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In the state of New Jersey, professionals and entities that intend to handle controlled dangerous substances are mandated to navigate through a regimented process, as outlined by the Office of the Attorney General, Division of Consumer Affairs, Drug Control Unit. This involves the completion and submission of the Controlled Dangerous Substance (C.D.S.) Registration form, a critical document designed to ensure that those manufacturing, prescribing, distributing, dispensing, or conducting research with these substances comply with state regulations. The form, which requires a meticulous $20.00 payment to the "State of New Jersey,” initiates a process that, while taking 4-6 weeks for approval, culminates in the issuance of a New Jersey specific C.D.S. registration. It should be noted that this registration is strictly valid within the state, underscoring New Jersey's commitment to maintaining strict oversight of controlled substances within its borders. Furthermore, the application process is comprehensive, demanding detailed information about the applicant, including licensure and previous interactions with controlled substances, across any jurisdiction. This reflects an overarching strategy to safeguard public health and safety, by ensuring that only qualified and responsibly vetted individuals or organizations gain the authorization to handle these potentially dangerous substances. Importantly, the document also highlights a harmonization of state requirements with federal mandates, by urging applicants with out-of-state D.E.A. registrations to either transfer or obtain a new registration for their practice in New Jersey, further emphasizing the layered scrutiny involved in managing controlled dangerous substances.

Sample - Nj Dangerous Substance Registration Form

New Jersey Ofice of the Attorney General

Division of Consumer Affairs

Drug Control Unit

124 Halsey Street, 3rd Floor, P.O. Box 45045, Newark, NJ 07101

(973) 504-6351

Controlled Dangerous Substance Registration

Instruction sheet

Enclosed is a Controlled Dangerous Substance (C.D.S.) application, which you are required to submit pursuant to N.J.S.A. 24:21-1 et seq. Registration is required for every person who, or irm that, manufactures, prescribes, distributes, dispenses or conducts research or

analysis utilizing controlled dangerous substances.

A New Jersey C.D.S. registration is issued only for a New Jersey location. Be sure to include a $20.00 check or money order,

payable to “State of New Jersey.” It will take 4-6 weeks to process this application. Your C.D.S. registration will be mailed to the mailing address on ile with your professional licensing board.

Please note:

1.If you have a current D.E.A. number in another state and plan to discontinue practice in that state, you may transfer that D.E.A. number to New Jersey by providing the following to the Drug Enforcement Administration, 80 Mulberry Street, Newark, New Jersey 07102, (888-356-1071) www.deadiversion.usdoj.gov:

a.a copy of your New Jersey professional license or a veriication letter from the licensing board;

b.a copy of your New Jersey C.D.S. registration or a veriication letter;

c.a copy of your out-of-state D.E.A. registration; and

d.a letter requesting an address change to the same address that is on your New Jersey C.D.S. registration.

A D.E.A. number is only valid in the state listed on the certiicate.

2.If you plan to practice in both New Jersey and the state(s) where you currently hold a D.E.A. registration(s), you must also obtain a D.E.A. registration for New Jersey. Please contact the D.E.A. at the address indicated above and complete the New Jersey application.

3.In order to complete the attached application, please note:

a.A dispenser/prescriber/ practitioner includes medical doctors, doctors of osteopathy, dentists, optometrists, veterinarians, and podiatrists. A mid-level dispenser/prescriber/practitioner includes physician assistants, advanced practice nurses and certiied nurse midwives. Pharmacies must complete a separate application.

b.Every person or irm handling controlled dangerous substances in New Jersey is required to have both a state and federal registration for that purpose. Federal facilities do not require registration.

c.The address supplied must be current and an actual location where controlled dangerous substances will be stored, prescribed, dispensed, etc. The address cannot be solely a post ofice box.

d.Dentists and optometrists may only register at the address for which they hold a current registration issued by their board and at which the C.D.S. registration is required pursuant to 3(c) above.

e.Individual practitioner applicants (medical doctors, dentists, veterinarians, etc.) must use their own name, not professional association/corporation or partnership information.

f.Pharmacies are required to use their common trading name (e.g. David Pharmacy), not a business or corporate name.

g.Dispensers/Prescribers must have an active and current New Jersey professional license number. Please write in your New

Jersey professional license number in “Section B” of the application.

Advanced Practice Nurses may prescribe controlled dangerous substances, but may not purchase or maintain any stock supplies of any C.D.S. medication.

Optometrists are authorized to prescribe/dispense only Schedule III, IV and V controlled substances and must have an O.M. number registered with their board.

4.If more space is required for your response to any question on the application, please submit a separate sheet of paper identifying the section(s) to which you are responding.

If we can be of further assistance, please call 973-504-6351.

6/08

New Jersey Is An Equal Opportunity Employer Printed on Recycled Paper and Recyclable

 

New Jersey Ofice of the Attorney General

 

Initial Application for Registration

 

Drug Control Unit

 

 

 

for Dispenser – Pharmacy

 

P.O. Box 45045

 

 

New Jersey Controlled Dangerous Substances Act

 

Newark, NJ 07101

 

 

 

 

 

 

N.J.S.A. 24:21-1 et seq.

 

 

 

 

 

 

Please type or print irmly with a ballpoint pen.

 

 

 

 

 

 

 

 

 

Section A:

All of the items in this section must be completed.

Section B:

Pharmacy Licensure Information

 

 

 

 

1. Provide the applicant’s name and the place of business to be registered (do

 

 

not use solely a P.O. box). registration will be provided for New Jersey

Pharmacy permit number _____________________________________

locations only. If the registration is for a University of Medicine and

 

 

Dentistry of New Jersey facility, include the department, room number,

 

 

 

designation, e.g. MEB, MSB, etc. The address of record must be your

Section C:

Business Information

practice location.

 

 

 

 

 

 

 

 

1. List the name, address and telephone number of the person who has

 

 

 

 

 

________________________________________________________

 

administrative or managerial responsibility for the registered location.

 

Pharmacy trade name

 

 

 

 

________________________________________________________

 

 

 

Last name

First name

MI

 

 

 

C.D.S. – Responsible Individual

 

 

 

 

________________________________________________________

 

 

 

 

Department

 

Room number

 

 

 

 

 

 

2. List the name, address and telephone number of the registered agent (if

 

 

 

 

 

________________________________________________________

 

a corporation) or the name and address of the New Jersey resident upon

 

Street address

 

 

 

 

 

whom process may be served (if a nonresident proprietor or partner).

 

 

 

 

 

________________________

New Jersey

__________________

 

 

 

 

City

 

ZIP code

 

 

____________________________ __________________________

 

 

 

Home telephone number (include area code)

Business telephone number (include area code)

 

 

Note: Please note that the above-registered address is subject to inspection pursuant to N.J.S.A. 24:21-31 & 32.

 

 

 

 

 

 

 

2. Registration requested as: Dispenser ($20)

 

 

 

 

Make the check or money order payable to: State of New Jersey

Section D:

Certiication

3. Registration requested in the following Schedule(s):

Schedule

II

III

IV

V

 

 

 

 

 

 

 

 

I, ______________________________________ being duly sworn,

4. (a) Has any restriction been imposed which would affect your privilege

depose and say under penalty of false statement, that I am the person

to hold a controlled dangerous substances (C.D.S.) registration for

Schedule II, III, IV or V substances in New Jersey, any other state,

described and identiied in this application; that the information given

the District of Columbia or in any other jurisdiction?*

 

in this application and all submitted materials contain no willful

 

 

 

 

Yes

No

 

 

 

 

misrepresentations and that the information is true and complete. I

 

 

 

 

 

 

(b) Have you been arrested, indicted or convicted of a crime in

understand that should an investigation at any time disclose otherwise,

connection with controlled substances under federal law or the laws

my application may be rejected, and I may face legal sanctions if I

of New Jersey, any other state, the District of Columbia or any other

am already registered. I understand that in signing this application for

jurisdiction?*

 

 

 

Yes

No

 

 

 

registration, I am consenting to any reasonable inquiry that may be

(c) Have you ever surrendered a controlled drug registration or had a

necessary to verify the information that I have provided on this form

controlled drug registration revoked, suspended or denied in New

or may provide in conjunction with this application.

Jersey, any other state, the District of Columbia or in any other

 

jurisdiction?*

 

 

 

Yes

No

 

(d) If the applicant is a corporation, association, or partnership: has any

 

oficer, partner, stockholder holding 10% or more of the outstanding shares

______________________________________

or employee who has access to controlled dangerous substances been

Applicant's full signature

convicted of a crime in connection with controlled substances under

 

federal law or the laws of New Jersey, any other state, the District of

 

Columbia or any other jurisdiction?*

 

Yes

No

 

(e) If the applicant is a corporation, association, or partnership: has any

______________________________________

oficer, partner, stockholder holding 10% or more of the outstanding

Date

shares or employee who has access to controlled dangerous substances

 

surrendered a controlled drug registration, had a controlled drug

 

registration suspended, revoked, or denied, or owned or worked

 

for an entity which has surrendered or had revoked, suspended, or

 

denied a controlled drug registration under federal law or the laws

 

of New Jersey, any other state, the District of Columbia or any other

 

jurisdiction?*

 

 

 

Yes

No

 

* If "Yes," attach a letter setting forth the circumstances of such action.

DDC-25

Revised 6/08

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

FOr StAte USe ONlY

C.D.S. number________________________

Effective date ___________________________ Expiration date ______________________

 

 

 

 

 

 

 

Retain the last copy for your records. Mail the remaining copies with your fee to the above address.

Document Specifications

Fact Name Description
Governing Law The New Jersey Controlled Dangerous Substances Act, N.J.S.A. 24:21-1 et seq., governs the process and requirements for the registration related to controlled dangerous substances in New Jersey.
Registration Requirement Every individual or firm that manufactures, prescribes, distributes, dispenses, conducts research, or analysis utilizing controlled dangerous substances in New Jersey must submit a Controlled Dangerous Substance (C.D.S.) application for registration.
State and Federal Registration Applicants handling controlled dangerous substances are required to have both a state (New Jersey) and a federal registration, except federal facilities which do not require state registration.
Application Fee and Processing Time An application fee of $20.00, payable to "State of New Jersey," is required. The processing of the application typically takes 4-6 weeks.

Detailed Steps for Using Nj Dangerous Substance Registration

To operate effectively and lawfully when managing controlled dangerous substances within New Jersey, obtaining a Controlled Dangerous Substance (C.D.S.) registration is a crucial step. This registration ensures compliance with N.J.S.A. 24:21-1 et seq., and is mandatory for individuals and firms across various professions—including healthcare providers and pharmacies—where the possession, prescribing, manufacturing, distribution, dispensation, research, or analysis of controlled substances is part of their operations. With this process generally taking between four to six weeks, ensuring accuracy and completeness in your application can facilitate smooth handling. A non-refundable fee of $20.00 is required, payable to “State of New Jersey.” The forthcoming instructions lay out a clear pathway to complete your C.D.S. registration application methodically.

  1. Preparation: Before filling out the form, gather all necessary information including your New Jersey professional license, a check or money order for the application fee, and any other relevant documents.
  2. Section A - General Information: Begin by providing your personal and business information as requested. Ensure that the address provided is the actual physical location related to the C.D.S. activities and not just a P.O. box.
  3. Section B - Pharmacy Licensure Information: For pharmacies, input your New Jersey Pharmacy permit number. This section is specific to pharmacies, so individual practitioners can skip this section.
  4. Section C - Business Information: List the details of the person with administrative or managerial responsibility for the C.D.S. at the registered location. Additionally, provide information about the registered agent or the New Jersey resident designated for process service, if applicable.
  5. Payment of Fee: Attach a check or money order for $20.00 made payable to “State of New Jersey.” This fee is non-refundable.
  6. Section D - Certification: The certification section must be completed by the applicant, indicating understanding and truthfulness of the information provided. Sign and date this section to confirm your compliance and consent.
  7. Review and Attach Additional Documents: Confirm all the information entered is accurate and complete. If more space was needed for any response, ensure the additional sheets are clearly labeled and attached. Moreover, if you answered "Yes" to any of the questions in Section D regarding legal issues or restrictions related to controlled substances, attach a detailed explanatory letter.
  8. Submission: Once all parts of the application are completed, retain a copy for your records and mail the remaining copies along with the application fee to the address provided on the form: New Jersey Office of the Attorney General, Drug Control Unit, P.O. Box 45045, Newark, NJ 07101.

After submitting your application, anticipate a processing time of four to six weeks. Keep in mind that your application is subject to review and verification, and additional information may be requested. Maintaining open communication lines with the New Jersey Drug Control Unit can help resolve any issues promptly, ensuring your registration is processed efficiently.

Learn More on Nj Dangerous Substance Registration

What is a Controlled Dangerous Substance (C.D.S.) registration and who needs it in New Jersey?

A Controlled Dangerous Substance (C.D.S.) registration is a mandatory requirement in New Jersey for individuals or entities that engage in the manufacture, prescription, distribution, dispensing, or research of controlled dangerous substances. This includes medical doctors, dentists, optometrists, veterinarians, podiatrists, physician assistants, advanced practice nurses, certified nurse midwives, and pharmacies. Anyone handling controlled dangerous substances within the state must obtain this registration to legally operate concerning these substances.

How do I apply for a C.D.S. registration in New Jersey?

To apply for a C.D.S. registration, complete the application provided by the New Jersey Office of the Attorney General, Division of Consumer Affairs, Drug Control Unit. Ensure all fields in Section A and the applicable parts of Section B and C are filled out correctly. Dispensers, prescribers, and practitioners should include their New Jersey professional license number in Section B. A fee of $20.00, payable by check or money order to the "State of New Jersey," must accompany your application. It's important to provide a current physical address, as P.O. Boxes are not accepted.

Can I transfer my D.E.A. registration from another state to New Jersey?

  1. If you possess a D.E.A. number in another state and intend to cease practice there, you may transfer your D.E.A. number to New Jersey. You need to provide the Drug Enforcement Administration in Newark, New Jersey, with your New Jersey professional license or a verification letter, a copy of your New Jersey C.D.S. registration, your out-of-state D.E.A. registration, and a letter requesting an address change to match your New Jersey registration.
  2. If you wish to practice in New Jersey and retain your D.E.A. registration in another state, you must obtain a separate D.E.A. registration for New Jersey.

What should I do if I need more space to complete a section on the application?

If the space provided on the application is insufficient for your responses, you are encouraged to attach a separate sheet of paper. Ensure that you clearly identify the section of the application your additional information pertains to. This helps maintain the organization of your application and assists in the review process.

Common mistakes

When completing the New Jersey Dangerous Substance Registration Form, individuals often encounter pitfalls that could delay or complicate their registration process. Here are nine common mistakes to avoid:

  1. Not Including the Fee: Failing to attach a check or money order for $20.00 payable to "State of New Jersey" can result in an incomplete application process.
  2. Using Outdated Information: Providing an address that is no longer current or is not an actual location where controlled dangerous substances will be handled is a critical error.
  3. Listing a P.O. Box as the Address: The form clearly indicates that a post office box cannot serve as the business or practice address. This stipulation is often overlooked.
  4. Incorrect Entity Name Use: Individual practitioners must use their own name rather than a professional association, corporation, or partnership name. Pharmacies must use their trading name.
  5. Omitting New Jersey Professional License Number: Not writing the New Jersey professional license number in “Section B” of the application can lead to delays in processing.
  6. Misunderstanding Dispenser Authorization: Advanced Practice Nurses may prescribe but cannot purchase or maintain stock supplies of controlled dangerous substances, which is often misunderstood or overlooked.
  7. Not Requesting Additional Space Properly: If additional space is needed for responses, a separate sheet must be submitted with the relevant section(s) identified. This requirement may be missed, leading to incomplete answers.
  8. Incorrect Schedule Selection: Not correctly requesting registration in the appropriate schedule(s) II, III, IV, or V for controlled substances can lead to processing issues.

Addressing these common mistakes before submitting the New Jersey Dangerous Substance Registration Form ensures a smoother review process by the Drug Control Unit. Ensuring accuracy and completeness of all entered information is paramount. The document is critical for those handling controlled dangerous substances within New Jersey, and as such, it deserves careful and thorough preparation.

Documents used along the form

When dealing with the New Jersey Dangerous Substance Registration form, numerous additional documents and forms are frequently utilized to ensure compliance with regulatory requirements. These documents cover a range of needs, from verifying the identity and credentials of the applicant to detailing specifics about the substances they intend to handle.

  1. Professional License Verification: This document proves the applicant holds a valid professional license in New Jersey, relevant for medical doctors, dentists, veterinarians, etc., as required by the Dangerous Substance Registration process.
  2. DEA Registration Transfer Documentation: For those already holding a DEA number in another state, documentation to transfer this number to New Jersey is required, including a current professional license and a request letter for the transfer.
  3. Controlled Substance Inventory Log: An essential document for maintaining a record of controlled substances, indicating quantities on hand, dates of acquisition or dispensing, and the names of suppliers and recipients.
  4. Background Check Authorization: Allows for the verification of an applicant’s criminal history to ensure no convictions related to controlled substances, an essential step in the vetting process for handling dangerous substances.
  5. Pharmacy or Facility Inspection Reports: Documents from inspections conducted at the premises where controlled substances will be stored or handled, ensuring compliance with storage and security regulations.
  6. Corporate or Business Entity Documentation: For applicants operating within a corporate or business entity, documents proving the legal status and structure of the entity may be needed, including information on officers or partners.
  7. Letter of Good Standing: From the New Jersey professional licensing board, confirming the applicant’s license is active, without any restrictions or sanctions, further emphasizing their eligibility to handle controlled substances.

Collectively, these documents complement the New Jersey Dangerous Substance Registration form by providing a comprehensive profile of the applicant and their operational setup. They ensure that all applicants meet the stringent criteria set forth for handling controlled dangerous substances, thereby safeguarding public health and safety.

Similar forms

The New Jersey Dangerous Substance Registration form shares similarities with the Federal DEA (Drug Enforcement Administration) Registration application. Both forms are essential for healthcare providers or entities that handle controlled substances, requiring them to obtain authorization before engaging in activities such as prescribing, dispensing, or distributing these substances. Each application mandates the provision of detailed information about the applicant's credentials, the location where controlled substances will be managed, and compliance with specific regulatory requirements. Furthermore, they both inquire about the applicant's history concerning controlled substances, including any past legal issues or disciplinary actions, thus ensuring that only qualified and compliant professionals and businesses are granted the privilege to work with these substances.

Comparable to the New Jersey Dangerous Substance Registration form, Pharmacy Permit applications issued by state boards of pharmacy require comprehensive details about the pharmacy's operations, the responsible pharmacist, and adherence to state regulations on controlled substances. These permit applications are designed to verify that pharmacies have the necessary infrastructure and oversight to safely handle and dispense controlled substances. They also focus on the verification of the pharmacist's credentials and their authority to operate within the state, mirroring the credential and practice site verification processes seen in the New Jersey Dangerous Substance Registration form.

Medical and Professional Licensing Applications also bear resemblance to the New Jersey form, particularly in their stringent assessment of qualifications and background. Just as the Dangerous Substance Registration form requires information about the healthcare professional's qualifications and right to handle controlled substances, licensing applications demand detailed evidence of education, training, and sometimes prior practice history. Both types of documents may include queries regarding disciplinary actions or criminal history to ensure the applicant's suitability for their professional responsibilities.

Similarly, the Controlled Substance Registration for Research Institutions, required for academic or research institutions that intend to use controlled substances for scientific research, parallels the New Jersey Dangerous Substance Registration form in several ways. Both necessitate details about the facility, the specific substances to be used, and the scope of their use. They also enforce strict regulatory compliance and background checks to prevent the misuse of controlled substances, whether in a clinical setting or research environment.

Finally, the Hazardous Waste Generator Registration forms, while focusing more broadly on hazardous materials rather than strictly on controlled substances, share the spirit of regulation and safety underscored by the New Jersey Dangerous Substance Registration form. These registrations require entities to provide operational details, emergency response plans, and waste disposal methods to ensure public and environmental safety. Similar to the need for controlled substance registrations, these forms play a critical role in regulating activities that could pose risks to community health or safety, emphasizing compliance with state and federal laws.

Dos and Don'ts

Filling out the New Jersey Dangerous Substance Registration form is a pivotal step for healthcare professionals who manage, dispense, or prescribe controlled substances within the state. To help ensure the process is done correctly and to avoid common pitfalls, here are several dos and don'ts to consider:

  • Do read the entire instruction sheet provided before beginning your application. This will give you a clear understanding of the requirements and help you avoid any mistakes.
  • Do ensure that your check or money order for $20.00 is made payable to “State of New Jersey.” This fee is crucial for processing your application.
  • Do use a ballpoint pen for filling out the form if you're not typing it, as this ensures the information is legible and enduring on the form.
  • Do include a current, physical New Jersey location where the controlled dangerous substances will be handled, not just a P.O. Box.
  • Do ensure that your New Jersey professional license number is current and active, writing it in “Section B” of the application without errors.
  • Don't forget to check if additional space is needed for your responses. If so, attach a separate sheet of paper, clearly identifying the related section(s) of the application.
  • Don't neglect to disclose any past restrictions, arrests, or convictions related to controlled substances, as failing to do so can have serious implications for your application.
  • Don't submit the application without verifying all the information for accuracy. Double-check your answers and ensure that no required fields have been missed.
  • Don't hesitate to contact the Drug Control Unit at (973) 504-6351 if you have any questions or need further assistance. It's better to seek clarification than to submit an incorrect or incomplete form.

Misconceptions

The process of registering for a Controlled Dangerous Substance (CDS) permit in New Jersey is governed by specific regulatory requirements aimed at ensuring the safe handling of these substances. However, misunderstandings about the registration process can lead to confusion. Here are seven common misconceptions about the New Jersey Dangerous Substance Registration form, clarified to provide accurate guidance.

  • Misconception 1: Only Medical Doctors Need to Register

    This is inaccurate. The requirement for registration encompasses a broad range of professionals beyond medical doctors. Dentists, veterinarians, podiatrists, optometrists, physician assistants, advanced practice nurses, and certified nurse midwives are all required to apply if they prescribe, dispense, or handle controlled dangerous substances in New Jersey.

  • Misconception 2: A New Jersey CDS Registration Serves as a National Certification

    A New Jersey CDS registration is valid only within the state. Practitioners who wish to handle controlled substances in states outside of New Jersey must adhere to the specific registration requirements of those states. Each state has its own regulations and registration process for controlled dangerous substances.

  • Misconception 3: The Registration Process is Instantaneous

    Many assume the process is immediate. However, it typically takes between 4 to 6 weeks to process a CDS application in New Jersey. This timeframe allows the Drug Control Unit to thoroughly review applications to ensure compliance with state regulations.

  • Misconception 4: DEA Registration is Sufficient for Practicing in New Jersey

    Holding an active DEA number is not enough to legally prescribe, dispense, or conduct research with controlled dangerous substances in New Jersey. Practitioners must also secure a separate New Jersey CDS registration, highlighting the requirement for dual registration at both federal and state levels.

  • Misconception 5: Only Physicians and Pharmacies Need to Provide Their License Numbers

    Contrary to this belief, all applicants, including individual practitioners and mid-level prescribers, must include their New Jersey professional license number on the application. This ensures that every individual or firm handling controlled substances is properly licensed and registered.

  • Misconception 6: The Registration Fee is Variable

    The application instructs to include a $20.00 check or money order, payable to the State of New Jersey. This amount is a fixed fee for the registration process, contrary to the misconception that fees vary based on the type or quantity of controlled substances handled.

  • Misconception 7: Any Address Can Be Provided on the Registration Form

    The regulations specify that the address provided must be an actual physical location where the controlled substances will be stored, prescribed, dispensed, etc. A P.O. box is not acceptable for this purpose, underscoring the importance of providing a verifiable location for the safe handling of these substances.

Understanding these nuances is crucial for compliant and effective management of controlled substances within New Jersey. By dispelling these misconceptions, professionals can better navigate the registration process and uphold the state's commitment to public health and safety.

Key takeaways

Filling out the New Jersey Dangerous Substance Registration form is crucial for practitioners and businesses managing controlled dangerous substances. Here's what you need to know:

  • Registration with the New Jersey Office of the Attorney General, Division of Consumer Affairs, Drug Control Unit is mandatory for anyone manufacturing, prescribing, distributing, dispensing, or conducting research with controlled substances in New Jersey.
  • The form applies to a broad range of professionals including medical doctors, dentists, veterinarians, and pharmacies, each with specific requirements.
  • A $20.00 fee, payable to the "State of New Jersey," must accompany your application. The processing time for applications is typically 4-6 weeks.
  • Your New Jersey C.D.S. registration will only be valid for the New Jersey location specified in your application, and it's important to provide a physical address, not just a P.O. Box.
  • If you're moving your practice to New Jersey and already have a D.E.A. number, you can request to transfer it by providing the necessary documentation to the Drug Enforcement Administration.
  • Practitioners who plan to operate in New Jersey and another state must obtain a separate D.E.A. registration for each location.
  • Applicants must have an active and current New Jersey professional license number, which needs to be included in the application.
  • Limits on what can be prescribed or dispensed vary by practitioner type, with specific rules for advanced practice nurses and optometrists regarding controlled substances.
  • Ensure all sections of the application are fully completed, and if more space is needed for any question, attach a separate sheet indicating the section(s) responded to.

By carefully following these guidelines, healthcare providers and businesses can ensure compliant practice in the handling and management of controlled substances within New Jersey.

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