FBO Notice Date 11/21/17
BIDS Reference Number 253
Document Type: Sources Sought
Special Studies And Analysis - Not R&D

Department of Health and Human Services, National Institutes of Health, Clinical Center/Office of Purchasing & Contracts, 20892-5480

B -- Intravenous Workflow Management and Medication Tracking System SOL NIH-CC-18-002793 DUE 120717 POC Lisa L. Schaupp, Contract Specialist, Phone 3014020735, Email Lisa.Schaupp@nih.gov
The National Institutes of Health ("NIH"), Clinical Center is conducting a market survey/sources sought notice to determine whether there is a reasonableexpectation of a responsible/capable offeror to provide an Intravenous (IV) Workflow Solution and Medication Tracking System with, at least, the characteristics listed below. Accordingly, NIH is hoping that there exists a reasonable expectation of at least two responsible/capable offerors in order for NIH to compete the requirement. Additionally, NIH is attempting to ascertain if there exists a reasonable expectation of at least two responsible/capable small business offerors in order for NIH to compete the requirement as a small business set aside.

Accordingly, NIH is seeking capability statements as to the attached SOW from other-than-small businesses, small businesses, veteran-owned small businesses,service disabled veteran-owned small businesses, HUBZONE small businesses, small businesses under the 8(a) program, and/or businesses under the GSA Schedule capable of providing a system with the following performance characteristics.

The Intravenous (IV) Workflow Solution and Medication Tracking System must be capable of providing the following.

• Provide remote verification capabilities by pharmacist of each IV medication prepared
• Provide photo verification of each dose of medication prepared
• Sorting IV medication orders into a queue for technicians to prepare based on identified priority
• Identification of errors prior to admixture
• Ability to store recipes within each product
• Ability to store lot numbers and expiration dates of each component
• HL7 integration with Allscripts to retrieve prescription information
• Quality Analytics and Reporting capabilities
• Active Directory functionality support
• Hosted server at the Clinical Center
• Medication tracking of all Intravenous (Hazardous, Non-Hazardous, Chemotherapy, and Investigational) and non-Intravenous medications prepared in the Intravenous Admixture Unit
• Ability to provide web based or mobile statusboards for pharmacy and nursing to identify medication status

THIS MARKET SURVEY/SOURCES SOUGHT ANNOUNCEMENT IS NOT A REQUEST FOR PROPOSALS, AND THE GOVERNMENT IS NOT COMMITTED TO AWARD A CONTRACT PURSUANT TO THIS ANNOUNCEMENT. CONSEQUENTLY, DO NOT SEND A PROPOSAL IN RESPONSE TO THIS NOTICE. THE APPROPRIATE RESPONSE IS A CAPABILITY STATEMENT. ALTHOUGH A RESPONDENT CAN RESPONDWITH WHATEVER INFORMATION THE RESPONDENT SEES FIT, THE IDEAL CAPABILITY STATEMENT SPECIFICALLY ADDRESSES THE REQUIREMENTS IN THE SOW AND THE REQUESTS FOR INFORMATION BELOW, AND IS NOT A GENERIC SALES BROCHURE OR MARKETING HANDOUT. FURTHER,THE GOVERNMENT REQUESTS, BUT DOES NOT MANDATE, THAT THE CAPABILITY STATEMENT ISLIMITED TO NO MORE THAN TEN PAGES. ANY PROPRIETARY INFORMATION IN THE SUBMITTEDCAPABILITY STATEMENT SHOULD BE CLEARLY MARKED AS SUCH.

The information obtained from this market research is for Government planning purposes only, and will assist the Government in planning its acquisition strategy. This is strictly market research, and the Government is not opening a question and answer period concerning this market research. Further, the Government will not pay for any costs incurred in the preparation of information in response to this market survey.

In addition to addressing the requirements listed above, the Government requests that your capability statement address the following requests for information, if relevant.

1) Please provide the full company/entity name, address including points of contact (phone number and e-mail address), DUNS numbers, and type/size of the company/entity by NAICS code.

2) If your company/entity is a dealer or service-provider, and not a manufacturer of the end items/products contemplated by the SOW, please identify your company as such and identify the end item/product manufacturers that you would be obtaining goods from in order to perform the contract, and where the manufacturers are geographically located.

3) According to the small business limitations on subcontracting standard provided by the amended Small Business Act at 15 U.S.C. § 657s, the requirement for a small business supplier is that the small business prime contractor "may not expend on subcontractors more than 50 percent of the amount, less the costof materials, paid to the concern under the contract . . . ." 15 U.S.C. § 657s(a)(2). However, "[c]ontract amounts expended by a covered small business concern on a subcontractor that is a similarly situated entity [(i.e., another small/small disadvantaged business of the same type)] shall not be considered subcontracted for purposes of determining whether the covered small business concern has violated [limitations on subcontracting.]" 15 U.S.C. § 657s(b). If you are a small business, please address your ability to adhere to limitations on subcontracting at 15 U.S.C. § 657s. To ascertain if you are a small business,use the size standard provided by NAICS Code 518210 (Data Processing, Hosting, and Related Services), with a size standard of no more than $32.5 million.

As part of this, if you are a small business that is a dealer/service-provider and not a manufacturer, please so state, and address whether you meet the following requirements from 13 C.F.R. § 121.406(b). Specifically, your company/entity:

(1) Does not exceed 500 employees (notice that the employee standard under the non-manufacturer rule is more restrictive than for NAICS Code 518210);
(2) Is primarily engaged in the retail or wholesale trade and normally sells thetype of item being supplied;
(3) Takes ownership or possession of the item(s) with its personnel, equipment or facilities in a manner consistent with industry practice; and
(4) Will supply the end item of a small business manufacturer, processor, or producer made in the United States.

NIH must receive written capability statements no later than December 7, 2017 at 9:00 a.m. Eastern Time. E-mail the written capability statement to Lisa Schaupp, the Contract Specialist, at the e-mail address Lisa.Schaupp@nih.gov.

Respondents will NOT be notified as to the results of the Government's market research.

CITE: https://www.fbo.gov/spg/HHS/NIH/CCOPC/NIH-CC-18-002793/listing.html