Partner Veritas The most innovative Checkup: Genomic Checkup Veritas allows you to have a new concept of health check for your patients: Genomic Checkup. This model incorporates myGenome into your patients’ medical routine, including genomics to medical information. This approach achieves a greater capacity for prevention, since it allows the adaptation of medical check-ups in the future based on the genomic results of each patient. Some of the most prestigious health institutions already include this Genomic Checkup in their portfolio of services, placing themselves at the forefront of precision, predictive, preventive and personalized medicine. Experts in Genomics Veritas is The Genome Company, genomic analysis and interpretation are our specialty, we have experts with more than 15 years of experience in this field. Advice to the Professional We have a medical team expert in genomics applied to different medical areas to advise you when you need it. Innovation We develop new and innovative services that allow medical professionals to offer their patients the most innovative products in healthcare. Continuous Training We train our collaborators to be at the forefront in the tools that genomics makes available to them for the preventive care and management of their patients. Our services encompass four areas of genetics All our genetic tests require a genetic consultation to evaluate which of our services is suitable. Veritas can support this process by providing pre and post-test genetic counselling to assess what tests are suitable, the interpretation of results and, if necessary, the design of an action plan for future healthcare management.da. PREVENTIVE MEDICINE PREGNANCY AND EARLY CHILDHOOD DIAGNOSTIC GENOMICS GENETIC COUNSELLING The most comprehensive genetic service, based on whole genome sequencing, for disease prevention and healthcare. Polygenic risk screening for common diseases. Genetic test to assess the risk for common diseases. Non-invasive prenatal test that studies the most frequent chromosomal abnormalities. The most complete genetic care for your baby that brings together myPrenatal and myNewborn. Screening for early childhood onset diseases. Hereditary cancer prevention. Genome-based diagnostic service. Targeted studies designed for specific pathologies. Hereditary cardiovascular disease prevention. Exome-based diagnostic service. Genetic counselling and second opinion medical consultation on diseases with a hereditary origin. Why are genetics important in preventive healthcare management? 17% 17% of people have genetic variants that increase the risk of diseases. 20% Up to 20% of cancer cases are related to hereditary factors. 20% Around 20% of sudden cardiac deaths are due to genetic abnormalities. 5% 5% of patients are hospitalised for adverse drug reactions. 86% 86% of people are asymptomatic carriers of a monogenic disease that can be transmitted to their offspring if the partner is a carrier of the same disease. 9% Up to 9,4% of newborns may have genetic variants linked to early onset childhood diseases. Do you want to know more about our genetic services? Fill in the form and we will contact you for further information. We are experts in genetic sequencing and interpretation We support any organization, either as a distributor or prescriber of our products and services or having us as a partner in genetics in research projects.