Automated Media Preparation Instrument for Dissolution Testing

The U.S. Food and Drug Administration (FDA), Irvine Medical Products Laboratory (IRVLMP), has a requirement for the purchase, delivery, installation, operator training, and warranty support of one (1) Automated Media Preparation Instrument for Dissolution Testing. This acquisition will be conducted as a brand-name-or-equal procurement under NAICS 334516. The instrument shall provide automated preparation of dissolution media for laboratory testing and be capable of heating, degassing, and dispensing dissolution media in accordance with the Government's minimum technical requirements. Salient characteristics include automated media preparation, precise dispensing accuracy, in-line heating, temperature control, media degassing capability, onboard programmable operation, reporting functionality, portability, compatibility with standard U.S. electrical service (115V, 50/60 Hz), and the ability to fill dissolution vessels while installed on dissolution apparatus. The Contractor shall furnish all labor, materials, equipment, transportation, installation, operator training, warranty support, documentation, and other resources necessary to provide a fully operational system. Installation shall be performed by an OEM-trained and certified field service engineer and shall include operational verification testing. Operator training for two (2) users shall be provided at the Government site. The Contractor shall provide a minimum twelve (12)-month manufacturer's warranty covering parts, labor, travel, technical support, and OEM-certified service. Required deliverables include the automated media preparation instrument, installation and qualification, operator training, service documentation, and warranty documentation. Delivery shall be completed within sixty (60) days after contract award. Installation shall be completed no later than thirty (30) days after delivery at the FDA Irvine Medical Products Laboratory, Irvine, California. Final Government acceptance will occur following successful delivery, installation, operational verification, completion of training, and confirmation that the equipment meets all requirements specified in the solicitation.

• NAICS334516
• PSC6632

No documents posted for this opportunity.

• Reagan Davis
  reagan.davis@fda.hhs.gov3017960910