Radiopharmaceutical-Fresno-DESCRIPTION-.pdf

The Department of Veterans Affairs, Network Contracting Office (NCO 21) has a requirement for Radiopharmaceuticals for the VA Central California Healthcare System (VACCHCS) located in Fresno, CA. The Government intends on awarding a single-award Indefinite Delivery

Indefinite Quantity (IDIQ) contract.

The scope of requirements includes:

Anticipated Supplies required based on historical usage:

Item 1-hr

Delivery Est #

UD

Est # mCi

Units

C-14 Carbon-14 urea kit (including H Pylori Breath Test Analysis) 2 kit

F-18 FDG Fludeoxyglucose UD 0 UD

Ga-67 (Gallium Citrate) (~0.080 mCi per UD) 2 0.16 mCi

Ga-67 (Gallium Citrate) (~6 mCi per UD) 2 12 mCi

Ga-67 (Gallium Citrate) (~9 mCi per UD) 2 18 mCi

I-123 (Sodium Iodide I-123 Capsule) (0.2 mCi capsule) 10 UD

I-123 (Sodium Iodide I-123 Capsules) (4 mCi capsule) 2 UD

I-123 Iobenguane Sulfate; I-123 MIBG (Adreview) UD 0 UD

I-131 (Sodium Iodide Compounded Capsules) per first 6 mCi each order 5 UD

I-131 (Sodium Iodide Compounded Capsules) per ~1-2 mCi capsule 0

I-131 (Sodium Iodide Compounded Capsules) per ~10-15 mCi capsule 2 30 mCi

I-131 (Sodium Iodide Compounded Capsules) per ~30 mCi capsule 1 30 mCi

I-131 (Sodium Iodide Compounded Capsules) per ~100 mCi capsule 2 200 mCi

In-111 Capromab Pendetide (Prostascint) UD 0 UD

In-111 Pentetreotide (Octreoscan®) UD 4 UD

Sm-153 Lexidronam (Quadramet®) ~100 mCi UD 1 UD

Sr-89 Strontium Chloride UD 1 UD

Tc99m Bicisate Dihydrochloride (Neurolite®) UD 0 UD

Tc99m Disofenin UD 0 UD

Tc99m DTPA (Pentetate) [15 mCi for injection] UD 5 UD

Tc99m DTPA ~45 mCi Pulmonary [for aerosol] UD 30 UD

Tc99m Ceretec (Exametazime aka HMPAO) UD {brain study} 0 UD

Tc99m HDP (Oxidronate) UD 0 UD

Tc99m MAA (Macroaggregated Albumin) UD 30 UD

Tc99m MDP (Medronate) UD 200 UD

Tc99m Mebrofenin (Choletec) UD 45 UD

Tc99m Mertiatide (MAG3) UD 20 UD

Tc99m NaTc04 UD (~25-35 mCi) 40 UD

TC99m NaTc04-QC; syringe (~10 mCi per UD) 2 UD

TC99m NaTc04-QC; VIAL (~250 mCi per vial) 4 1000 mCi

Tc99m PYP (Pyrophosphate) UD 0 UD

Tc99m Sestamibi-Generic UD

UD

Tc99m Sestamibi as Cardiolite UD UD

Tc99m Tetrofosmin (Myoview) UD UD

Lidocaine dilution for sulfur colloid intradermal injection 8 ea

Tc99m Sulfur Colloid Filtered UD (~0.5 mCi per UD) 20 UD

Tc99m Sulfur Colloid UD (~1 mCi per UD) (oral) 4 UD

Tc99m Sulfur Colloid UD (~10 mCi per UD) 4 UD

Tl-201 (Thallous Chloride) UD (1 mCi per UD) 2 2 UD

Tl-201 (Thallous Chloride) UD (4 mCi per UD) 10 40 UD

Sn-PYP (Pyrophosphate) VIAL for Labeling Red Blood Cells (per vial) 0 ea

UltraTag® VIAL for Labeling Red Blood Cells (per vial) 15 ea

Labeled WBC (autologous leukocytes) In-111 Oxine (Oxyquinoline) UD 5 UD

Labeled WBC (autologous leukocytes) In-111 Chloride (Tropolone) UD 1 UD

Labeled WBC (autologous leukocytes) Tc99m Ceretec (Exametazime HMPAO)

UD 1 UD

WBC blood-tag Kit 7 ea

The contractor agrees to deliver routine and non-routine radiopharmaceuticals to VA Central

California Health Care System (VACCHCS) on a daily basis.

Have processes in place to ensure timely and flexible delivery of radiopharmaceuticals.

Contractor shall deliver routine pharmaceuticals before the beginning of the workday (before

8:00 a.m., Monday – Friday, excluding Federal holidays). Deliver planned intra-day radiopharmaceutical deliveries at contractor’s convenience as long as arrival is more than 15 minutes before the patient’s scheduled appointment time, as indicated on the dose order form

(Note: Patient arrival-time is earlier than the radiopharmaceutical calibration-time). For unscheduled intra-day orders, deliver routinely available radiopharmaceuticals generally within one-hour and not more than two-hours from the time of order.

Contractor must be licensed by the Nuclear Regulatory Commission and be regularly established in the business of providing radiopharmaceuticals. Offeror must provide copies of licenses and certifications along with quote to the Contracting Officer.

Contractor shall perform all quality control procedures as required by Federal and State regulatory agencies and Joint Commission.

All shipments must be compliant with all Nuclear Regulatory Commission and Department of

Transportation packaging and transport regulations.

Contractor shall meet all Nuclear Regulatory Commission, Department of Transportation, FDA, OSHA and all other agency rules and regulations (Federal and State).

The North American Industry Classification (NAICS) code is 325412, Pharmaceutical

Preparation Manufacturing, size standard 1,250 employees. Potential Offerors must register at the Contract Opportunities website https://beta.sam.gov to obtain direct access to any posted project documents. Registration instructions can be found on the beta.sam.gov website. It is the responsibility of the Offeror to check the beta.sam.gov website periodically for any revisions to the posted documents. All prime firms are required to complete the System for Award

Management (SAM) via the website at https://beta.sam.gov.