Sources Sought Vendor Feedback Questions-CDER-2025-128753.pdf
PDF 134 KB Posted
- Solicitation number
- CDER-OTS-25-C-1691
About this file
This document is a Sources Sought Vendor Feedback Form for a potential federal contract opportunity with the FDA's Office of Clinical Pharmacology (OCP)/Division of Applied Regulatory Science (DARS). The form is designed to gather market research information from potential vendors about high-pressure liquid chromatography (HPLC) core-shell technology columns and consumables. Key questions address vendor capabilities, small business status, manufacturing origin, service provision, and existing federal contract vehicles.
The form targets vendors in NAICS code 541715 (Research and Development in Physical, Engineering, and Life Sciences) and seeks detailed feedback about their ability to provide laboratory supplies. Vendors are invited to complete the form, provide capability statements, and offer comments on draft Statement of Work requirements. The document explicitly states this is a market research effort and not a commitment to issue a solicitation or award a contract. Socioeconomic status options include small business, 8(a)/ANC, HUBZone, service-disabled veteran-owned, women-owned small, and EDWOSB categories.
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Other files
| File | Type | Posted |
|---|---|---|
| Sources Sought Notice- FDA Office of Clinical Pharmacology (OCP)_Division of Applied Regulatory Science.doc | DOC document | |
| Draft Statement of Work-CDER-2025-128753.docx | DOCX document |
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Vendor Feedback Form
Vendor/Company Name:
Vendor/Company DUNS:
Vendor/Company POC:
Socioeconomic Status: (Check all that apply)
Small Business 8(a)/ANC HUBZone Service-Disabled Veteran-Owned Women-Owned Small EDWOSB
Suggested NAICS Code (The FDA is considering 541715 - Research and Development in the Physical, Engineering, and Life Sciences):
1. Is your company considered small under the NAICS code 541715?
2. Is your company the manufacturer or distributor? What is the manufacturing country of origin of these items?
3. If your company is a small business and your company is an authorized distributor/reseller for the items identified above (or equivalent product/solutions), does your company alter or modify the items requested in any way? If so, please explain how the items are modified or altered.
4. Does your company provide all the services in the draft SOW?
YES NO
a. Do you provide these services under any existing Federal contract vehicle(s) (e.g., GSA schedules, Government-wide acquisition contracts (GWACs), agency-specific acquisition contracts or IDIQs) that the FDA may utilize the existing contract for the requested services?
YES NO
If Yes is selected, please list any available contract vehicle number(s), the current Contract End Date, the Contract End Date including all unexercised options, and ordering instructions.
5. Please provide any additional comments, concerns or feedback regarding the draft SOW requirements.
Track changes and comments in the draft SOW MS Word document are encouraged.
6. Interested vendors may also provide any capability statements/information sheets in their response.
This SSN is not to be construed as a commitment by the Government to issue a solicitation or ultimately award a contract. Any information provided in response to this RFI is to be used for market research purposed only.
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