SOLICITATION NOTICE
65 -- N68470-05-RQLC002
- Notice Date
- 2/9/2005
- Notice Type
- Solicitation Notice
- NAICS
- 621511
— Medical Laboratories
- Contracting Office
- Department of the Navy, Bureau of Medicine and Surgery, NH Okinawa, U. S. Naval Hospital Okinawa, Material Mgmt Dept PSC 482, Box 248, FPO, AP, 96362
- ZIP Code
- 96362
- Solicitation Number
- Reference-Number-N68470-05-RQLC002
- Response Due
- 2/25/2005
- Archive Date
- 3/12/2005
- Description
- This is a combined synopsis/solicitation for commercial items prepared in accordance with the format in Subpart 12.6, as supplemented with additional information included in this notice. This announcement constitutes the only solicitation; proposals are being requested and a written solicitation will not be issued. The reference number for this acquisition is RFP N68470-05-RQLC002. The incorporated provisions and clauses are those in effect through Federal Acquisition Circular 01-25. The associated North American Industry Classification System (NAICS) Code is 621511. The US Naval Hospital intends to award a firm-fixed price contract for the remainder of the 2005 Fiscal Year with 4 one-year options. Description of the class of products to be procured is New Born Screening for Analysis of New Born Blood Samples. Factors used to evaluate offers are lowest priced, technically acceptable with turn around/delivery time of lab results and availability of follow-up services and genetic counseling as a significant subfactor. Delivery and acceptance point shall be US Naval Hospital Okinawa, Bldg 6000 Camp Lester, Okinawa, Japan T904-0103. Offeror will be required to contact the government POC with results per delivery schedule. Description of Services: New born screening panel, at a minimum, shall include: Mass Spectrometry and Tandem Mass Spectrometry (MS/MS) Biotinidase 17-hydroxyprogesterone (Congential Adrenal Hyperplasia) Glucose-6-phosphate dehydrogenase deficiency (G6PD) Cystic fibrosis testing, immunoreactive trypsinogen: immunoassay for analyte other than infectious agent, multiple step method Thyroid Stimulating Hormone (TSH) Hemoglobin fractionation, electrophoresis Galactose Galactose-1-phosphate uridyltransferase, screen Spectrum of testing of all samples, at a minimum, shall include: Fatty Acid Oxidation Disorders Carnitine/Acylcarnitine Translocase Deficiency (Translocase) Carnitine Palmitoyl Transferase Deficiency Type I (CPT-I) 2,4-Dienoyl-CoA Reductase Deficiency 3-Hydroxy Long Chain Acyl-CoA Dehydrogenase Deficiency (LCHAD) Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Multiple Acyl-CoA Dehydrogenase Deficiency (MADD or Glutaric Acidemia-Type II) Neonatal Carnitine Palmitoyl Transferase Deficiency-Type II (CPT-II) Short Chain Acyl-CoA Dehydrogenase Deficiency (SCAD) Short Chain Hydroxy Acyl-CoA Dehydrogenase Deficiency (SCHAD) Trifunctional Protein Deficiency (TFP Deficiency) Very Long Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD) Organic Acid Disorders 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (HMG) Glutaric Acidemia-Type I (GA I) Isobutyryl-CoA Dehydrogenase Deficiency Isovaleric Acidemia (IVA) Acute onset Chronic 2-Methylbutyryl-CoA Dehydrogenase Deficiency 3-Methylcrotonyl-CoA Carboxylase Deficiency (3MCC Deficiency) 3-Methylglutaconyl-CoA Hydratase Deficiency Methylmalonic Acidemias Methylmalonyl-CoA Mutase Deficiency 0 Methylmalonyl-CoA Mutase Deficiency + Some Adenosylcobalamin Synthesis Defects Maternal Vitamin B12 Deficiency Mitochondrial Acetoacetyl-CoA Thiolase Deficiency (3-Ketothiolase Deficiency) Propionic Acidemia (PA) Acute onset Late onset Malonic Aciduria Multiple CoA Carboxylase Deficiency Amino Acid Disorders Argininemia Argininosuccinic Aciduria (ASA Lyase Deficiency) Acute onset Late onset Carbamoylphosphate SynthetaseDeficiency (CPS Deficiency) Citrullinemia (ASA Synthetase Deficiency) Acute onset Late onset Homocystinuria Hypermethioninemia Hyperammonemia, Hyperornithinemia, Homocitrullinemia Syndrome (HHH) Hyperornithinemia with Gyral Atrophy Maple Syrup Urine Disease (MSUD) Classical MSUD Intermediate MSUD 5-Oxoprolinuria (Pyroglutamic Aciduria) Phenylketonuria (PKU) Classical PKU Hyperphenylalaninemia Biopterin Cofactor Deficiencies (4) Tyrosinemia Transient Neonatal Tyrosinemia Tyrosinemia Type I (Tyr I) Tyrosinemia Type II (Tyr II) Tyrosinemia Type III (Tyr III) Other Disorders Biotinidase Deficiency Complete Deficiency Partial Deficiency Cogenital Adrenal Hyperplasia Salt Wasting 21-Hydroxylase Deficiency Simple Virilizing 21-Hydroxylase Deficiency Glucose-6-Phosphate Dehydrogenase Deficiency Cystic Fibrosis Method of Notification of Test Results: Via facsimile and/or secure internet for routine results. Via telephone and/or facsimile for abnormal results. The Government will provide the transport of routine samples from Naval Hospital Okinawa to the Contractor?s Laboratory. This solicitation incorporates the following FAR Provisions: 52.204-6 Data Universal Numbering System (DUNS) Number; 52.212-1 Instruction to Offerors -- Commercial Items; 52.212-4 Contract Terms and Conditions -- Commercial Items; and 52.212-5 Contract Terms and Conditions Required to Implement Statutes or Executive Orders --Commercial Items. All responsible sources must submit a completed copy of the provision at FAR 52.212-3, Offeror Representations and Certifications ? Commercial Items with its offer. Closing Date: 5PM Eastern Standard Time (EST), 25 Feb 2005 Via Mail: US Naval Hospital, MMD, PSC 482 Box 248, FPO AP 96362-1695 Via E-Mail: KoslowskyM@oki10.med.navy.mil or OshiroHiro@oki.10.med.navy.mil Via Facsimile: +81-98-892-8574 or +81-98-893-5754 Anticipated Date of Award: 4 Mar 2005 Points of Contact: Mary Koslowsky at 011-81-611743-7556 or Hiro Oshiro at 011-81-611743-7412.
- Place of Performance
- Address: US Naval Hospital Okinawa,, Bldg 6000 Camp Lester,, Chatan-Cho, Okinawa
- Zip Code: 904-0103
- Country: Japan
- Zip Code: 904-0103
- Record
- SN00748587-W 20050211/050209212049 (fbodaily.com)
- Source
-
FedBizOpps.gov Link to This Notice
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