FDA Grants Clearance to BD Molecular Test
FDA has granted premarket notification (510(k)) clearance to BD for its newly developed molecular test for detecting harmful intestinal bacteria causing infectious diarrhea.
Read MorePosted by Elaine Sanchez Wilson | Aug 7, 2017 | Molecular Diagnostics |
FDA has granted premarket notification (510(k)) clearance to BD for its newly developed molecular test for detecting harmful intestinal bacteria causing infectious diarrhea.
Read MorePosted by Elaine Sanchez Wilson | Aug 1, 2017 | Middleware & Software |
The agreement consists of a strategic expertise exchange between UgenTec and Hamann Laborautomation.
Read MorePosted by Elaine Sanchez Wilson | Aug 1, 2017 | Biochemicals & Chemical Reagents, Clinical Chemistry, Clinical Chemistry Analyzers, Clinical Chemistry Test Kits |
Beckman Coulter Diagnostics, along with partner Diazyme Laboratories, has announced FDA premarket notification (510(k)) clearance of a new procalcitonin assay.
Read MorePosted by Elaine Sanchez Wilson | Jul 17, 2017 | Molecular Diagnostics |
The Precision Diagnostics in Inflammatory Bowel Disease, Cellular Therapy, and Transplantation (PREDICT) trial is expected to provide clinicians new information about why inflammatory bowel disease arises in children, allowing them to tailor treatment plans to each patient.
Read MorePosted by Elaine Sanchez Wilson | Jul 17, 2017 | Cancer |
The clinical lab community needs a shared vision for calculating the value of diagnostic testing.
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