens that have not been adulterated will display normal color range on the pad. Abnormal results (high or low) require collection of a new specimen and re-testing. Read adulterant results at 1 minute.

NOTE: Results must be read at1 minute as pad color may change.

DRUGCHECK® NXSCAN CUP

Procedure: Interpretation of Results

Alcohol Color Chart 0% 0.04% 0.08% 0.20%

DC121 0507

ALCOHOL strips test for the presence of alcohol at specifi c thresholds. Use the Alcohol Color Chart to compare with the color pad on the test strip. Read alcohol results at 2 minutes.

NOTE: Results must be read at2 minutes as pad color may change.

Example: 0.20% alcohol

DRUGCHECK® NXSCAN CUP

Procedure: Interpretation of Results

NEGATIVE Two lines appear. One line visible in the control region (C), and another apparent line adjacent visible in the test region (T). This negative result indicates that the drug concentration is below the detectable level.

NOTE: The shade of color in the test line region (T) will vary, but it should be considered negative if a line is visible. There is no meaning attributed to the line color intensity or width.

POSITIVE One line appears in the control region (C). No line whatsoever appears in the test region (T). The lack of a line in the test region (T) indicates a preliminary positive result for the corresponding drug of that specifi c test region. Send this urine specimen to a certifi ed laboratory for a more specifi c confi rmation by GC/MS.

INVALID Control line fails to appear. Insuffi cient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test using a new test device. If the problem persists, contact your supplier for technical support.

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DrugCheck® Onsite

DRUG TESTING TRAINING

For more information, contact your distributor.