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Accompanying patient consent form to the frontline requisition form (only applicable in relevant states).
Tempus’ patient consent form for genomic testing, for international use.
Tempus’ patient consent form for genomic testing, for international use (EU/UK specific).
Tempus’ frontline order requisition form, for international use.
A de-identified version of Tempus’ frontline order requisition form, for international use.
A form containing supplemental information required for Tempus’ xG Hereditary Cancer Panel.
Tempus’ order requisition form for the Lilly Lung Cancer NGS Program.
Tempus’ order requisition form for the Lilly Lung Cancer NGS Program, NYS specific.
Tempus’ order requisition form for the Lilly Thyroid Cancer NGS Program.
Tempus’ order requisition form for the Lilly Thyroid Cancer NGS Program, NYS specific.
Tempus’ order requisition form for Neurology & Psychiatry assays.
Formulario de consentimiento del paciente adjunto al formulario de solicitud principal (solo aplicable en los estados pertinentes).
Tempus’ notice and authorization for health records form.
Tempus' financial assistance policy based on household income levels.
A guide designed to help you complete Tempus’ frontline requisition form.
An outline of Tempus’ state-of-the-art CAP-accredited and CLIA-certified sequencing lab equipment.
Tempus’ specimen collection guidelines for Life Sciences partners only.
Specimen collection instructions for Tempus’ COVID Nasal Collection kit.
Tempus’ iC SARS-CoV-2 Test FDA fact sheet for Healthcare Providers.
SalivaDirect’s Pro funnel collection instructions.
SalivaDirect’s Home funnel collection instructions.
FDA Emergency Use Authorization letter for SalivaDirect tests (Home/Pro).
FDA Emergency Use Authorization summary for SalivaDirect tests (Home/Pro).
For Clinical Trial Use: Regulatory labeling requirement and description of the CE marked and ISO 13485 compliant version of the xT assay (DNA).
For Clinical Trial Use: Regulatory labeling requirement and description of the CE marked and ISO 13485 compliant version of the xT assay (RNA).
Detailed information regarding the FDA approval of xT CDx.
Tempus’ patient information brochure for Neurology & Psychiatry.
Folleto de información al paciente para los exámenes de Neurología y Psiquiatría de Tempus.
Tempus’ no-surprise billing policy for our Neurology & Psychiatry assays.
A guide designed to help you understand Tempus’ hereditary panels’ clinical reports.
An overview of Tempus’ liquid biopsy assay for clinical audiences.
Medicare's Laboratory Date of Service Policy, also known as the "14 day rule," determines whether Tempus bills Medicare or its hospital customers for laboratory tests provided to Medicare patients.
A panel of genes detected by Tempus’ xT assay, New York State specific.
A panel of genes detected by Tempus’ xF assay, New York State specific.
The latest validation summary for Tempus’ xT assay, New York State specific.
The latest validation summary for Tempus’ xF assay, New York State specific.
