Inactive

RFI Amendment 1 to change response due date from 6-23-21 to 6-28-21, 12 noon EST, See attached.

Inactive

STRATEGIC SOURCING, BLOOD AND BLOOD PRDUCTS Purpose and Objectives: The intent of this Sources Sought Notice is to identify potential businesses capable of providing Blood and Blood Products as listed... STRATEGIC SOURCING, BLOOD AND BLOOD PRDUCTS Purpose and Objectives: The intent of this Sources Sought Notice is to identify potential businesses capable of providing Blood and Blood Products as listed in the below Statement of Need. It is expected that NAICS Code 621991, Blood and Organ Banks will be used for this solicitation. This product has the potential to be used throughout the VISN 4 Medical Centers listed below. Vendors to this Sources Sought Notice shall demonstrate the firm's ability, capability, and responsibility to provide the principal Blood and Blood Products listed below. Vendors shall indicate which of the VISN 4 VA Medical Centers listed below they can adequately service. Vendors shall include the following information: Business name, address, Point of Contact, Business size. Vendors shall indicate whether they are certified and accredited in the standards listed below. Vendors shall indicate if they are the direct supplier of the items. All information is to be submitted via e-mail at ronald.kline@va.gov. Information provided will not be returned. All responses shall be in the English Language. Responses are due by 12:00 pm (ET) on Wednesday, June 23, 2021. No submissions will be accepted after this date and time. Questions can be submitted electronically to ronald.kline@va.gov. This is a Sources Sought Notice and submissions will be used for informational and planning purposes only. This notice does not constitute a formal Request for Quote (RFQ), nor is the government obligated to issue an RFQ. In addition, the Government does not intend to pay for any information provided under this notice. The Government is not obligated to notify respondents of the results of this survey either. VISN 4 VA Medical Centers: Altoona VAMC 2907 Pleasant Valley Blvd. Altoona, PA 16602 Coatesville VAMC 1400 Black Horse Hill Road Coatesville, PA 19320 Erie VAMC 135 East 38th Street Erie, PA 16504 Lebanon VAMC 1700 South Lincoln Ave. Lebanon, PA 17042 Philadelphia VAMC 3900 Woodland Ave. Philadelphia, PA 19104 Butler VAMC 325 New Castle Road Butler, PA 16001 Pittsburgh VAMC 1010 Delafield Road Pittsburgh, PA 15215 Wilkes-Barre VAMC 1111 East End Blvd. Wilkes-Barre, PA 18711 Wilmington VAMC 1601 Kirkwood Hwy Wilmington, PA 19805 BLOOD SUPPLIER STATEMENT OF WORK I. PURPOSE: The vendor will be required to provide Blood/ Blood Products for various VISN 4 VA Medical Centers. They will need to provide Reference Laboratory services for any additional patient testing for difficult antibody workup or problems with incompatible blood with help in finding antigen negative units. II. REQUIREMENTS: 1. The vendor shall meet the standards of all licensing and accreditation agencies to include the following: College of American Pathologist (CAP), Occupational Safety and Health Administration (OSHA), Food & Drug Administration (FDA), and American Association of Blood Banks (AABB). 2. The vendor shall be able to supply the following products: Blood Product List Whole Blood Whole Blood Whole Blood Autologous Whole Blood Directed Whole Blood Irradiated Whole Blood Leuko Reduced Whole Blood Leuko Reduced Irradiated Whole Blood Leuko Reduced Autologous Whole Blood Leuko Reduced Directed Whole Blood Leuko Reduced Autologous Irradiated Whole Blood Leuko Reduced Directed Irradiated Red Blood Cells Leuko Reduced Red Blood Cells Leuko Reduced Red Blood Cells Irradiated Leuko Reduced Red Blood Cells Autologous Leuko Reduced Red Blood Cells Directed Leuko Reduced Red Blood Cells Autologous Irradiated Leuko Reduced Red Blood Cells Directed Irradiated Washed Red Blood Cells Washed Red Blood Cells Irradiate Deglyced Red Blood Cells Frozen RBC Plasma Fresh Frozen Plasma (FFP) Fresh Frozen Plasma < 6 hours (FP6) Fresh Frozen Plasma <24 hours (FP24) Liquid Plasma Cryo Reduced Plasma Platelets Leuko Reduced Single Donor Platelets (SDP) Leuko Reduced Single Donor Platelets (SDP) Irradiated Leuko Reduced Single Donor Platelets (SDP) Irradiated Directed Leuko Reduced Plasma Reduced Platelets (PR Platelets) Leuko Reduced Platelet Addidive Solution Platelets (PASC Platelets) Leuko Reduced Platelet Addidive Solution Platelets (PASC Platelets) Irradiated Leuko Reduced Bacterial Monitored<36 hours (LVDS 36) Leuko Reduced Bacterial Monitored<36 hours (LVDS 36) Irradiated Pooled Platelets Cryoprecipatate Cryoprecipatate Pool Cryoprecipitate Convelascent Plasma Convalescent Plasma 3. The Vendor shall provide directed donation service specifically for the needs provided a Directed Donation Blood Prescription when submitted by the requesting physician. The units drawn shall be separated into component parts; the component ordered shall be tagged for identification and shipped to the VISN 4 Medical Centers and upon completion of testing provided it is compatible with the patient. 4. The Vendor shall service autologous donors provided an Autologous Blood Prescription by the requesting physician and the donor meets the blood supplier standards for autologous donors. The units of blood drawn shall be tested and sent to VISN 4 Medical Centers upon completion of testing. 5. The Vendor shall provide Patient Immunohematology Reference Testing to include any special testing that may be needed. Such testing would be for identification of Antibodies, Compatibility Testing, antigen negative units when indicated. Testing may not be limited to this. 6. The Vendor shall abide by all security and integrity of the patient information per the HIPAA regulations. 7. The Vendor shall provide set-up a schedule for routine deliveries. III. PROCEDURES 1. Blood Products ordered shall set a routine delivery schedule that will be coordinated with the site. 2. The government shall receive full credit for expired red cells or any blood product that is found to be unsuitable for use. 3. The Vendor shall accept any blood unsuitable for Transfusion, Recall, Withdrawals and Transfers. IV. PERFORMANCE STANDARDS Description Para ref Standard Routine Delivery III,1. On time delivery 95% Directed & Autologous Donation III,3.& 4. Phlebotomy performed per request 100% Reference Lab Patient Test results & Interpretations II, 5 Patient testing work-up completed in a timely manner 100% License II,1. Documentation of all required licensing 100% Security II,6. Abide by all HIPAA regulations 100% Recalls/Non-conforming products III,4. All recalls and non-conforming notifications will be provided as deemed y the accreditation service 100% NARA Records Management Language for Contracts Required The following standard items relate to records generated in executing the contract and shall be included in a typical Electronic Information Systems (EIS) procurement contract: 1. Citations to pertinent laws, codes and regulations such as 44 U.S.C chapters 21, 29, 31 and 33; Freedom of Information Act (5 U.S.C. 552); Privacy Act (5 U.S.C. 552a); 36 CFR Part 1222 and Part 1228. 2. Vendor shall treat all deliverables under the contract as the property of the U.S. Government for which the Government Agency shall have unlimited rights to use, dispose of, or disclose such data contained therein as it determines to be in the public interest. 3. Vendor shall not create or maintain any records that are not specifically tied to or authorized by the contract using Government IT equipment and/or Government records. 4. Vendor shall not retain, use, sell, or disseminate copies of any deliverable that contains information covered by the Privacy Act of 1974 or that which is generally protected by the Freedom of Information Act. 5. Vendor shall not create or maintain any records containing any Government Agency records that are not specifically tied to or authorized by the contract. 6. The Government Agency owns the rights to all data/records produced as part of this contract. 7. The Government Agency owns the rights to all electronic information (electronic data, electronic information systems, electronic databases, etc.) and all supporting documentation created as part of this contract. Vendor must deliver sufficient technical documentation with all data deliverables to permit the agency to use the data. 8. Vendor agrees to comply with Federal and Agency records management policies, including those policies associated with the safeguarding of records covered by the Privacy Act of 1974. These policies include the preservation of all records created or received regardless of format [paper, electronic, etc.] or mode of transmission [e-mail, fax, etc.] or state of completion [draft, final, etc.]. 9. No disposition of documents will be allowed without the prior written consent of the Contracting Officer. The Agency and its contractors are responsible for preventing the alienation or unauthorized destruction of records, including all forms of mutilation. Willful and unlawful destruction, damage or alienation of Federal records is subject to the fines and penalties imposed by 18 U.S.C. 2701. Records may not be removed from the legal custody of the Agency or destroyed without regard to the provisions of the agency records schedules. 10. Vendor is required to obtain the Contracting Officer's approval prior to engaging in any contractual relationship (sub-contractor) in support of this contract requiring the disclosure of information, documentary material and/or records generated under, or relating to, this contract. The Vendor (and any sub-contractor) is required to abide by Government and Agency guidance for protecting sensitive and proprietary information. DISCLAIMER This RFI is issued solely for information and planning purposes only and does not constitute a solicitation. All information received in response to this RFI that is marked as proprietary will be handled accordingly. In accordance with FAR 15.201(e), responses to this notice are not offers and cannot be accepted by the Government to form a binding contract. Responders are solely responsible for all expenses associated with responding to this RFI. End of Document