MODIFICATION
B -- Centralized Chemopreventive Agent Repository and Chemistry Support
- Notice Date
- 12/8/2010
- Notice Type
- Modification/Amendment
- NAICS
- 541690
— Other Scientific and Technical Consulting Services
- Contracting Office
- Department of Health and Human Services, National Institutes of Health, National Cancer Institute, Bldg 1050, Frederick, Maryland, 21702, United States
- ZIP Code
- 21702
- Solicitation Number
- SS-PCPSB-5003-44
- Point of Contact
- Rukshani Fernnado, Phone: 3014353783, Virginia DeSeau, Phone: 301-435-3978
- E-Mail Address
-
rf212s@nih.gov, vd9t@nih.gov
(rf212s@nih.gov, vd9t@nih.gov)
- Small Business Set-Aside
- N/A
- Description
- This is an amendment to provide clarification and to extend the due date to December 20, 2010 by 3:00pm. The following additional information is provided as a result of questions asked: Technical Approach b. Demonstration of an understanding of preclinical and clinical study support needs 1.Can you please clarify NIH's intent with this experience/expertise requirement? This information will be addressed in the RFP. c. Experience in delivery of biological materials and laboratory services 2. What are the analytical instrumentation and services being requested? Research materials will have specifications with analytical testing required for stability testing, periodic testing, acceptance testing and release testing. Typical instrumentation required for pharmaceutical analysis includes UV-VIS, HPLC, IR, GC, dissolution apparatus and other specialty testing as needed. This testing may be obtained through subcontracted analytical services. 3. Are you requesting the service provider to acquire the clinical material or are you requesting the experience in the receipt process of biological materials? The service provider will be required to obtain research materials through a variety of mechanisms including custom synthesis and biotech processes. Facilities d. Separate office, preclinical, clinical, laboratory, quarantine, storage and shipping/receiving areas 1. Is the service provider required to have a preclinical and a clinical facility or the ability to store preclinical and clinical material and to provide such material to a preclinical and clinical facility? The pre-clinical and clinical materials must be stored separately although they may be housed in the same facility.
- Web Link
-
FBO.gov Permalink
(https://www.fbo.gov/spg/HHS/NIH/FCRF/SS-PCPSB-5003-44/listing.html)
- Record
- SN02340363-W 20101210/101208233926-1d1098a2fb832213a25460901b11cd16 (fbodaily.com)
- Source
-
FedBizOpps Link to This Notice
(may not be valid after Archive Date)
| FSG Index | This Issue's Index | Today's FBO Daily Index Page |