DEA Proposes New Rule: Propionyl Chloride To Become a Controlled Chemical Estimated reading time: 3–5 minutes The Drug Enforcement Administration (DEA) is planning to make a new rule about propionyl chloride. This chemical is often used to make fentanyl and related dangerous drugs. The proposed rule would list propionyl chloride as a List I chemical. This means it will be controlled under the Controlled Substances Act (CSA). Why Is Propionyl Chloride Being Controlled? Propionyl chloride is used by illegal labs to make fentanyl, fentanyl analogues, and fentanyl-like substances. These drugs have caused many overdose deaths in the United States. Fentanyl is a powerful synthetic opioid. A small amount can be deadly. The DEA says propionyl chloride is important in making these drugs because it replaces another controlled chemical, propionic anhydride, during the process. What Will Happen If the Rule Is Finalized? Everyone who makes, sells, imports, or exports propionyl chloride will have to follow CSA rules. There will not be a threshold amount. This means any amount of propionyl chloride, even a tiny amount, will be regulated. Chemical mixtures that contain any propionyl chloride will also be regulated, no matter the concentration. No automatic exemptions will be given, but companies can apply for an exemption. Comment Period Open Until July 3, 2025 The DEA is asking for comments from the public about this rule. Comments need to be sent in by July 3, 2025. People can comment online at www.regulations.gov or by mail. All comments become part of the public record, so personal information could be seen by others. How Does Propionyl Chloride Make Fentanyl? Fentanyl and related drugs are not found in nature. They are made from chemicals. Propionyl chloride is used in several steps of different methods for making fentanyl. These methods include the “Janssen,” “Siegfried,” and “Gupta” processes. In these, propionyl chloride reacts with other chemicals to make important fentanyl building blocks. Illegal labs use propionyl chloride because it is easy to get and is not currently regulated. Making it a List I chemical will make it harder for illegal labs to get the chemical. Information Gathered by the DEA The DEA got six public comments about this action. Three comments supported the rule. Three others mentioned possible problems. Some said that propionyl chloride can also be used in research labs or in making pharmaceutical or agricultural products. Some worried that controlling this chemical would make it harder and more expensive for researchers to get. Others said most people who use it already have the paperwork to buy it. What Will Be Required If the Rule Takes Effect? Registration: Anyone making, selling, importing, or exporting propionyl chloride (or mixtures with it) must register with the DEA. Records and Reports: Records of transactions must be kept for two years. Any odd transactions, losses, or thefts must be reported. Shipping: Importing or exporting must follow DEA rules. Security: Companies must provide strong controls to prevent theft or misuse. Inspections: The DEA can inspect businesses handling this chemical. Legal Risk: Doing anything with propionyl chloride that is not allowed by law is a crime. There will be a temporary 30-day exemption for people already handling propionyl chloride. During this time, they must apply for registration or exemption. Economic and Legal Effects The DEA does not expect this rule to have big costs for companies. The main cost will be registration fees ($3,699 for manufacturers and $1,850 for distributors, importers, and exporters). Companies already making opioid medicines with fentanyl should already have DEA registration. The DEA thinks very few businesses will be impacted. The rule follows all proper government and legal procedures. It does not interfere with state laws or other government powers. Next Steps The DEA is taking comments until July 3, 2025. After that, they will decide if the rule should go into effect. Contact Information For more details, contact Terrence L. Boos at the DEA (571) 362-3249. How To Comment Online: www.regulations.gov (Docket No. DEA-1189) Mail: Drug Enforcement Administration, Attn: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, VA 22152 All comments must be sent or postmarked by July 3, 2025. Legal Disclaimer This article is for informational purposes only and does not constitute legal advice. For case-specific consultation, please contact us. Read our full Legal Disclaimer, which also includes information on translation accuracy.

DEA Proposes Rule to Place 4-Fluoroamphetamine in Schedule I Estimated reading time: 3–5 minutes On June 3, 2025, the Drug Enforcement Administration (DEA) announced a proposed rule to place the substance 4-fluoroamphetamine (4-FA) in Schedule I of the Controlled Substances Act (CSA). What Is 4-Fluoroamphetamine (4-FA)? 4-FA is a central nervous system stimulant. It is similar to amphetamine and methamphetamine, which are already controlled substances. 4-FA has no approved medical use in the United States. Why Is the DEA Proposing This Rule? This proposal is partly to help the United States meet its requirements under the 1971 Convention on Psychotropic Substances. The United Nations international body placed 4-FA in Schedule II of its convention in 2018. The DEA is acting to control 4-FA following these international decisions and U.S. law. What Evidence Did the DEA Review? The DEA and the Department of Health and Human Services (HHS) reviewed scientific studies, medical information, case reports, and law enforcement data. Their findings show that 4-FA: Acts like powerful stimulant drugs. Is being abused in the United States and elsewhere. Is found in illegal drug markets. Can cause serious health problems, including death. Has no accepted medical use. Details From the Scientific Review 4-FA produces effects similar to those of schedule I and II drugs such as amphetamine, methamphetamine, cocaine, and MDMA. It increases levels of certain chemicals in the brain and produces feelings of euphoria and high energy. People have taken it without medical advice, and it has been abused in many states. Law enforcement tested drug samples and found 269 reports of 4-FA in drug exhibits from January 2011 to December 2023. Most users are young adults. The drug can be taken by swallowing or snorting. 4-FA has caused emergency department visits, overdoses, and at least five deaths. Common effects include fast heartbeat, high blood pressure, headache, agitation, and fever. No studies show that it has accepted medical use or that it is safe for use with medical supervision. Proposed Rule Details If the rule is finalized, 4-FA will become a Schedule I controlled substance. This means: Only DEA-registered persons can manufacture, distribute, import, export, research, or possess 4-FA. Those who wish to handle 4-FA will need DEA registration. Those who do not register must surrender or transfer their 4-FA stock. 4-FA will need to be stored securely. Quotas will limit manufacturing. Inventories must be taken and records kept. Reports must be submitted to the DEA. Order forms must be used for transactions. Import and export rules will apply. Activities with 4-FA not allowed under the law may lead to criminal, civil, or administrative penalties. Comment Period and Hearing Requests Comments about the proposed rule must be submitted to the DEA by July 3, 2025. People may also request a hearing by that date, showing their interest and objections. Regulatory Effects This proposal will not have a big economic impact on small businesses. There is no evidence of legitimate use for 4-FA, except in some scientific research. The DEA says this rule does not add new paperwork requirements for businesses or government agencies, but existing recordkeeping rules must be followed. How to Comment Comments can be sent electronically through the Federal eRulemaking Portal at www.regulations.gov. Paper comments can be mailed to the DEA in Springfield, Virginia. All comments are part of the public record unless marked as confidential. Conclusion The DEA is proposing full control of 4-FA due to high potential for abuse and no accepted medical use. If the rule becomes final, 4-FA and related substances will be placed in Schedule I and subject to strict regulations. Legal Disclaimer This article is for informational purposes only and does not constitute legal advice. For case-specific consultation, please contact us. Read our full Legal Disclaimer, which also includes information on translation accuracy.

DEA Corrects Rule to Add 2-Methyl AP-237 to Schedule I Estimated reading time: 1–7 minutes On June 3, 2025, the Drug Enforcement Administration (DEA) issued a correcting amendment in the Federal Register. This update concerns the controlled substance 2-methyl AP-237. What is 2-methyl AP-237? 2-methyl AP-237 is a synthetic drug. Its full name is 1-(2-methyl-4-(3-phenylprop-2-en-1-yl)piperazin-1-yl)butan-1-one. It belongs to a group of drugs called synthetic opioids. These drugs can be changed in small ways in a lab to make similar versions. Why was there a correction? The DEA first published a final order on March 15, 2024. This order put 2-methyl AP-237 and its related chemical forms into Schedule I of the Controlled Substances Act. Schedule I drugs are thought to have a high chance for abuse and no approved medical use. The order said this new rule would start 30 days later, on April 15, 2024. Before this date came, the DEA published another rule about three different drugs. These drugs—etodesnitazene, N-pyrrolidino etonitazene, and protonitazene—were also put into Schedule I. Because these two rules overlapped, there was a mistake in the text about how 2-methyl AP-237 should be listed. What does the correction do? The correction fixes the list in the government rules. It adds 2-methyl AP-237 to 21 CFR 1308.11(b), which is the official list for Schedule I drugs. It also adds its special drug code number, 9664. All other parts of the rule stay the same. The correction says 2-methyl AP-237 has been in Schedule I since April 15, 2024. The change in the text does not change when the rule started. How does this affect the law? Since April 15, 2024, it has been illegal to make, sell, or have 2-methyl AP-237 without special permission. This applies to the drug and any chemical forms that are possible. Who signed this correction? The correction was signed on May 27, 2025, by DEA Acting Administrator Robert J. Murphy. Heather Achbach, DEA Federal Register Liaison Officer, submitted the document for publication. Where can you get more information? Questions can go to Dr. Terrence L. Boos at the DEA Drug and Chemical Evaluation Section. The phone number is (571) 362-3249. Summary 2-methyl AP-237 is now clearly listed as a Schedule I controlled substance. The rule has been effective since April 15, 2024. The correction fixes a technical mistake and makes the listing official and clear. Legal Disclaimer This article is for informational purposes only and does not constitute legal advice. For case-specific consultation, please contact us. Read our full Legal Disclaimer, which also includes information on translation accuracy.

Department of Justice Issues Notice on Immigration Court Forms Estimated reading time: 1–3 minutes The Department of Justice (DOJ) has published a notice about its collection of information for two important forms. These forms are used in immigration cases. The forms are called EOIR-60 and EOIR-61. The forms let an attorney or representative help a person, called a “pro se respondent,” with a legal document for the Board of Immigration Appeals or the Immigration Court. This is called a “limited appearance.” It means the lawyer only helps with one document. EOIR-60 is for the Board of Immigration Appeals. EOIR-61 is for the Immigration Court. Starting in July 2024, people can file these forms online using the EOIR Courts and Appeals System Respondent Access Portal (RAP). The forms have been updated. They no longer need to be mailed only. The EOIR Policy Manual now gives filing instructions. The new forms also let people show if they sent the paperwork to the other side electronically through ECAS. A change was made to the privacy notice on the forms. The correct system of records is JUSTICE/EOIR-003. More case information is now available online in English or Spanish at the EOIR Automated Case Information System. The EOIR-60 form now has a note to say that “limited appearance” is not allowed in Department of Homeland Security (DHS) proceedings that the Board controls. The DOJ asks for comments about the forms. People have 60 days, until August 4, 2025, to respond. They can give thoughts on whether the forms are needed, if the estimates of time are correct, and how to make the process easier. Here are details about the information collection: Type of Collection: The DOJ is updating and extending forms already in use. Forms: EOIR-60 (Board of Immigration Appeals) and EOIR-61 (Immigration Court). Who Fills Them Out: Individuals, attorneys, and representatives helping pro se respondents. Filling out the form is required to help with a document. Estimate of Use: About 40 people will fill out EOIR-60 each year. About 22,018 will fill out EOIR-61 each year. Time to Complete: Each form takes about 6 minutes. Total Annual Burden: 2,206 hours for everyone together. Cost: There is no fee to send in the forms. Forms can be sent online, saving postage costs. The estimated cost for a legal expert to fill out the form is $7.27 per time. The yearly cost for everyone combined is about $160,310.02. The DOJ’s contact for more information is Justine Fuga, Associate General Counsel at EOIR. People can also contact Darwin Arceo, Department Clearance Officer, for other questions. The notice was published on June 3, 2025. It is a public invitation for feedback on these forms and their collection. Legal Disclaimer This article is for informational purposes only and does not constitute legal advice. For case-specific consultation, please contact us. Read our full Legal Disclaimer, which also includes information on translation accuracy.

Department of Justice Requests Public Comment on DEA Registration Forms Estimated reading time: 3–5 minutes On June 3, 2025, the Department of Justice (DOJ) announced a request for public comments regarding an extension of an information collection. This collection is for the Drug Enforcement Administration (DEA) registration forms. The specific forms are DEA Form 225, DEA Form 225a for renewals, and DEA Form 225b for chain renewals. The DOJ is required to obtain approval from the Office of Management and Budget (OMB) before continuing to collect this information. They must do this under the Paperwork Reduction Act of 1995. The DOJ invites public comments for 30 days, ending July 3, 2025. The public may comment on the accuracy of time estimates for the forms, suggest better ways to collect information, and more. Anyone interested can provide comments online by visiting www.reginfo.gov/public/do/PRAMain. People may search for this collection using the title or OMB Control Number 1117-0012. The forms are used as part of the Controlled Substances Act. All businesses and individuals that manufacture, distribute, import, export, research, or analyze controlled substances must register with the DEA. These records keep controlled substances secure and ensure only approved people handle them. Here are the key details: Type of Collection: Extension, without changes, of a current approval. Title: Application for Registration, Registration Renewal, Affidavit for Chain Renewal. Forms: DEA 225, 225a, 225b. Affected Groups: Businesses, not-for-profit institutions, and government agencies. Number of Respondents: 16,560 per year. Estimated Time Per Response: 0.20066 hours. Frequency: Once per year. Total Annual Time Burden: 3,323 hours. Total Annual Non-Labor Cost: $0. Obligation: Required for businesses or individuals wanting to handle controlled substances. Anyone with questions or requests for copies of the forms or instructions can contact Heather E. Achbach, Regulatory Drafting and Policy Support Section, DEA. The contact address is 8701 Morrissette Drive, Springfield, Virginia 22152, telephone (571) 776-3882, or by email. For more information, the public can contact Darwin Arceo, Department Clearance Officer, at the DOJ’s Justice Management Division in Washington, DC. This information collection will stay in effect for up to three years if approved. Renewals will occur as needed for continued authorization. Legal Disclaimer This article is for informational purposes only and does not constitute legal advice. For case-specific consultation, please contact us. Read our full Legal Disclaimer, which also includes information on translation accuracy.

ANI Pharmaceuticals Inc. Applies to Import Controlled Substances Estimated reading time: 1–7 minutes ANI Pharmaceuticals Inc. has asked the Drug Enforcement Administration (DEA) to approve its registration as an importer of two controlled substances: Levorphanol and Tapentadol. Levorphanol has a drug code of 9220 and is listed as a Schedule II substance. ANI Pharmaceuticals plans to import Levorphanol for distribution to customers. Tapentadol has a drug code of 9780 and is also a Schedule II substance. ANI Pharmaceuticals will only import small amounts of Tapentadol. The Tapentadol is for internal research and making reference standards. No other uses of these drugs are allowed under this registration. Only bulk manufacturers already registered for these drugs, or new applicants, may send comments or objections about ANI’s application. Comments and objections must be sent electronically through the Federal eRulemaking Portal at https://www.regulations.gov. The deadline is July 2, 2025. Anyone asking for a hearing about this application must send their written request by July 2, 2025. Requests for hearings must be sent to several DEA addresses in Springfield, Virginia. These addresses include the Hearing Clerk/OALJ, the DEA Federal Register Representative/DPW, and the Administrator. The DEA says it will approve permit applications only if ANI Pharmaceuticals’ business activity matches what is allowed under U.S. law 21 U.S.C. 952(a)(2). ANI’s authorization will not cover importing FDA-approved or non-approved finished dosage forms for sale. The notice was signed by Matthew Strait, Deputy Assistant Administrator, and published in the Federal Register on June 2, 2025. Legal Disclaimer This article is for informational purposes only and does not constitute legal advice. For case-specific consultation, please contact us. Read our full Legal Disclaimer, which also includes information on translation accuracy.

Veranova, L.P. Applies to Manufacture Controlled Substances in Bulk Estimated reading time: 2–3 minutes Veranova, L.P. has sent an application to the Drug Enforcement Administration (DEA) to become a bulk manufacturer of several controlled substances. The request was made on April 17, 2025. The proposed location for manufacturing is 25 Patton Road, Pharmaceutical Service, Devens, Massachusetts 01434-3803. The company seeks to produce the following basic classes of controlled substances: Lysergic Acid Diethylamide (LSD) (Drug Code 7315), Schedule I 3,4-Methylenedioxymethamphetamine (MDMA) (Drug Code 7405), Schedule I Dimethyltryptamine (Drug Code 7435), Schedule I Amphetamine (Drug Code 1100), Schedule II Methylphenidate (Drug Code 1724), Schedule II Nabilone (Drug Code 7379), Schedule II Hydrocodone (Drug Code 9193), Schedule II Levorphanol (Drug Code 9220), Schedule II Thebaine (Drug Code 9333), Schedule II Alfentanil (Drug Code 9737), Schedule II Remifentanil (Drug Code 9739), Schedule II Sufentanil (Drug Code 9740), Schedule II The DEA states that Veranova plans to use the substances to support manufacturing and analytical testing at its other DEA-registered manufacturing facility. No other activities for these drug codes are authorized under this registration. Anyone who is a registered bulk manufacturer of these drugs, or is applying to become one, can submit comments or object to the proposed registration. Comments and objections must be sent electronically by August 1, 2025. To submit a comment, visit https://www.regulations.gov and follow the instructions. Once a comment is submitted, you will get a Comment Tracking Number as proof. Comments may not appear immediately online. A written request for a hearing about this application must also be filed by the deadline. This notice was signed by Matthew Strait, Deputy Assistant Administrator at the DEA. The official notice is document number 2025-09929 and was published in the Federal Register Volume 90, Number 104, on June 2, 2025. Legal Disclaimer This article is for informational purposes only and does not constitute legal advice. For case-specific consultation, please contact us. Read our full Legal Disclaimer, which also includes information on translation accuracy.

U.S. Marshals Service Proposes Extension of Sequestered Juror Information Form Estimated reading time: 2–3 minutes On May 28, 2025, the U.S. Marshals Service (USMS) at the Department of Justice announced a proposed extension for the “Sequestered Juror Information Form” in the Federal Register (Vol. 90, No. 101, p. 22515). This notice relates to collecting information from people or households as part of the USMS’s duty to keep federal courthouses, courtrooms, and judges safe. The “Sequestered Juror Information Form” (Form USM-523A) helps Marshals Service workers plan for and react to safety needs for jurors during court cases. There will be no changes to the form compared to the currently approved version. The USMS is simply asking for an extension of the form’s use. Comments about this extension are welcome for 60 days, ending on July 28, 2025. The public or other agencies can send feedback on things such as: Whether this information collection is needed for the job of the Bureau of Justice Statistics. If the estimate for time spent and the way it is counted is correct. How the quality or understanding of the questions can be improved. How to reduce the amount of time people need to spend answering. The USMS expects about 14 people to fill out this form each year. It should take each person about 4 minutes to finish. This adds up to around 1 hour total for all 14 people each year. There is no cost burden listed for the people filling out the form. If anyone wants to send comments, give suggestions, or get more information about the form or the process, they can contact Assistant Chief Karl Slazer at the USMS Headquarters in Arlington, Virginia at 703-740-2316 or by email. For further questions, Darwin Arceo, Department Clearance Officer, can be reached at the Justice Management Division in Washington, DC. The notice was dated May 21, 2025, and signed by Darwin Arceo as the Department Clearance Officer for the Paperwork Reduction Act at the U.S. Department of Justice. Legal Disclaimer This article is for informational purposes only and does not constitute legal advice. For case-specific consultation, please contact us. Read our full Legal Disclaimer, which also includes information on translation accuracy.

U.S. Marshals Service Requests Comments on Expedited Clearance Form Estimated reading time: 3–5 minutes The U.S. Marshals Service (USMS) is asking for public comments on an information collection form. The request is published in the Federal Register, Volume 90, Issue 101, dated Wednesday, May 28, 2025. The form is called “Leased/Charter/Contract Personnel Expedited Clearance Request.” It is also known as Form USM-271. The form is used to get and use contract flight personnel, such as pilots, cabin crew, and mechanics. These people are needed for short-notice flight missions for JPATS (Justice Prisoner & Alien Transportation System). The form collects information needed to complete quick background checks on flight staff. This helps keep U.S. Marshals Service and Bureau of Prisons prisoners safe during transport. Details of the Information Collection Type: Extension without change of a currently approved collection. Form Number: USM-271. Who Fills Out the Form: Individuals or households, such as contracted flight personnel. Number of Respondents: 180 estimated each year. Time to Complete: About 5 minutes per person. Total Time for All Respondents: 15 hours per year. USMS calculates the total time by multiplying 180 respondents by 5 minutes each, then dividing by 60 minutes for hours. How to Send Comments The USMS wants comments about four main points: If the information collected is needed for the Bureau of Justice Statistics and if it is useful. Whether the agency’s estimate of the burden is correct. If the collection can be made higher quality, more useful, or clearer. How to lessen the burden, such as using electronic or other modern technology. Comments will be accepted for 60 days, ending July 28, 2025. Contact for More Information If you want to send comments or need a copy of the form or instructions, contact: Assistant Chief Karl Slazer Management Support Division US Marshals Service Headquarters 1215 S Clark St., Ste. 10017 Arlington, VA 22202-4387 Phone: 703-740-2316 Email: [provided in the source document] If you need more information, you can also contact Darwin Arceo, Department Clearance Officer, United States Department of Justice, Justice Management Division, Policy and Planning Staff, Two Constitution Square, 145 N Street NE, 4W-218, Washington, DC. Official Notice This notice is signed by Darwin Arceo, Department Clearance Officer for PRA, U.S. Department of Justice, dated May 21, 2025 (FR Doc. 2025-09520). Legal Disclaimer This article is for informational purposes only and does not constitute legal advice. For case-specific consultation, please contact us. Read our full Legal Disclaimer, which also includes information on translation accuracy.

Department of Justice Announces First Meeting of Religious Liberty Commission Estimated reading time: 5–7 minutes The United States Department of Justice (DOJ) has announced the first meeting of the Religious Liberty Commission. The meeting will take place on June 16, 2025, from 9:00 a.m. to 4:00 p.m. The event will be held at the World Stage Theater, Museum of the Bible, located at 400 4th St. SW, Washington, DC 20024. The meeting will be recorded and broadcast at justice.gov/live. The Religious Liberty Commission was created by the President through Executive Order 14291. The Commission serves as a federal advisory committee. It has a chairperson, a vice chair, and eleven other members. These members are chosen by the President. They include people from the private sector, employers, schools, religious groups, and state governments. The Commission will give advice to the Domestic Policy Council and the White House Faith Office about religious liberty policies in the United States. It will also create a report for the President. This report will cover the history of religious liberty in America, how religious liberty has helped society, today’s threats to religious liberty, ideas on how to protect religious liberty, and programs to increase awareness and celebrate religious pluralism in America. At the first meeting, the Commission will discuss the history of religious liberty in America. The group will talk about the Founders’ plans to protect religious liberty in the First Amendment. They will also discuss how the Supreme Court has decided cases about religious liberty, mainly from the mid-twentieth century onward. The meaning of the separation of church and state will also be a topic. Anyone who wants to attend in person needs to register. In-person attendance is open to the first 300 people who sign up. People can register by sending their full name, organization (if there is one), and email address to the provided email address. All guests must show ID and pass a security screening. People who want to give public comments can send them in writing. Comments must be sent by 5:00 p.m. on June 15, 2025. They can be sent by email or mailed to the Department of Justice, Office of the Associate Attorney General, 950 Pennsylvania Avenue NW, Room 5706, Washington, DC 20530. For more information or to ask for help attending the meeting, contact M. Ashleigh Bondoc, Acting Designated Federal Official for the Religious Liberty Commission, by email or phone at 771-220-9743. This meeting notice is given under the Federal Advisory Committee Act (5 U.S.C. 1001 et seq.). Dated May 22, 2025. Legal Disclaimer This article is for informational purposes only and does not constitute legal advice. For case-specific consultation, please contact us. Read our full Legal Disclaimer, which also includes information on translation accuracy.

Department of Justice Seeks Comments on OJJDP Feedback Form Extension Estimated reading time: 3–5 minutes On May 27, 2025, the Department of Justice (DOJ), Office of Juvenile Justice and Delinquency Prevention (OJJDP), released a notice in the Federal Register. The notice concerns a request for public comments about the extension of an information collection called the “OJJDP National Training and Technical Assistance Center (NTTAC) Feedback Form Package.” This collection is identified with OMB Number 1121-0277. The OJJDP is asking the public to send comments about whether the information collected is needed for its activities, the accuracy of the estimated time for people to respond, ways to make the data better, and methods to decrease the time it takes to complete the forms. Comments will be accepted for 60 days, until July 28, 2025. If you need more information or want to review the forms, you can contact Jill Molter, the Digital Communications and Training and Technical Assistance Coordinator at OJJDP’s NTTAC. She can be reached by phone at 202-514-8871 or by mail at 999 North Capitol Street NE, Washington, DC 20002. Comments can also be sent to the Office of Management and Budget at [email address protected]. The main purpose of the Feedback Form Package is to collect feedback from people who receive technical help, attend conferences, provide training, or take part in focus groups. This helps OJJDP and NTTAC check on the quality of their services, make needed changes, and improve training and help for people working in juvenile justice. The form will be sent to many groups, including individuals, households, all levels of government, non-profits, and private businesses. The process will help OJJDP learn about people’s satisfaction and understand their needs better. It is estimated that 4,756 people will fill out these forms. The time it takes to fill out a form could be as quick as 0.03 hours or as long as 1.5 hours. The total time for all responses in one year is expected to be about 430.5 hours. If additional information is needed, Darwin Arceo, Department Clearance Officer at the Justice Management Division, can be contacted at Two Constitution Square, 145 N Street NE, 4W-218, Washington, DC 20530. The notice was officially signed by Darwin Arceo on May 21, 2025. The Department of Justice encourages everyone involved or interested to share their comments before the deadline. Legal Disclaimer This article is for informational purposes only and does not constitute legal advice. For case-specific consultation, please contact us. Read our full Legal Disclaimer, which also includes information on translation accuracy.

Department of Justice Seeks Public Comment on Nonprofit Credit Counseling Agency Application Process Estimated reading time: 3–5 minutes The United States Department of Justice has issued a notice about changes to its Application for Approval as a Nonprofit Budget and Credit Counseling Agency. This notice comes from the United States Trustee Program. It appears in the Federal Register, Volume 90, Number 100, dated Tuesday, May 27, 2025. The Department is asking for public comments. People can send comments until July 28, 2025. The reason for the notice is to change an information collection. The Department wants to make sure the application process for nonprofit credit counseling agencies works well and follows the law. These nonprofit agencies help people who want to file for bankruptcy. The Bankruptcy Abuse Prevention and Consumer Protection Act of 2005 (BAPCPA) says anyone filing for bankruptcy must, within 180 days before filing, get credit counseling from an approved nonprofit agency. The Application asks these agencies for information so that the Department of Justice can make sure they follow all the rules. There is no specific agency form number for this collection. The United States Trustee Program is the department in charge. The public group affected by this change is nonprofit agencies wanting to give credit counseling to bankruptcy filers. According to the notice, 74 agencies are expected to complete the application. The time it takes to finish this application is different for new and renewing agencies: Initial applicants need about 10 hours. Standard renewal applicants need about 4 hours. Refreshed renewal applicants need about 9 hours. The Department estimates the total burden for all agencies is about 391 hours. People who want more information or wish to see the full application form can contact Juliet Drake at the United States Trustee Program. Contact details include the address (441 G Street NW, Suite 6150, Washington, DC 20548), email, and phone number (202-307-3698). Further questions can also be sent to Darwin Arceo, the Department Clearance Officer, at the Department of Justice, Justice Management Division, Two Constitution Square, 145 N Street NE, 3E.405A, Washington, DC 20530. The Department encourages everyone to look at how the information collection works. The public is asked to give thoughts on: If collecting this information is needed for the Trustee Program to work well. Whether the agency’s time estimates for filling out the forms are right. How the collection could be made more clear and useful. Ways to make the process easier, like using technology. Written by order of Darwin Arceo, Department Clearance Officer for the Paperwork Reduction Act, U.S. Department of Justice. The notice was filed on May 23, 2025. Legal Disclaimer This article is for informational purposes only and does not constitute legal advice. For case-specific consultation, please contact us. Read our full Legal Disclaimer, which also includes information on translation accuracy.

Department of Justice Seeks Comments on Financial Course Provider Application Estimated reading time: 2–4 minutes What Is Happening? The Department of Justice is asking the public to send comments about this application. The public can send comments until July 28, 2025. Who Can Comment? Anyone who is interested, especially those who want to give feedback about how much work the application is, how much time it takes, how useful it is, and how it could be better. Suggestions for using technology, like electronic forms, are also welcome. Who Fills Out This Application? Individuals and businesses who want to teach personal financial management to debtors in bankruptcy cases must fill out this application. The application is required by the Bankruptcy Abuse Prevention and Consumer Protection Act of 2005. Debtors must complete an approved instructional course before they can have their debts discharged. What Information Does the Application Collect? The application gathers information from potential course providers to make sure they meet legal requirements and rules. Providers must follow the criteria set by the United States Trustee Program. How Long Will It Take? There will be about 135 respondents. First-time applicants will spend about 10 hours to complete the application. Standard renewal applicants will spend about 4 hours. Applicants doing a special type of renewal will spend about 9 hours. Additional Surveys for Debtors About 468,238 debtors are expected to fill out a survey about the instructional course. This survey should take about 1 minute to finish. Total Time Needed Each Year The total time spent by applicants will be about 694 hours. The total time spent by debtors will be about 7,804 hours. The total public burden is estimated at 8,498 hours every year. How to Get More Information For more about the application and instructions, contact Juliet Drake, Deputy Assistant Director, Executive Office for United States Trustees, at 441 G Street NW, Suite 6150, Washington, DC 20548, or call (202) 307-3698. If more information is needed about the collection process, contact Darwin Arceo, Department Clearance Officer, U.S. Department of Justice, at 145 N Street NE, 3E.405A, Washington, DC 20530. Important Dates Comments must be submitted by July 28, 2025. Document Details This notice was published in the Federal Register on May 27, 2025, under document number 2025-09473. Legal Disclaimer This article is for informational purposes only and does not constitute legal advice. For case-specific consultation, please contact us. Read our full Legal Disclaimer, which also includes information on translation accuracy.