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This Sources Sought opportunity was posted on March 16, 2004. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

65--Asthma Protocol Supplies - Standardization

Closed
W81K02-04-T-CAREFederal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

Active Opportunities Like This One

NAICS: 423450
New
SLED
First Aid Suplies
Solicitation # 26-CR-043
Solicitation 26-CR-043, issued by the School Board of Pinellas County, seeks suppliers to provide and deliver first aid supplies on an as-needed basis to the Walter Pownall Service Center Warehouse in Largo, Florida. The contract requires firm net pricing and F.O.B. Destination delivery with freight included. Deliverables include a wide range of medical supplies such as vinyl exam gloves, sterile bandages, cotton-tipped applicators, and infrared thermometers. Specific packaging requirements are mandated for various items, and certain products must be sterile and individually wrapped. Bidders offering alternate products must provide exact samples using the required District labels and, in the case of infrared thermometers, provide FDA certification. The award will be granted to the bid judged most beneficial to the District, with a 5 percent preference given to responsive bidders based in Florida. Bids that include minimum order requirements will be deemed non-responsive. Required submission documents include a Drug Free Workplace Certification, Debarment Form AD-1048, a Prohibition Against Coercion for Labor and Services Affidavit, and a Bidder’s Statement of Principal Place of Business. Additionally, the successful contractor must obtain all required insurance within ten working days of the award, naming the School Board of Pinellas County as an additional insured and certificate holder. Personnel must comply with the Jessica Lunsford Act, requiring Level 2 background screening, including fingerprinting and criminal record checks through the FDLE and FBI.
Purchasing

POSTED

about 14 hours ago

DEADLINE

in 24 days

AI Contract Overview

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TRICARE Pacific Region 12 is seeking sources to participate in the regional standardization of Asthma Protocol Supplies for military medical treatment facilities located in Hawaii, Japan, Okinawa, Korea, and Guam. The required product line consists of aerosol nebulizers, peak flow meters, and pediatric valved holding chambers. To be eligible, companies must currently hold or be in the process of obtaining a Distribution and Pricing Agreement with the Defense Supply Center-Philadelphia. Interested vendors must submit their company information and detailed responses to a series of technical and operational questions by April 6, 2004. These requirements include verification of FDA approval, latex-free status, availability through prime vendors, and adherence to specific clinical standards such as those from the American Thoracic Society and the National Asthma Education Prevention Program. Additionally, vendors are required to provide product literature via FedEx or UPS to the Tricare Pacific Lead Agency.

General Info

TRICARE Pacific seeks asthma protocol supply vendors for military facilities in Pacific regions.

Agency

N/A

NAICS

423450 - Medical, Dental, and Hospital Equipment and Supplies Merchant Wholesalers

Place of Performance

Tri-Service Regional Business Office, TRICARE Pacific Region 12 Attn: Cheryl Janus, MCHK-LA, 1 Jarrett White Road Tripler AMC H

Set-Aside

NONE

Documents

0

No documents available

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Timeline

PhaseClosed
Posted

Sources Sought

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyN/A
ContactsNo contacts available
OfficeN/A
Organization / Agency
N/A
Office AddressN/A
ContactsNo contact information available

Full Description

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Potential sources sought to participate in the regional standardization of Asthma Protocol Supplies. TRICARE Pacific Region 12, a military integrated delivery network (IDN), comprised of Army, Navy, Air Force, Marine Corps and Coast Guard medical tre atment facilities in Hawaii, Japan, Okinawa, Korea and Guam are in the process of standardizing Asthma Protocol Supplies. This product line includes pediatric valved holding chambers for aerosol delivery of medication, aerosol nebulizers, and peak flow met ers. If your company currently holds or in the process of obtaining a Distribution and Pricing Agreement (DAPA) with the Defense Supply Center-Philadelphia (DSCP) Asthma Protocol Supplies, your company is eligible to participate in the standardization proc ess. Please respond by Email: contact@example.gov and provide your company name, address, point of contact, telephone, fax and E-mail address and answers to the below listed questions no later than April 6, 2004 1. Are your products available through the prime vendor Owens Minor or Cardinal? If yes, what is your DAPA number? 2. Under what brand(s) does your company manufacture or distribute your product? 3. Are your products latex free? 4. Under what standards are your products manufactured? 5. Are your products FDA approved? 6. That types of educational tools or materials do you have for this product line? 7. What kind of staff training does your company provide? 8. Does your company provide customer service 24/7? 9. Is there any history of backorders and/or recalls for this product group? If yes, please answer: a. Dates and duration, b. Cause, c. Resolution. Peak Flow Meter: (1) Does your company manufacture a peak flow meter? (2) Do your peak flow meters meet the most current American Thoracic Society Standards for Spirometry adopted in 1994 and the educational guidelines recommended by the National Asthma E ducation Prevention Program (NAEPP) of the National Institutes of Health? Aerosol Nebulizer: (1) Does your company manufacture a nebulizer that can be operated in both a continuous mode and/or breath-activated mode? If so, can this product be changed from mode to mode? (2) Has your product been published, peer reviewed, bench and/or clinically studied? If so, please list? Pediatric Valved Holding Chamber: (1) Does your company manufacture a line of pediatric valved holding chambers for all children aged bi rth to 17 years old? (2) Does your product meet CSA standards for drop testing? (3) Has your product been tested using USP methods normalizing the dose for the following pMDI formulations? a. Flovent 110 µg CFC and HFA formulations, b. Albuterol 90 µ g CFC and HFA formulations, c. Ipratropium Bromide 18 µg, d. Albuterol/ipratropium bromide combination (CombiVentO), (4) Are instructions for use of this product consistent with recommendations for Holding Chambers according to the AARC Clinical Practic e Guideline: Selection of an Aerosol Delivery Device for Neonatal and Pediatric Patients as published in Respiratory Care 1995; 40(12):1325-1335? Please FEDEX/UPS your product literature on Asthma Protocol Supplies by April 6, 2004 to: Ms. Cheryl A. Janus, RN, MBA, Tricare Pacific Lead Agency, 1 Jarrett White Road, MCHK-LA, Tripler, HI 96859-5000, Telephone: +1 (555) 000-0000

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