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Title: Environmental Monitoring and ISO 14644 Certification Services for NIH Center for Cellular Engineering (CCE) Classification Code (PSC): Q301 – Medical – Laboratory Testing NAICS Code: 621511 – Medical Laboratories Place of Performance: National Institutes of Health Clinical Center Bethesda, MD 20892 POTS: 26-004699 Description This notice is issued for informational purposes only and does not constitute a request for quotations. A solicitation will not be issued, and quotations will not be requested. The National Institutes of Health (NIH), Clinical Center, intends to award a sole source firm-fixed-price contract to American Certified LLC to provide environmental monitoring and certification services for the Center for Cellular Engineering facilities. These services include confirmation that air changes per hour, HEPA filter integrity, differential pressure between controlled rooms, and non-viable particulate levels comply with Food and Drug Administration (FDA) mandates and meet the established criteria outlined in ISO 14644. ISO 14644 defines the standards for cleanrooms used in aseptic processing and is critical to ensure patient safety by minimizing the risk of environmental contamination during the production of cell-based therapies. The anticipated period of performance is from 05/25/2026 to 10/25/2026 Background The Center for Cellular Engineering (CCE) manufactures cell-based therapies for patients who have no remaining or effective standard treatment options. These manufacturing operations are regulated under Current Good Manufacturing Practices (cGMP) as mandated by the Food and Drug Administration (FDA) in accordance with 21 CFR Parts 210, 211, 600, and 1271. This contract supports CCE's environmental monitoring program, which ensures that facilities used for aseptic processing of cell-based therapies for patients enrolled in NIH-sponsored clinical trials are certified as fit for use. The program includes routine sampling of facility air and surfaces to assess environmental conditions and detect the presence of microorganisms. Data collected through this program enables tracking and trending to identify potential issues with air handling systems and facility conditions before they impact patient therapies. These environmental monitoring activities are required by the FDA to ensure compliance with regulatory standards and to safeguard patient safety. The contractor shall provide environmental monitoring, testing, and certification services to ensure that the Center for Cellular Engineering (CCE) facilities meet the room classification standards established under ISO 14644 and are fit for aseptic processing operations. Required tasks include sampling air quality for non-viable particulates, performing viable and non-viable air sampling, calculating air changes per hour (ACH) for each critical room, conducting HEPA filter integrity testing, measuring differential pressures between controlled rooms to verify proper airflow and pressu…

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