FR 2025-01958

Overview

Title

Agency Information Collection Activities; Proposed eCollection eComments Requested; Extension Without Change of a Previously Approved Collection; The National Forensics Laboratory Information System Collection of Analysis Data

Agencies

ELI5 AI

The Department of Justice wants to keep checking how drugs are tested in labs to make sure they get the info right, and they're asking for permission to keep doing this from people who make the rules. They're also asking people to say if they think it's a good idea, but there are some confusing things about how much work it takes and how it helps, so they need better explanations.

Summary AI

The Department of Justice, specifically the Drug Enforcement Administration (DEA), announced a notice for public commentary on its information collection request related to the National Forensics Laboratory Information System. This system gathers drug analysis data from non-federal labs to improve accuracy on drug information. The DEA is seeking approval from the Office of Management and Budget (OMB) for a three-year extension without changes to the existing collection, which involves responses from various agencies and businesses. Public comments on the burden and utility of this data collection are being accepted until March 3, 2025.

Abstract

The Department of Justice (DOJ), Drug Enforcement Administration (DEA), will be submitting the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995.

Type: Notice
Citation: 90 FR 8534
Document #: 2025-01958
Date:
Volume: 90
Pages: 8534-8535

AnalysisAI

The document outlines a notice from the Department of Justice (DOJ), particularly the Drug Enforcement Administration (DEA), concerning the continuation of a data collection initiative related to the National Forensics Laboratory Information System. This system is crucial for accumulating drug analysis data from non-federal laboratories across the country. It aims to create a centralized and updated repository for drug-related information, useful for various stakeholders in the field of drug enforcement and policy-making. The DEA is seeking a three-year reauthorization of this initiative without any changes to its current format. As part of the process, the public is invited to comment on aspects such as the practicality and utility of this data collection, its burden on respondents, and the methods used for estimation.

One significant issue with the document is the discrepancy in the estimated annual time burden for respondents. Initially reported as 4,860 hours in a previous notice, it has now been corrected to 1,860 hours, but with no explanation for the earlier error or the correction. This inconsistency potentially undermines the reliability of the document and raises questions about the accuracy of the data collection process.

Another concern is the lack of a clear explanation of the obligation to respond, which is stated as "Required to Obtain or Retain Benefits." This phrase suggests there are benefits linked to participation, but these benefits are not clearly defined in the document. This ambiguity may create confusion for the entities required to respond, who may not fully understand the incentives or requirements involved.

Additionally, the methodology for estimating the time each respondent will spend and the frequency of responses is not detailed. A better understanding of how these estimates were calculated would not only enhance the transparency of the process but also provide reassurance to those affected that the burdens of participation are reasonable and justified.

Although the document states that there are no estimated annual other costs associated with this data collection, it does not address potential indirect costs. These could include the administrative or operational impacts on participating entities, especially for smaller organizations that might struggle with additional burdens.

The continuation of this data collection initiative may have several broad impacts on the public. By centralizing drug analysis data, the DOJ aims to enhance the quality and availability of information on drug use and abuse patterns, contributing to more informed policy-making and law enforcement efforts. This could ultimately lead to more effective strategies for combating drug-related issues.

For specific stakeholders such as non-federal laboratories, the initiative comes with both positive and negative aspects. On one hand, their participation can contribute to a collective effort against drug problems, potentially leading to broader societal benefits. However, the requirement to provide data may impose some burdens, especially if the internal processes need to be adjusted to accommodate data collection and submission requirements.

Overall, while the document details a critical effort in drug enforcement information gathering, there are points that require further clarification to ensure the understanding and cooperation of all involved stakeholders. Addressing these issues would enhance the transparency and efficacy of this ongoing initiative.

Financial Assessment

The Federal Register document from the Department of Justice, specifically the Drug Enforcement Administration (DEA), provides details about a proposed information collection activity related to the National Forensics Laboratory Information System. Within this proposal, there is a particular focus on the financial reference found in the estimated costs associated with the activity.

Financial References

The document mentions the total estimated annual other costs burden being $0. This statement indicates that, according to the DEA's assessment, there are no additional financial expenditures directly associated with this information collection requirement. Essentially, the implication is that completing this data collection does not impose extra financial obligations on the participants beyond the time investment needed to comply.

Relation to Identified Issues

One of the identified issues in the document is the discrepancy in the total estimated annual time burden, which was initially listed as 4,860 hours and later corrected to 1,860 hours. While the financial section of the document does not directly discuss monetary costs beyond specifying them as zero, the time burden indicates an implicit cost. The reduction in the time burden figure could imply a more efficient process or a revised estimate of participants' efforts, which indirectly mitigates costs categorized under labor or productivity.

Moreover, the document identifies that the obligation to respond is necessary to obtain or retain benefits. However, it lacks explicit financial benefit details or definitions, leaving one to infer that the primary benefit of compliance is not financial savings or gains, but possibly operational or regulatory compliance benefits that hold intrinsic value to the respondents.

The absence of identified costs brings to light potential concerns regarding indirect expenses, such as those stemming from the time spent by the respondents, which are not quantified in dollar terms. This consideration is particularly crucial for smaller entities that might operate under resource constraints.

Conclusion

While the document maintains a stance of having no financial burden beyond time, the correction in the estimated hours presents an opportunity to re-evaluate and define any hidden, indirect costs that might affect the respondents. Enhancing the transparency of these financial evaluations would potentially aid stakeholders in understanding the full scope of their engagement's implications, enabling them to make informed decisions about their participation.

Issues

  • • The notice provides an incorrect number for the total estimated annual time burden, initially listed as 4,860 hours in the 60-Day notice, but corrected to 1,860 hours here without explanation of the discrepancy.

  • • The obligation to respond is listed as 'Required to Obtain or Retain Benefits,' but there is a lack of detailed explanation on how the benefits are defined or what specific advantages would be lost if not responded.

  • • The assumption used for the estimated time per respondent and frequency is not detailed, which might lead to questions about the methodology's validity. More transparency on these calculations would be beneficial.

  • • No estimated annual other costs burden is identified, yet there might be indirect costs associated with participation that aren't quantified in the document.

Statistics

Size

Pages: 2
Words: 989
Sentences: 45
Entities: 82

Language

Nouns: 322
Verbs: 73
Adjectives: 44
Adverbs: 9
Numbers: 57

Complexity

Average Token Length:
5.79
Average Sentence Length:
21.98
Token Entropy:
5.22
Readability (ARI):
20.14

Reading Time

about 3 minutes