Forms & Documents
Test Requisition Forms (TRF) & Consent Forms
Test Requisition Forms (TRF) - US
General Test Requisition Form
Beacon Carrier Screening Requisition Form
Chromosomal Sequencing Analysis (CSA) Requisition Form
Newborn Genetic Analysis (NGA) Requisition Form
Hereditary Cancer Comprehensive Test Requisition Form
Hereditary Cancer Focus Test Requisition Form
Pharmacogenomics (PGx) Test Requisition Form
COVID-19 Plus Influenza A&B Test Requisition Form
Consent Forms - US
Informed Consent for Genetic Testing
Informed Consent for Genetic Testing (Spanish)
Informed Consent for Beacon Carrier Screening
Informed Consent for Chromosomal Sequencing Analysis (CSA)
Informed Consent for Newborn Genetic Analysis (NGA)
Informed Consent for Prenatal Genetic Testing
Consent Forms - NY Approved Tests
Informed Consent for Genetic Testing - Fulgent Clinical Exome Sequencing
Test Requisition Forms (TRF) - EU/EEA
General Test Requisition Form - EU/EEA
Beacon Carrier Screening Requisition Form - EU/EEA
Chromosomal Sequencing Analysis (CSA) Requisition Form - EU/EEA
Consent Forms - EU/EEA
Informed Consent for Genetic Testing - EU/EEA
Informed Consent for Genetic Testing - EU/EEA (Spanish)
Informed Consent for Beacon Carrier Screening - EU/EEA
Informed Consent for Chromosomal Sequencing Analysis (CSA) - EU/EEA
Informed Consent for Newborn Genetic Analysis (NGA) - EU/EEA
Informed Consent for Prenatal Genetic Testing - EU/EEA
Family History Forms
Family History of Medical Concerns
Patient Family Resources
Family Follow-up Testing Letter
Carrier Screening Documents
Family Letter
Raw Request Forms
Raw Data Request Instructions
Insurance Forms
Insurance Forms
Aetna BRCA Precertification Request Form
Application For Economic Hardship
Benefits Investigation Request Form
Cigna Genetic Testing Recommendation Form
Financial Assistance Disclosure Form
UHC Genetic Counseling Attestation Form
Medicare Criteria
Advance Beneficiary Notice of Noncoverage (ABN)
Breast-Ovarian Cancer BRCA1-BRCA2 Medicare Criteria Form
Hereditary Colorectal Cancer Lynch Syndrome Medicare Criteria Form
Letters of Medical Necessity
Aicardi-Goutieres
Alagille
Amyotrophic Lateral Sclerosis
Arrhythmia
Arrhythmogenic Right Ventricular Cardiomyopathy
Ataxia with Oculomotor Apraxia Type 1/2
Atrial Fibrillation
Autism
Basal Ganglia Calcification
Beacon Carrier Screening
Brugada Syndrome
Catecholaminergic Polymorphic Ventricular Tachycardia
Ciliopathies
Clinical Exome
Comprehensive Cancer
Congenital Sucrose Isomaltose Deficiency
Connective Tissue
Cornelia de Lange Syndrome
Dilated Cardiomyopathy
Early Onset Epilepsy
Essential Epilepsy
Hearing Loss
Holoprosencephaly
Idiopathic Epilepsy
Intellectual Disability
Joubert Syndrome
Joubert and Meckel
Marfan Syndrome, Thoracic Aortic Aneurysm & Dissection
Noonan Syndrome
Nuclear-Mito
Periodic Fever/Autoinflammatory Disorders
Polycystic Kidney Disease
Polycythemia Erythrocythemia
Skeletal Dysplasias
XLID
Questions?
Contact us at
info@fulgentgenetics.com
or
+1 (626) 350-0537
for more information.