Dept.
of
Health
and
Human
Services,
Health
Resources
and
Services
Administration,
Healthcare
Systems
Bureau OMB
No.
0915-0327;
Expiration
Date:
XX/XX/20XX
INSTRUCTIONS FOR COMPLETING THE 340B REGISTRATION FORM
For use by any site registering as a Sexually Transmitted Disease Clinic. Specific eligibility requirements are posted on the OPA website.
An organization eligible to participate in the 340B Program must complete the registration process in order to purchase and use 340B drugs for its eligible patients. This registration must be completed and submitted according to the established deadlines that are published on the OPA website. The registration process is not complete unless all necessary supporting documentation is submitted on the same day to OPA. Once the Office of Pharmacy Affairs (OPA) receives an entity’s registration and verifies that the organization is eligible, the entity may purchase 340B drugs beginning on the entity’s participating start date listed on the 340B database.
The entity should ensure that all information is current and accurate on the 340B database record. It is the covered entity’s responsibility to notify OPA of any changes by submitting an official 340B Program change request.
NOTE ON SHIPPING ADDRESSES – complete this section ONLY if your covered entity’s 340B drugs will be shipped to an address that is different from the covered entity address. Covered entities should be aware that listing a location as a shipping address does not make that location eligible to use 340B drugs for any individuals treated there. However, do NOT use this section to provide information for a contract pharmacy arrangement. Please refer to the OPA website for instructions on registering a contract pharmacy.
Once your registration has been processed, OPA will notify you (at the e-mail address that you provide) of your covered entity’s 340B Program participation start date and provide you with your 340B identification number, a unique number that OPA assigns to each covered entity. Please use this number in all correspondence to OPA. 340B identification numbers will be used by manufacturers, wholesalers, and others to search the OPA database to verify your participation in the 340B Program. It is the entity's responsibility to notify its wholesaler or manufacturer that it is registered for 340B prices when it places an order.
This registration form must be completed and submitted according to the established deadlines that are published on the OPA website (www.hrsa.gov/opa).
Public Burden Statement: An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. The OMB control number for this project is 0915-0327. Public reporting burden for this collection of information is estimated to average 1.0 hour per response, including the time for reviewing instructions, searching existing data sources, and completing and reviewing the collection of information. Send comments regarding this burden estimate or any other aspect of this collection of information, including suggestions for reducing this burden, to HRSA Reports Clearance Officer, 5600 Fishers Lane, Room 10C-03I, Rockville, Maryland, 20857.
.
340B PROGRAM REGISTRATION FORM FOR SEXUALLY TRANSMITTED DISEASE CLINICS
Acknowledgement of Covered Entity Participation in Outpatient Discount Drug Pricing under Section 340B of the Public Health Service Act.
Covered Entity Name:
Covered Entity Sub-Division Name (if applicable):
Employer Identification Number:
Street Address (PO Boxes are not allowed):
City: _ State: ZIP:
City: _ State: ZIP:
Shipping Address (if different; PO Boxes are not allowed)
City: _ State: ZIP:
Are you attempting to reinstate under a previous 340B ID number?
Yes 340B ID Number: ________________________
No
UDS or Grant Number (if known):
Nature of Support:
Direct Funding (dollars received from CDC or an intermediate organization)
“In-kind” products or services purchased with Section 318 funds
None
Note: In-kind contributions may be in the form of real property, equipment, supplies and other expendable property, and goods and services directly benefiting and specifically identifiable to the project or program.
Will the covered entity dispense 340B purchased drugs to Medicaid patients AND subsequently bill Medicaid for those dispensed 340B drugs? Yes No
If “Yes”, please provide the entity’s Medicaid Provider Number(s) (MPN) and/or National Provider Identifier(s) (NPI) for each applicable entity location that bills Medicaid for 340B drugs. If you are unsure of the entity’s MPN and/or NPI, please check with your State Medicaid agency. It is important that your Medicaid billing status and appropriate provider identifier number(s) are accurate in the OPA database and align with your billing practices in order to prevent Medicaid rebates on drugs that were purchased at the 340B discounted price.
Medicaid Provider Number(s) and/or _
National Provider Identifier(s) and/or
All covered entities should notify OPA prior to any change in Medicaid billing status. For more information, please visit the HRSA website.
Covered Entity Primary Contact Name
(Must be someone employed by the Covered Entity):
Title:
Phone: Ext. _ Fax:
Email Address:
Covered Entity Authorizing Official
The Authorizing Official must be someone who can bind the organization into a contract, such as the President, Vice President, Chief Executive Officer, Chief Operating Officer, Chief Financial Officer, or Executive Director. Forms that are signed by an individual that OPA determines is not an acceptable representative will not be processed. If you are in doubt regarding the acceptability of a signature, please contact please contact the 340B Prime Vendor Program at 1-888-340-2787 or via email at [email protected] prior to submission of your registration.
Authorizing Official Name:
Title:
Phone: Ext. _ Fax:
Email Address:
The undersigned represents and confirms that he/she is fully authorized to legally bind the covered entity and certifies that the contents of any statement made or reflected in this document are truthful and accurate. The undersigned further acknowledges the 340B covered entity’s responsibility to abide by the following:
As an Authorized Official, I certify on behalf of the covered entity that:
all information listed on the 340B Program database for the covered entity will be complete, accurate, and correct;
the covered entity will meet all 340B Program eligibility requirements;
the covered entity will comply with all requirements of Section 340B of the Public Health Service Act and any accompanying regulations including, but not limited to, the prohibition against duplicate discounts and diversion (section 340B(a)(5)(A) and (B) of the Public Health Service Act;
the covered entity will maintain auditable records pertaining to compliance with the requirements described in paragraph (3) above, pursuant to section 340B(a)(5)(C) of the Public Health Service Act;
if the covered entity uses contract pharmacy services, that the contract pharmacy arrangement will be performed in accordance with OPA requirements and guidelines;
the covered entity acknowledges its responsibility to contact OPA as soon as possible if there is any change in 340B eligibility and/or breach by the covered entity of any of the foregoing; and
the covered entity acknowledges that if there is a breach of the requirements described in paragraph (3) that the covered entity may be liable to the manufacturer of the covered outpatient drug that is the subject of the violation, and, depending upon the circumstances, may be subject to removal from the list of eligible 340B entities.
In addition, I have read all applicable registration instructions and I am aware that my registration will not be reviewed if the required supporting documents are not submitted today.
Please provide any additional information or clarification that may be helpful in reviewing this registration for 340B program eligibility: _________________________________________________________________________________________
_________________________________________________________________________________________________
_________________________________________________________________________________________________
Signature of Authorizing Official: Date:
_
File Type | application/vnd.openxmlformats-officedocument.wordprocessingml.document |
File Title | PHARMACY AFFAIRS BRANCH |
Author | SCHEN |
File Modified | 0000-00-00 |
File Created | 2021-01-25 |