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Navigating the complexities of managing, prescribing, or distributing controlled dangerous substances in New Jersey requires adherence to strict regulatory procedures, as outlined in the New Jersey Application Registration form. This form, a gateway to compliance under the New Jersey Controlled Dangerous Substances Act, N.J.S.A. 24:21-1 et seq., serves a critical function for professionals and firms operating within the state. Eligibility extends to a broad array of healthcare and research professionals, including but not limited to, physicians, dentists, veterinarians, and pharmacies, each mandated to secure registration for legitimizing their dealings with such substances. Key stipulations include a mandatory fee, specifics about registrants, and the necessity for both state and federal registration, minus an exemption for federal facilities. Additionally, this process entails a check for past legal or regulatory issues related to controlled substances, ensuring that applicants meet a standard of integrity expected in the handling of these materials. With a processing timeline of 4-6 weeks and the need for accompanying documentation such as a professional license and, if applicable, details for transferring an existing D.E.A. number to New Jersey, applicants are advised to meticulously prepare their submissions to expedite approval and avoid common pitfalls. The form not only underscores New Jersey’s stringent oversight in controlling the distribution and use of potentially dangerous substances but also delineates the responsibilities and qualifications required of applicants to foster a compliant and safe environment for both practitioners and the public.

Sample - Nj Application Registration Form

New Jersey Office of the Attorney General

Division of Consumer Affairs

Drug Control Unit

124 Halsey Street, 6th 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 firm 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 $40.00 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 file 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 verification letter from the licensing board;

b.a copy of your New Jersey C.D.S. registration or a verification 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 certificate.

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 certified nurse midwives. Pharmacies must complete a separate application.

b.Every person or firm 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 office 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.

Rev. 3/19

New Jersey Office 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 clearly.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

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

Pharmacy permit number _____________________________________

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

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

 

pharmacy/facility location.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

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

________________________________________________________

 

administrative or managerial responsibility for the registered location.

 

 

 

Pharmacy permit trade name

 

 

 

 

 

 

 

 

 

 

 

 

 

________________________________________________________

 

 

 

 

Last name

 

 

 

 

First name

 

 

 

 

 

 

 

 

MI

 

 

 

 

 

 

C.D.S. – Responsible Individual

 

 

 

 

 

 

 

 

 

 

 

 

 

________________________________________________________

 

 

 

 

 

Department

 

 

 

 

 

 

 

 

Room number

 

 

 

 

 

________________________________________________________

 

 

 

 

 

 

 

 

Street address

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

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

________________________

New Jersey

__________________

 

 

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

 

City

 

 

 

 

 

 

 

 

 

ZIP code

 

 

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

____________________________

__________________________

 

 

 

 

 

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 ($40)

 

 

 

 

 

 

 

 

 

 

 

 

 

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

 

 

 

 

 

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

 

 

 

 

 

Schedule

 

 

II

 

III

 

 

IV

 

 

 

 

 

V

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Section D: Certification

 

 

 

 

 

 

 

 

 

 

 

 

 

 

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

 

 

 

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

 

 

 

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

I, _____________________________________ being duly sworn, depose

the District of Columbia or in any other jurisdiction?*

 

 

 

 

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

 

 

 

 

 

 

 

 

 

 

 

 

 

Yes

 

 

No

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

identified intis application; that the information given in this application and

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

all submitted materials contain no willful misrepresentations and that the

connection with controlled substances under federal law or the laws

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

information is true and complete. I understand that should an investigation

jurisdiction?*

 

 

 

 

 

 

 

 

Yes

No

at any time disclose otherwise, my application may be rejected, and I may

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

face legal sanctions if I am already registered. I understand that in signing

controlled drug registration revoked, suspended or denied in New

this application for registration, I am consenting to any reasonable inquiry

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

that may be necessary to verity the information that I have provided on this

jurisdiction?*

 

 

 

 

 

 

 

 

Yes

No

form or may provide in conjunction with this application.

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

 

 

 

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

 

 

 

or employee who has access to controlled dangerous substances been

 

 

 

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

 

Applicant's signature

 

 

 

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

 

 

 

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

 

Date

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.

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.

DDC-25 Revised 3/19

Document Specifications

Fact Detail
Application Purpose Required for individuals or firms involved in the manufacture, prescription, distribution, dispensation, research, or analysis of controlled dangerous substances in New Jersey.
Governing Law New Jersey Controlled Dangerous Substances Act, N.J.S.A. 24:21-1 et seq.
Location Specificity Registration is only valid for the specific New Jersey location provided in the application.
Application Fee A fee of $40.00 is required with the submission, payable to “State of New Jersey.”
Processing Time The application process takes approximately 4-6 weeks.
DEA Number Transfer If already holding a current DEA number in another state and discontinuing practice there, it can be transferred to New Jersey with proper documentation.

Detailed Steps for Using Nj Application Registration

Filling out the NJ Application for Registration for controlled dangerous substances involves a detailed process to ensure you meet New Jersey's legal requirements. This application is necessary for professionals and entities that handle controlled substances within the state, including physicians, dentists, pharmacies, and research institutions. Completing this form accurately is crucial for compliance with state laws and for the smooth operation of your practice or business. Here's a step-by-step guide to help you navigate through the form:

  1. Start with Section A: Fill in all required items, which include providing the name of the applicant and the business or professional address in New Jersey. Remember, a P.O. box is not acceptable as the sole address.
  2. In Section B, titled "Pharmacy Licensure Information," if applicable, provide your pharmacy permit number and ensure it aligns with the New Jersey location for which you're registering.
  3. Proceed to Section C, "Business Information":
    • Enter the name, address, and telephone number of the individual responsible for the registered location.
    • List the name, address, and telephone number of the registered agent if the applicant is a corporation, or the name and address of a New Jersey resident who can accept legal documents on behalf of a nonresident proprietor or partner.
  4. In Section D, check the relevant boxes to indicate the type of dispenser you are and the schedules of controlled dangerous substances for which you are applying. Attach the $40.00 fee payable to "State of New Jersey."
  5. Answer all eligibility and background questions in Section D truthfully, including any past restrictions, arrests, or convictions related to controlled substances, and whether you’ve ever had a registration surrendered, revoked, suspended, or denied.
  6. If any section requires additional space for your responses or you need to provide explanations for “Yes” answers to any background questions, attach a separate sheet of paper clearly indicating the sections and questions your additional information relates to.
  7. Sign and date the form in Section D under the Certification area, affirming that all the information provided is true and complete, and acknowledging your consent to any necessary inquiries to verify the information.
  8. Review the form to ensure all sections are completed and no required information is missing. Attach your $40.00 fee, any additional explanatory sheets, and requested documentation.
  9. Mail the completed application, along with the necessary fee and documents, to the address provided at the top of the form: New Jersey Office of the Attorney General Division of Consumer Affairs Drug Control Unit, 124 Halsey Street, 6th Floor, P.O. Box 45045, Newark, NJ 07101.

After submission, the processing of your application will take about 4-6 weeks. Once approved, your New Jersey Controlled Dangerous Substance registration will be sent to the mailing address on file with your professional licensing board. It’s important to ensure that all information remains up to date during this period to avoid any delays in receiving your registration.

Learn More on Nj Application Registration

What is the purpose of the New Jersey Controlled Dangerous Substance (C.D.S.) registration?

The New Jersey Controlled Dangerous Substance (C.D.S.) registration is required for individuals and firms involved in the manufacture, prescription, distribution, dispensing, or research of controlled dangerous substances within the state. This requirement, as outlined under N.J.S.A. 24:21-1 et seq., ensures that activities involving these substances are monitored and conducted within legal and regulatory frameworks to prevent misuse and diversion.

Who needs to obtain a C.D.S. registration in New Jersey?

A wide range of professionals and entities must obtain a C.D.S. registration in New Jersey. These include but are not limited to:

  • Medical doctors, dentists, optometrists, veterinarians, and podiatrists
  • Mid-level practitioners like physician assistants, advanced practice nurses, and certified nurse midwives
  • Firms and individuals engaged in the manufacture, distribution, or dispensing of controlled dangerous substances
  • Entities conducting research or analysis using controlled dangerous substances
  • Pharmacies, which are required to submit a separate application

It's important to note that both state and federal registrations are necessary for handling controlled dangerous substances in New Jersey.

What is the process for transferring a D.E.A. number to New Jersey?

Professionals who have a current D.E.A. number in another state and wish to practice in New Jersey need to transfer their D.E.A. number by submitting:

  1. A copy of their New Jersey professional license or a verification letter from the licensing board
  2. A copy of their New Jersey C.D.S. registration or a verification letter
  3. A copy of their out-of-state D.E.A. registration
  4. A letter requesting an address change to match the New Jersey C.D.S. registration

All documentation must be provided to the Drug Enforcement Administration at their Newark office. This step is crucial for ensuring the D.E.A. number is valid in New Jersey.

What should I do if I need more space to respond to questions on the application?

If the space provided on the application is insufficient for your responses:

  • Submit a separate sheet of paper
  • Clearly identify the section(s) of the application your responses correspond to

This additional documentation should be included with your application package to ensure a comprehensive review of your qualifications for the C.D.S. registration.

Common mistakes

  1. Failing to provide an actual physical address where controlled substances are managed, mistake often made due to misunderstanding of the instructions requiring a physical location, not just a P.O. Box. This requirement ensures that the site of substance management can be properly inspected and regulated, according to state law.

  2. Using professional or corporate names instead of the individual practitioner's name or the pharmacy's trading name when filling out the application. Individuals, such as medical doctors and dentists, are instructed to use their own names, while pharmacies should use their common trading names, which can lead to confusion if not carefully observed.

  3. Omitting the current and active New Jersey professional license number in the specified section of the form. This oversight can occur when applicants overlook the specific directive to include this crucial piece of information that verifies their legal capacity to dispense or prescribe controlled dangerous substances within New Jersey.

  4. Not correctly selecting the schedules of controlled dangerous substances they are applying for, due to a misunderstanding of the federal classification system or the specific substances they are authorized to handle. This mistake directly impacts the scope of their legal operations regarding controlled substances.

  5. Ignoring the requirement to attach additional documentation when transferring a D.E.A. number to New Jersey or when any of the application questions related to criminal history or previous registration issues are answered affirmatively. This documentation is critical for providing context and verifying the applicant’s eligibility for registration.

  6. Insufficiently detailing the roles of individuals with managerial or administrative responsibilities at the registered location or failing to accurately list the contact information of a registered agent or New Jersey resident for process serving, as required for corporations or nonresident proprietors. This involves overlooking the need to clearly articulate the oversight structure for controlled substances at the location.

Common errors such as these underscore the importance of attentively reviewing the New Jersey Controlled Dangerous Substances application instructions and accurately completing every section to comply fully with state regulations. Mistakes in the application process not only delay the issuance of a C.D.S. registration but may also result in legal complications for the applicant, emphasizing the need for thoroughness and precision.

Documents used along the form

When applying for a Controlled Dangerous Substance (C.D.S.) registration in New Jersey, the complexity of managing controlled dangerous substances requires thorough documentation and adherence to both state and federal guidelines. Below is a list of additional forms and documents often needed alongside the NJ Application Registration form. Each of these plays a vital role in ensuring compliance and facilitating the registration process.

  • Copy of New Jersey Professional License or Verification Letter: An applicant must provide a copy of their current New Jersey professional license or a verification letter from the New Jersey licensing board. This confirms the applicant’s legal standing to practice in their profession within New Jersey.
  • Copy of Out-of-State D.E.A. Registration (if applicable): If the applicant holds a D.E.A. registration in another state that they plan to transfer to New Jersey, a copy of this registration is required. This is necessary when an applicant wishes to change their practice location to New Jersey but maintain their federal registration.
  • Letter Requesting Address Change (if applicable): A letter requesting an address change is necessary when transferring a D.E.A. registration from another state. This letter should match the New Jersey address listed on the C.D.S. registration application.
  • D.E.A. Registration Application for New Jersey: For those who intend to practice in New Jersey and another state, a separate D.E.A. registration for New Jersey is required. This application ensures that the practitioner is compliant with federal regulations within New Jersey.
  • Proof of Secure Storage Facilities: While not explicitly listed in the enclosed instruction sheet, applicants must ensure they have secure storage solutions for controlled substances. Proof of these facilities, while not always required at the time of application, may be necessary upon inspection or request.
  • Background Check Documentation: Given the sensitive nature of controlled substances, a background check may be required. This documentation helps confirm the applicant’s suitability by revealing any past criminal activities related to controlled substances.

Each document serves its unique purpose, from verifying professional eligibility to ensuring the secure and responsible handling of controlled substances. Collectively, they contribute to a comprehensive vetting process, safeguarding public health and welfare. Proper preparation and submission of these documents, along with the C.D.S. application, streamline the registration process, helping applicants to navigate legal requirements with greater ease.

Similar forms

The New Jersey Controlled Dangerous Substances (CDS) application form bears similarity to the Federal Drug Enforcement Administration (DEA) Registration Application for a variety of reasons. Both forms are designated for entities or individuals involved in the handling of controlled substances, such as prescribing, manufacturing, or dispensing. They require detailed information about the applicant's licensing and location of practice. Additionally, both forms necessitate disclosing any past criminal activities or disciplinary actions related to controlled substances, ensuring that applicants meet specific legal and professional standards to be granted the privilege to work with these substances.

Another document similar to the New Jersey CDS application is the Pharmacy Permit Application that many states require. This form is specifically designed for pharmacies that need authorization to operate within a state. Like the CDS application, the Pharmacy Permit Application asks for detailed business information, proof of compliance with state regulations, and the qualifications of staff members. Both applications serve as critical gateways to ensuring that entities distributing medications or controlled substances maintain high standards of practice and compliance with state laws.

The Healthcare Professional Licensing Application, which healthcare providers must complete to practice in a given state, shares similarities with the New Jersey CDS registration form. Both require detailed professional information, including licensure status and disciplinary history. These forms work together to regulate access to practicing within medical and related health fields, especially in roles involving controlled substances, to ensure that only qualified and legally compliant individuals are granted the privilege.

The New Jersey Alcoholic Beverage Control (ABC) Licensing Application, though focused on a different sector, also parallels the CDS application in structural ways. Each requires the applicant to provide detailed personal or business information, address history of regulatory compliance, and if applicable, criminal history, underscoring the importance of regulatory oversight in sensitive business operations. The correlation highlights how various regulatory frameworks operate similarly to safeguard public health, safety, and welfare.

The Employment Eligibility Verification Form (I-9) shares a procedural similarity with the CDS application, despite serving different purposes. Both forms are necessary for verification processes; the I-9 verifies an individual's eligibility to work in the United States, while the CDS application verifies an applicant's eligibility to handle controlled substances. They both require the provision of personal and professional details to meet regulatory standards.

State-level Environmental Permit Applications, necessary for businesses that could impact the environment, share a common foundation with the CDS application in terms of regulatory compliance. Both types of applications are centered around ensuring applicants adhere to specific state regulations and standards to operate legally within the state. This similarity highlights the broader concept of how various forms of state regulation manage different facets of public health and safety, from environmental protection to drug control.

The Business Licensing Application, which entrepreneurs must complete to legally operate a business within many states, shares several commonalities with the CDS application. Both require detailed information about the business or practice, including ownership structure and operational details. These applications ensure entities are properly registered with state authorities and meet all regulatory requirements to conduct their respective activities.

Lastly, the Professional Liability Insurance Application for healthcare providers mirrors the New Jersey CDS application in certain aspects. While focusing on liability coverage, it similarly requires extensive professional information, including licensure and any history of disciplinary actions, to assess risk and eligibility. The parallel between managing professional liability and controlling substance handling underscores the layered precautions in place to maintain standards within healthcare professions.

Dos and Don'ts

When it comes to navigating the intricacies of the New Jersey Application Registration form for Controlled Dangerous Substances (C.D.S.), there are several key approaches to ensure the process is as smooth as possible. Here's a concise guide on the do's and don'ts:

  • Do ensure that the information provided on the application is accurate and up-to-date. Double-check all entries, especially your New Jersey professional license number and personal details.
  • Do make sure that the address you provide is the actual location where controlled dangerous substances will be stored, prescribed, or dispensed. Remember, P.O. boxes are not acceptable for this purpose.
  • Do pay close attention to the specific requirements for your profession under section 3.a of the instruction sheet. Whether you're a medical doctor, dentist, or veterinarian, among others, understanding the unique stipulations for your field is crucial.
  • Do include the required $40.00 fee with your application, making the check or money order payable to "State of New Jersey". Missing or incorrect payment can delay processing.
  • Do provide additional sheets of paper if more space is needed to adequately respond to any question on the application. Clearly identify the sections your responses correspond to.
  • Do sign the certification section, understanding that this signifies your consent to any reasonable inquiry necessary to verify the information you've provided.
  • Don't overlook the need for both a state and federal registration if you're handling controlled dangerous substances. Each registration plays a critical role in compliance.
  • Don't use a professional association, corporation, or partnership name in place of your individual practitioner name if you're applying as an individual practitioner.
  • Don't forget to check the specific registration requirements if you hold a D.E.A. number in another state but plan to practice in New Jersey. The implications of transferring or obtaining a new registration are important.
  • Don't ignore the question regarding any restrictions, arrests, convictions, or disciplinary actions related to controlled substances. Being transparent is essential, and additional information must be attached if you answer "Yes" to any of these questions.
  • Don't submit the application without verifying that every section is completed and all required documents are attached. Incomplete applications can lead to unnecessary delays.
  • Don't underestimate the importance of regularly checking the address on file with your professional licensing board. This address is where your C.D.S. registration will be mailed.

Adhering to these guidelines helps streamline the application process, ensuring compliance with New Jersey's regulations for controlled dangerous substances. Whether you're new to the profession or navigating the renewal process, attention to detail and thoroughness are your best tools for success.

Misconceptions

When navigating the complexities of the New Jersey Application Registration form for Controlled Dangerous Substances (C.D.S.), professionals may encounter a variety of misconceptions. Clear understanding is crucial for compliance and ensuring the lawful handling of controlled substances within the state. Below are eight common misconceptions and the facts to dispel them:

  • Only medical doctors need to register. In reality, the registration requirement extends beyond medical doctors to include dentists, veterinarians, optometrists, and even mid-level practitioners such as physician assistants and advanced practice nurses. Every individual and firm dealing with controlled substances must be registered according to state law.
  • A D.E.A. number is enough to operate across states. This assumption is incorrect. While a D.E.A. number is necessary, it is only valid in the state listed on the certificate. To legally handle controlled substances in New Jersey, professionals must obtain a separate New Jersey C.D.S. registration.
  • You can use a P.O. box for the address on the form. The form specifically requires a current, actual location where controlled substances will be handled. A P.O. box alone does not satisfy this requirement, illustrating the state's commitment to accurate and accountable record-keeping.
  • Pharmacies are not required to have a separate application. This is not the case. Pharmacies must fill out a separate application, underlining the different roles and responsibilities entities have in the controlled substance supply chain.
  • Only New Jersey locations are covered. Though it might seem restrictive, the regulation ensures a focused oversight. A New Jersey C.D.S. registration is indeed issued solely for locations within the state, emphasizing the local nature of the registration process.
  • Any professional corporation name can be used on the application. Individual practitioner applicants must use their own names rather than the names of professional associations, corporations, or partnerships. This stipulation ensures clarity regarding who bears the responsibility for controlled substances.
  • Advanced Practice Nurses can maintain stock supplies of medications. This is inaccurate. While Advanced Practice Nurses are permitted to prescribe controlled dangerous substances, they are not allowed to purchase or maintain stock supplies of those medications. This rule is designed to maintain strict control over substance distribution.
  • The registration process is immediate. Processing the application takes 4-6 weeks, a timeline that applicants should plan for to avoid disruptions in their ability to legally handle controlled substances.

Understanding these key points can alleviate concerns and ensure that professionals are well-informed about their obligations under New Jersey law. Compliance is not only about adhering to regulatory demands but also about protecting public health and safety in the handling of controlled dangerous substances.

Key takeaways

Filling out the New Jersey Application Registration form for Controlled Dangerous Substances (C.D.S.) is a critical step for professionals and entities managing these substances. Here are six key takeaways to guide you through this process:

  • Registration with the New Jersey Office of the Attorney General, Division of Consumer Affairs, Drug Control Unit, is mandatory for individuals and firms involved in manufacturing, prescribing, distributing, dispensing, or conducting research with controlled dangerous substances within New Jersey.
  • A non-refundable fee of $40.00, payable to "State of New Jersey," must accompany your application. This fee covers the cost of processing your application, which typically takes 4-6 weeks.
  • If you already have a D.E.A. number from another state and are relocating your practice to New Jersey, you can transfer your D.E.A. number to New Jersey. The transfer requires submitting specific documentation to the Drug Enforcement Administration, including a copy of your New Jersey professional license and a request for an address change.
  • The C.D.S. registration is location-specific within New Jersey. It is important to provide a current and actual address where the controlled substances will be managed. P.O. Box addresses are not acceptable.
  • Applicants must hold an active and current New Jersey professional license in the field relevant to their application. For pharmacies, the application must be completed using the pharmacy's trading name as it is known to the public, not its business or corporate name.
  • Any changes or updates to your application must be supplemented with additional sheets, clearly indicating the section(s) to which the new information pertains. This is crucial for ensuring that all your data is accurately captured and processed.

Being thorough and providing accurate information is paramount when completing the New Jersey Application Registration form for C.D.S. This will help avoid delays in the processing of your application and ensure compliance with New Jersey regulations.

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