Statement of Work- OC-2026-136029- Final.docx

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Procurement of Benchtop Environmental Temp/Humidity Chamber
Solicitation number
OC-2026-136029
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This is a Statement of Work for the procurement of a benchtop environmental temperature and humidity conditioning chamber for the FDA laboratory at the Winchester Engineering Analytical Center (WEAC). The chamber will be used to condition regulatory samples such as tampons, gowns, and patches at specific temperature and humidity levels prior to physical testing, and will support CDRH-directed research and test method development for medical devices analyzed under the Federal Food, Drug, and Cosmetic Act.

The environmental chamber must meet the following minimum specifications: temperature range of at least -20°C to 180°C; humidity range of 10% to 95% relative humidity; 4 cubic foot capacity; standard power cord and plug (no hardwiring required); easily accessible water supply connection; solid-state humidity sensor; water leak containment and detection system; viewing window for sample monitoring; at least one internal shelf; mobile cart with space-saving footprint due to limited laboratory space; at least one 2-inch diameter cable port with flexible plug; factory calibration or instrument calibration at start-up with ISO 17025 certificate; and minimum one-year on-site warranty. The contractor must provide newly manufactured components, on-site installation and commissioning, and warranty coverage for parts and labor for a minimum of 12 months from the date of formal government acceptance, including unlimited telephone and email support. The procurement also requires compliance with Section 508 accessibility requirements, including WCAG 2.0 A and AA standards for electronic content and support documentation.

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Statement of Work Environmental Chamber for Temperature and Humidity Conditioning of regulatory samples prior to testing.

Background The FDA laboratory at WEAC uses an environmental chamber to condition regulatory samples (such as tampons, gowns, patches, etc.) at specific temperature and humidity levels before physical testing. The chamber also supports CDRH-directed research and test method development for other medical devices received by the laboratory for analysis.

The laboratory analyzes medical devices under the Federal Food Drug and Cosmetic Act. Some products, such as tampons, are subject to the Code of Federal Regulations (CFR) performance standards, while others are tested against consensus standards or manufacturer’s specifications. Because of this variety, the laboratory requires a wide range of temperature and humidity conditions.

The current environmental chamber is over 15 years old. It has required costly repairs in recent years and experienced extended periods of downtime due to funding constraints and approval delays. A new environmental chamber will ensure that our capabilities remain consistently available.

General Requirements The contractor shall provide an environmental chamber that uniformly conditions samples across a variety of temperature and humidity settings. The chamber must meet the following specifications:

1. Temperature range: at least -20°C to 180°C

2. Humidity range: 10% to 95% relative humidity (RH)

3. Capacity: 4 cu. Ft.

4. Power: Standard power cord and plug (no hardwiring)

5. Water supply: Easily accessible water supply connection

6. Humidity sensor: Solid-state humidity sensor

7. Leak Detection: Must have a water leak containment and detection system

8. Viewing window: For visual monitoring of samples

9. Interior shelf: At least one internal shelf

10. Mobility: Mobile cart with space-saving footprint (lab has no bench space and limited floor space for the chamber)

11. Cable port: At least one 2-inch diameter cable port with a flexible plug

12. Calibration: Factory calibration with an ISO 17025 certificate, or instrument calibration at start-up with ISO 17025 certificate

13. Warranty: At least one year On-site Installation, Training and Commissioning

1. On-site installation and commissioning of the Environmental Chamber Trade and Service Specification

1. All components shall be newly manufactured, not used or refurbished, and/or previously used for demonstration.

2. System installation shall occur after being received at the laboratory.

3. The entire system shall be warranted for parts and labor for a minimum of 12 months from date of formal government acceptance after on-site installation.

4. The warranty must include unlimited telephone/e-mail support for questions regarding operation.

Additional Section 508 Requirements:

· Must meet WCAG 2.0 A and AA

· E101.2 Equivalent Facilitation (Appendix A, Application and Scoping Requirements)

· E203 Access to Functionality (Appendix A, Application and Scoping Requirements)

· E204 Functional Performance Criteria (Appendix A, Application and Scoping Requirements)

· E205 Electronic Content (Appendix A, Application and Scoping Requirements)

· 302 Functional Performance Criteria (Appendix C, Functional Performance Criteria and Technical Requirements)

· Electronic content must be accessible to HHS acceptance criteria. Checklist for various formats are available at https://www.hhs.gov/web/section-508/making-files-accessible/index.html, or from the Section 508 Coordinator listed at https://www.hhs.gov/web/section-508/additional- resources/section-508-contacts/index.html. Materials that are final items for delivery should be accompanied by the appropriate checklist, except upon approval of the Contracting Officer or Representative.

· E208 Support Documentation and Services (Appendix A, Application and Scoping Requirements)

· Chapter 6 Support Documentation and Services (Appendix C, Functional Performance Criteria

· E206 Hardware (Appendix A, Application and Scoping Requirements)

· Chapter 4 Hardware (Appendix C, Functional Performance Criteria and Technical Requirements) and Technical Requirements)

· E207 Software (Appendix A, Application and Scoping Requirements)

· Chapter 5 Software (Appendix C, Functional Performance Criteria and Technical Requirements)

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