A19. Attachment 02 ADR Agreement.docx
DOCX document 23 KB Posted
- Attached to
- FY26 Pediatric FLU Federal contract opportunity
- Solicitation number
- 75D30125R73357
About this file
This document is an Authorized Distributor of Record (ADR) Agreement between the Centers for Disease Control and Prevention (CDC) and a manufacturer/supplier of pediatric vaccines. The agreement establishes CDC's status as an authorized distributor under the Prescription Drug Marketing Act (PDMA) of 1988, specifically for the Vaccine for Children (VFC) program, which provides vaccines to eligible children including Medicaid-eligible, uninsured, American Indian/Alaska Native, and children with limited health insurance coverage.
The agreement allows CDC to distribute specific vaccines, with provisions for either full product line distribution or a limited list of products (to be specified in Attachment A-1). The agreement is valid until terminated by either party with 90 days written notice and does not constitute a sales agreement, but rather defines an ongoing distribution relationship. The related federal contract opportunity (Solicitation Number 75D30125R73357) is for FY26 Pediatric FLU vaccines, targeting manufacturers of pediatric vaccines who can supply vaccines through the VFC program and potentially utilize both VFC and Section 317 vaccine purchase funds.
View the file
Other files for this federal contract opportunity
| File | Type | Posted |
|---|---|---|
| 75D30125R73357 0001 Ped FLU.docx | DOCX document | |
| A19. 75D30125R73357 0001.pdf | ||
| A19. Attachment 03 List of Products.docx | DOCX document | |
| A19. 75D30125R73357.pdf | ||
| A19. Attachment 01 List of Vaccines.docx | DOCX document |
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Text version
Attachment 2: Authorized Distributor of Record (ADR) Agreement
AUTHORIZED DISTRIBUTOR OF RECORD (ADR) AGREEMENT
This Agreement hereby represents the ongoing relationship between the supplier named below (“MANUFACTURER / SUPPLIER”) and the Centers for Disease Control and Prevention, herein after referred to as CDC, to establish and designate CDC as an Authorized Distributor of Record (ADR) as set forth in the Prescription Drug Marketing Act (PDMA) of 1988 as well as in the implementing federal regulations found at 21 CFR Part 203. CDC hereafter agrees to comply with all applicable state and federal laws to ensure continued status of this relationship. To further meet the requirements of the PDMA, please forward with the signed agreement an attachment with a list of the specific products that CDC is authorized to distribute or a statement that the CDC is an ADR for the manufacturer’s entire product line. Specific products should be identified by the pharmaceutical / vaccine name, dosage form, and strength of the drug and the NDC number.
Check the box that applies:
__ The Distributor is the ADR for Supplier’s entire product line.
__ The Distributor is the ADR for the products listed on the attachment A-1.
This agreement shall be valid from the date of dual execution until termination by either party on ninety (90) days written notice. This agreement shall not abridge, supplant, modify, or in any way alter any other pre-existing distribution agreement or any future agreements that may, from time to time, be executed in the furtherance of the business relationship between Manufacturer/ Supplier and the CDC.
This agreement confers no rights upon CDC other than to designate CDC as an Authorized Distributor of Record for Manufacturer / Supplier. This agreement is not intended to be, nor shall it be, interpreted as a sales agreement or any other type of agreement other than to represent an “ongoing relationship” within the meaning set forth in 21 CFR Part 203.3(u).
By affixing my signature below, I do hereby acknowledge and represent that I have read this Agreement in its entirety, that I understand its terms, that I am duly authorized to bind my organization to the requirements detailed in the above Agreement and that I agree to ensure that my organization will adhere to such requirement for the duration herein stated.
Authorized Distributor of Record: Centers for Disease Control and Prevention (CDC)
Authorized Signature:________________________________________
Print Name: , U.S. Government Contracting Officer
Date: _________________
Manufacturer / Supplier: _____________________________
Authorized Signature: ________________________________
Print Name: ________________________________________
Date: ______________
ATTACHMENT A-1
LIST OF PRODUCTS
| Item No. |
| Product/Brand Name |
| NDC |
| 1. |
| Vaccine |
| xxxxx-xxxx-xx |
| 2. |
| Vaccine |
| xxxxx-xxxx-xx |
| 3. |
| Vaccine |
| xxxxx-xxxx-xx |
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