hCG Testing - Immunoassay for FDA Approval
Project Description
MULTIPLE SAMPLES
We are currently preparing for FDA approval and need to conduct comparison testing using the Beckman Coulter Access 2 immunoassay system. Specifically, we are looking to process approximately 250–300 human chorionic gonadotropin (hCG) samples on the system. This would be a self-pay arrangement, with no insurance billing involved. If your lab is equipped with the Beckman Coulter Access 2 or any FDA-approved device and can support this type of testing, I would greatly appreciate the opportunity to discuss the next steps with you.
Thank you, and I look forward to your response.
Project Information
Number:25-01150
Industry:Clinical Diagnostic
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