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In the realm of employment and regulatory compliance, the Federal Drug Testing Custody and Control Form stands as a crucial document. This extensive form encompasses various pivotal elements ranging from the initial collection of specimen details by the collector or an employer representative to the final steps of reporting and certification by testing laboratories. Notably, the form details the types of drug tests to be administered, including substances like THC, COC, PCP, OPI, and AMP, among others, underlining its comprehensive approach to drug screening. Furthermore, it specifies different reasons for testing, such as pre-employment, random, post-accident, and reasonable suspicion, catering to a wide array of workplace and regulatory scenarios. The involvement of multiple parties, from the employer and the donor to collectors and laboratory personnel, each playing a distinct role in ensuring the integrity and accuracy of the testing process, is meticulously documented through the form. Quest Diagnostics, as mentioned, is one of the recognized entities associated with these procedures, indicating the form's engagement with established testing laboratories. This detailed form not only ensures adherence to federal requirements but also facilitates a transparent, accountable, and standardized process for drug screening, reflecting its pivotal role in workplace safety and compliance.

Form Preview Example

FEDERAL DRUG TESTING CUSTODY AND CONTROL FORM

800-877-7484

SPECIMEN ID NO.

 

STEP 1: COMPLETED BY COLLECTOR OR EMPLOYER REPRESENTATIVE

LAB ACCESSION NO.

Quest, Quest Diagnostics, the associated logo and all associated Quest Diagnostics marks are the trademarks of Quest Diagnostics Incorporated. © Quest Diagnostics Incorporated. All rights reserved. QD20315-FED. Revised 10/10. SC2K - 111192.

A. Employer Name, Address, I.D. No.

 

 

B. MRO Name, Address, Phone and Fax No.

 

 

 

 

 

 

 

 

 

C. Donor SSN or Employee I.D. No. _______________________________________________________________

 

 

 

 

D. SpecifyTesting Authority: HHS

NRC

DOT – Specify DOT Agency: FMCSA

FAA

FRA FTA PHMSA USCG

E. Reason forTest: Pre-employment

Random

Reasonable Suspicion Cause Post Accident

Return to Duty

Follow-up Other (specify) ____________________________

F. DrugTests to be Performed:

THC, COC, PCP, OPI, AMP

THC & COC Only

Other (specify) ________________________________________________

G. Collection Site Name:

 

 

 

 

 

Collection Site Code:

 

 

 

 

Address:

 

 

 

 

 

 

Collector Phone No.:

 

 

City, State and Zip:

 

 

 

 

 

Collector Fax No.:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

STEP 2: COMPLETED BY COLLECTOR (make remarks when appropriate) Collector reads specimen temperature within 4 minutes.

Temperature between 90° and 100° F? Yes No, Enter Remark

Collection: Split Single None Provided, Enter Remark

Observed, (Enter Remark)

REMARKS

STEP 3: Collector affixes bottle seal(s) to bottle(s). Collector dates seal(s). Donor initials seal(s). Donor completes STEP 5 on Copy 2 (MRO Copy)

STEP 4: CHAIN OF CUSTODY - INITIATED BY COLLECTOR AND COMPLETED BY TEST FACILITY

 

I certify that the specimen given to me by the donor identified in the certification section on Copy 2 of this form was

 

SPECIMEN BOTTLE(S) RELEASED TO:

 

collected, labeled, sealed, and released to the Delivery Service noted in accordance with applicable Federal requirements.

Quest Diagnostics Courier

 

 

X

 

 

 

 

 

FedEx

 

 

Signature of Collector

 

 

 

 

 

Other

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

AM

 

 

 

 

 

 

 

 

 

PM

 

 

 

 

 

(Print) Collector's Name (First, MI, Last)

Date (Mo./Day/Yr.)

 

Time of Collection

 

 

Name of Delivery Service

RECEIVED AT LAB OR IITF:

 

 

 

 

 

Primary Specimen

SPECIMEN BOTTLE(S) RELEASED TO:

 

X

 

 

 

 

 

Bottle Seal Intact

 

 

 

 

 

 

 

Yes No

 

 

 

Signature of Accessioner

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

If No, Enter remarks

 

 

 

 

 

 

 

 

 

in Step 5A.

 

 

 

(Print) Accessioner’s Name (First, MI, Last)

 

 

 

Date (Mo./Day/Yr.)

 

STEP 5A: PRIMARY SPECIMEN REPORT - COMPLETED BY TEST FACILITY

NEGATIVE

POSITIVE for:

Marijuana Metabolite ( 9-THCA)

6- Acetylmorphine

Methamphetamine

MDMA

DILUTE

 

 

Cocaine Metabolite (BZE)

Morphine

Amphetamine

MDA

 

 

 

PCP

Codeine

 

MDEA

REJECTED FOR TESTING

ADULTERATED

SUBSTITUTED

INVALID RESULT

 

 

REMARKS:

Test Facility (if different from above):

I certify that the specimen identified on this form was examined upon receipt, handled using chain of custody procedures, analyzed, and reported in accordance with applicable Federal requirements.

X

Signature of Certifying Scientist

(Print) Certifying Scientist's Name (First, MI, Last)

Date (Mo./Day/Yr.)

STEP 5b: COMPLETED BY SPLIT TESTING LABORATORY

RECONFIRMED FAILED TO RECONFIRM - REASON ____________________________________________

___________________________________________

I certify that the split specimen identified on this form was examined upon receipt, handled using chain of custody

procedures, analyzed and reported in accordance with applicable Federal requirements.

 

 

 

 

 

 

 

 

 

 

 

 

Laboratory Name

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

___________________________________________

X

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Signature of Certifying Scientist

 

 

 

(Print) Certifying Scientist's Name (First, MI, Last)

Date (Mo./Day/Yr.)

 

 

 

 

 

 

 

Laboratory Address

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

OMB No. 0930-0158

PRESS HARD - YOU ARE MAKING MULTIPLE COPIES

File Characteristics

Fact Detail
Form Title FEDERAL DRUG TESTING CUSTODY AND CONTROL FORM
Contact Number 800-877-7484
Form Number QD20315-FED
Last Revision Date Revised 10/10
Associated Company Quest Diagnostics Incorporated
Specimen ID Number Location Provided at the top of the form
Governing Testing Authorities HHS, NRC, DOT (specific DOT agencies include FMCSA, FAA, FRA, FTA, PHMSA, USCG)

Steps to Writing Drug Screen

Filling out the Federal Drug Testing Custody and Control Form is a crucial step in ensuring the integrity and legality of the drug screening process. This process involves several parties, including the collector or employer representative, the donor, and laboratory personnel, each with specific roles and responsibilities. By understanding and accurately completing each required section, the involved parties can uphold the validity of the drug test results. Below is a step-by-step guide to help you thoroughly fill out the form without missing any critical information.

  1. Step 1: Completed by Collector or Employer Representative
    • Enter the Employer Name, Address, and I.D. No. in the designated area.
    • Fill in the MRO (Medical Review Officer) Name, Address, Phone and Fax No.
    • Provide the Donor SSN or Employee I.D. No. to accurately identify the individual taking the test.
    • Specify the Testing Authority (e.g., HHS, NRC, DOT) and, if DOT, specify the DOT Agency (e.g., FMCSA, FAA).
    • Indicate the Reason for Test (e.g., Pre-employment, Random, Reasonable Suspicion/Cause).
    • Select the Drug Tests to be Performed, choosing from options like THC, COC, PCP, OPI, AMP, or other specified tests.
    • Fill in the Collection Site Name, Code, Address, Collector Phone No., and other site information.
  2. Step 2: Completed by Collector
    • Record the specimen temperature within 4 minutes of collection, ensuring it's between 90° and 100° F. If not, enter a remark.
    • Mark the type of collection (Split or Single) and note any observations or issues.
    • Include any additional remarks if necessary.
  3. Step 3: Collector affixes bottle seal(s)
    • The collector then affixes the seal(s) to the bottle(s), dates the seal(s), and has the donor initial them.
  4. Step 4: Chain of Custody
    • The collector initiates the chain of custody, which is completed by the test facility. This includes certifying that the specimen was collected, labeled, sealed, and released correctly.
    • Fill in the collector's name, the date, and time of collection, and specify the name of the delivery service used.
  5. Step 5a & 5b: Completed by Test Facility and Split Testing Laboratory (if applicable)
    • These steps are for laboratory personnel to complete based on the analysis of the primary and, if applicable, the split specimen.
    • Include results, any remarks, and certification by the certifying scientist(s).

By carefully following these steps, each party can ensure that the drug screening process is executed properly and that the results are accurate and reliable. Remember, accuracy and attention to detail are paramount when filling out any legal document to prevent potential legal issues and ensure the drug screening process adheres to federal guidelines.

Important Details about Drug Screen

What is the purpose of the Federal Drug Testing Custody and Control Form?

This form is used to document and ensure the integrity of the process when a drug screen is conducted. It tracks the specimen from the time it is collected until the analysis is completed. This includes documentation by the collector, the delivery to the testing facility, analysis by the testing facility, and the reporting of the results. This process ensures that the specimen is properly handled and unaltered throughout the testing procedure.

How is the specimen collected and what types of drug tests are performed?

Specimens are collected by a trained collector who ensures that the collection process meets federal requirements, including the correct temperature range (90° to 100° F) within 4 minutes of collection. The types of drug tests to be performed can include, but are not limited to, substances like THC (marijuana metabolite), COC (cocaine metabolite), PCP, OPI (opioids), AMP (amphetamines), and others as specified by the employer or the testing authority.

What does the "Reason for Test" section cover?

The "Reason for Test" section indicates the specific reason why the drug screen is being conducted. Options include pre-employment screening, random testing, reasonable suspicion/cause, post-accident testing, return to duty, follow-up, among other specified reasons. This helps clarify the context of the test for all parties involved.

What happens if the specimen temperature is not within the required range?

If the specimen's temperature is not within the required range of 90° to 100° F within 4 minutes of collection, the collector must enter a remark on the form. This may indicate potential issues with the sample's validity, leading to further investigation or a request for another specimen to be collected and tested.

Can you explain the chain of custody process documented on this form?

The chain of custody process is initiated by the collector, who ensures that after the specimen is collected, it is correctly labeled, sealed, and then released to the delivery service noted on the form (e.g., Quest Diagnostics Courier, FedEx). This process is meticulously documented to confirm that the specimen handed over to the testing facility is the same as what was collected and that it has been securely transported and received without tampering.

What does it mean if a specimen is marked as "REJECTED FOR TESTING," "ADULTERATED," or "SUBSTITUTED"?

If a specimen is marked as "REJECTED FOR TESTING," it indicates that there was an issue that prevented it from being tested, such as improper labeling or damage during transport. "ADULTERATED" refers to a specimen that appears to have been tampered with, in an attempt to manipulate the test results. A "SUBSTITUTED" result suggests the specimen does not have characteristics of human urine, indicating potential cheating in the test process. In all these cases, further action will be required, potentially including the collection and testing of a new specimen.

Common mistakes

When filling out the Federal Drug Testing Custody and Control Form, it's crucial to avoid common mistakes to ensure the process goes smoothly. One significant mistake is not accurately filling in the Employer Name, Address, I.D. No. This information is essential for identifying the employer and must match the records exactly. An incorrect or incomplete employer identification can lead to delays or misinterpretation of results.

Another common error occurs in the section requiring the MRO (Medical Review Officer) Name, Address, Phone, and Fax No. The integrity of the entire testing process can be compromised if this information is incorrect or missing, as the MRO is responsible for reviewing and interpreting the test results. It's critical to ensure that this information is current and accurate.

The form requires the Donor's SSN or Employee I.D. No. Mistakes in this section can lead to serious privacy breaches or result in the results being sent to the wrong person or entity. It is imperative to double-check this information for accuracy.

Selecting the correct Testing Authority and Specific DOT Agency, when applicable, is another area where mistakes are commonly made. This selection directly impacts the regulatory standards applied to the test, and failure to select the correct option can result in non-compliance with federal regulations.

Errors in indicating the Reason for the Test can have significant repercussions. For example, marking "Pre-employment" instead of "Reasonable Suspicion Cause" or "Post Accident" can affect the procedural follow-ups and how the results are interpreted and acted upon.

When listing the Drugs to be Tested for, specificity is essential. Assuming all panel tests are the same or omitting specific substances because of assumptions or oversight can result in incomplete testing that doesn't meet the employer's or regulatory requirements.

The Collection Site Information is often overlooked. Incorrect or incomplete information in this section can lead to confusion or challenges in verifying the test's location, potentially questioning the specimen's chain of custody.

A critical step that is often mishandled is ensuring the specimen bottle's seal is initialed by the donor. This oversight can lead to questions regarding the specimen's integrity and may necessitate a re-collection, causing delays and increased costs.

Finally, failure to press hard enough to ensure all copies of the form are legible is a surprisingly common mistake. This form serves as a legal document, and unclear or incomplete copies can be problematic if the results are contested or audited. Ensuring that all information is transferred to each copy of the form is essential for the validity of the process.

Documents used along the form

When managing the drug screening process, it's essential to have a complete set of documents to ensure that the procedure is carried out effectively and complies with relevant regulations. Alongside the Federal Drug Testing Custody and Control Form, several other forms and documents play crucial roles in this multifaceted process. Here is a brief overview of four such documents often used in conjunction with the drug screen form.

  1. Consent and Release Form: This document is obtained from the individual undergoing the drug test. It ensures they are aware of the testing procedure and provides their consent for the drug test and the release of the results to the authorized parties.
  2. Medical Review Officer (MRO) Report Form: Completed by a medical review officer, this form is used to review and interpret the results of the drug test. It serves as a final verification step, determining if there is a medical explanation for any substances detected during the screening.
  3. Substance Abuse Professional (SAP) Assessment Report: If a test result is positive, this report outlines the evaluation and recommendations made by a Substance Abuse Professional, detailing any necessary treatment or follow-up testing for the employee.
  4. Return-to-Duty Agreement: For employees who have violated a drug and alcohol program policy and are returning to work, this document outlines the terms and conditions of their return. It may include follow-up tests, treatment programs, and ongoing evaluations to ensure compliance.

Each document serves its purpose in maintaining the integrity and efficiency of the drug testing process. The completion and proper management of these documents ensure that both employers and employees meet the required legal and procedural standards. This collaborative documentation effort contributes to a safer and more compliant workplace environment.

Similar forms

The Employment Verification Form shares similarities with the Federal Drug Testing Custody and Control Form, primarily in its purpose to collect and verify personal information. Similar to how the drug screen form requires details such as employer name, employee ID, and the type of tests to be performed, the Employment Verification Form collects data regarding an employee’s position, duration of employment, and salary information. Both forms serve as official documents that confirm specific attributes or actions of individuals within a professional context, ensuring those attributes or actions are accurately recorded for legal or procedural purposes.

Medical Consent Forms are also akin to the drug screening form in several ways, especially regarding the collection and documentation of consent regarding medical procedures or tests. Like the drug screen form, which includes details about the type of drug tests to be performed and requires the donor's verification, a Medical Consent Form must have detailed information about the medical procedure in question and obtain explicit consent from the patient or their guardian. Both forms are essential for maintaining a record of informed consent and adherence to privacy regulations and ethical standards in handling sensitive information.

The Background Check Authorization Form parallels the drug screen form in its function of gathering personal details necessary for conducting checks or tests with the aim of evaluating suitability. This form typically collects information such as social security number, previous addresses, and consent to perform background checks, mirroring the drug screen form’s collection of the donor's SSN and consent for drug testing. Both forms are pivotal in the decision-making processes for employment or other forms of eligibility, requiring explicit consent to proceed with the verification or testing process.

Chain of Custody Forms share a direct resemblance to the particular section of the drug screen form dedicated to tracking the specimen’s movement and handling. They meticulously document each individual or entity that receives, handles, or transfers the specimen, ensuring that the integrity and security of the sample are maintained throughout the testing process. This procedural documentation is critical in both contexts for establishing the reliability of the test results by safeguarding against tampering, contamination, or misidentification of the specimen.

The Confidentiality Agreement Form, while primarily focused on the non-disclosure of sensitive information, relates to the drug screening form in terms of handling personal and sensitive information. It underscores the importance of privacy and the ethical use of the data collected, similar to how the drug screen form includes measures to protect the donor's privacy and rights, such as sealing the specimen and requiring identification and consent. Both forms are essential in establishing trust and ensuring that information is used appropriately and only for its intended purpose.

Dos and Don'ts

When filling out the Federal Drug Testing Custody and Control Form, it's crucial to ensure the accuracy and integrity of the information provided. Below are essential do's and don'ts to consider:

Do:
  • Verify all personal information: Before submission, ensure that details like the SSN or Employee ID number, employer name, and address are correct.
  • Specify the testing authority clearly: Indicate the specific regulatory authority (e.g., DOT, HHS, NRC) overseeing the test to avoid any confusion.
  • Check the drug tests selected: Confirm that the correct drug tests (e.g., THC, COC, PCP) are marked according to the requirement.
  • Review collection site details: Make sure that the collection site name, code, address, and contact information are filled in accurately.
  • Ensure proper specimen handling: Confirm that the temperature is recorded correctly within the required timeframe, and all steps for specimen integrity (e.g., sealing, initialing) are meticulously followed.
Don't:
  • Leave sections blank: All fields, especially those requiring specific details (like the reason for the test and type of testing authority), must be completed.
  • Mislabel specimen bottles: Incorrectly labeling or failing to properly seal and initial the specimen bottles can lead to tests being invalidated.
  • Ignore remark sections: If there are deviations or observations during the collection or specimen handling, these must be noted in the remarks field as they could be critical for interpreting test results.
  • Overlook chain of custody: The chain of custody section is vital for the validity of the test. Skipping any part of this section could result in the sample being disqualified.
  • Forget to double-check for signatures and dates: Each step of the form that requires a signature or date must be duly filled out to affirm the accuracy and authenticity of the process.

Misconceptions

When it comes to drug screening in the workplace, there are several misconceptions that can muddy the waters for both employers and employees. Understanding the Federal Drug Testing Custody and Control Form is key to demystifying the process. Here are seven common misconceptions explained:

  • Privacy Invasion: Many believe that requiring a Social Security Number (SSN) or Employee ID on the form is an invasion of privacy. However, these identifiers are crucial for ensuring the confidentiality of the results and preventing mix-ups in the testing process.
  • One-Size-Fits-All Testing: There's a misconception that all drug tests screen for the same substances. The form clearly allows for specifying which drugs are to be tested for, including THC, COC, PCP, OPI, AMP among others, reflecting the tailored approach to meet specific regulatory or employer needs.
  • Random Tests Are Unregulated: The notion that random tests are arbitrarily conducted is false. The Drug Testing Form specifies different reasons for testing, including pre-employment, random, and reasonable suspicion, ensuring a regulated and fair process.
  • No Room for Error or Remarks: Some may mistakenly think there's no way to contest or annotate unusual circumstances during collection. However, the form has sections for remarks by the collector, and observations or issues can be officially recorded.
  • Immediate Dismissal Following a Positive Result: It's wrongly assumed that a positive drug test instantly leads to termination. The test form includes provisions for reconfirmation by a split testing laboratory, allowing for due process and verification of the initial results.
  • Adulterated Samples Go Unnoticed: Another misconception is that tampering with samples is easy and often goes undetected. The form allows the laboratory to report specimens as adulterated, substituted, or invalid, highlighting the rigorous checks in place to detect tampering.
  • Drug Screening Is Exclusively Punitive: Finally, many view drug screening purely as a punitive measure. While it's used to enforce regulations and safety, it also supports rehabilitation and return-to-work programs, noted in the form through the testing reasons like "Return to Duty" and "Follow-up."

Understanding these aspects of the drug screening process helps in appreciating its complexity and its role in maintaining a safe and compliant workplace. By demystifying these common misconceptions, both employers and employees can navigate the testing process more effectively, ensuring a fair and secure work environment.

Key takeaways

Filling out and using the Federal Drug Testing Custody and Control Form requires careful attention to detail to ensure accuracy and compliance with federal regulations. Here are key takeaways to remember during the process:

  • Ensure completeness of Step 1 by the collector or employer representative. This step is critical and involves recording essential details such as the employer's name, address, and identification number, along with selecting the specific Department of Transportation (DOT) agency under the testing authority, if applicable. Additionally, the reason for the test and the types of drugs being tested must be clearly indicated.
  • Accuracy in specimen handling is paramount. During Step 2, the collector must check the specimen's temperature within 4 minutes to ensure its validity. Additionally, whether the collection was observed, split, or single must be correctly recorded. Any discrepancies or unusual observations must be remarked upon in this section.
  • Proper sealing and initialing of the specimen bottle(s). In Step 3, it is crucial that the collector affixes the bottle seal(s) securely to the specimen bottle(s) and that the donor initials the seal(s) to confirm that the specimen is theirs. This step is a safeguard against tampering or specimen mix-up.
  • Chain of custody must be meticulously maintained. Step 4 outlines the initiation of the chain of custody by the collector, which is then completed by the testing facility. This section documents the handover of the specimen from the collector to the delivery service, ensuring that the specimen's integrity is maintained throughout the testing process.
  • Laboratory procedures for handling and analysis. Upon receiving the specimen at the laboratory, the accessioner must verify that the bottle seal is intact (Step 5A) and note any remarks if it is not. Following this, the certifying scientist performs the analysis and reports the findings, ensuring the process adheres to federal guidelines.
  • Documentation and confirmation of test results. In cases where a split specimen is used, Step 5b involves the reconfirmation of the test results by a split testing laboratory. This step adds an additional layer of verification to the original findings, supporting the accuracy and reliability of the overall testing process.

Throughout this process, it is essential for all parties involved—employers, collectors, and laboratory personnel—to adhere strictly to the guidelines and procedures outlined in the Federal Drug Testing Custody and Control Form. This ensures the validity and legal defensibility of the drug testing process.

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