Noninvasive Prenatal Testing (NIPT): We offer noninvasive prenatal testing to screen for chromosomal abnormalities in a developing fetus using a simple blood sample from the mother, providing a safe and reliable option for expectant parents.
Carrier Screening: We provide carrier screening tests to detect genetic mutations that could be passed on to offspring, helping families make informed reproductive decisions.
Molecular Diagnostics: Our molecular diagnostic tests cover a wide range of conditions, providing critical insights for the diagnosis and management of genetic disorders.
Research and Development: As a continuous innovation through robust research and development efforts. We stay at the forefront of genetic testing technologies, ensuring that our clients benefit from the latest advancements in the field.
Something about what they are doing now.
something about how they want to add genetics.
high level summary about how we intend to bring genetics into their existing laboratory.
Hosting regular onsite visits to educate doctors on the benefits and applications of using the in-house laboratory for genetic testing helps with physician adoption of the newly built genetic laboratory.
We offer one-on-one or small group training sessions to familiarize doctors with the lab’s testing capabilities and processes. as well as demonstrations on how to order tests, interpret results, and incorporate genetic testing into patient care.
Assigning a dedicated support team to work closely with doctors, addressing their questions and concerns promptly.
Provide direct access to genetic counselors and lab specialists for consultations.
Maintain regular communications through newsletters, email updates, and webinars to keep doctors informed about new tests, technologies, and advancements.
Distribute case studies and success stories to illustrate the real-world impact of genetic testing on patient outcomes.
Implement user-friendly electronic ordering and reporting systems that integrate seamlessly with existing Electronic Health Records (EHR) systems.
Simplify the test ordering process with clear instructions, easy-to-use forms, and efficient sample collection kits.
Establish a feedback mechanism to gather input from doctors on their experiences and suggestions for improvement.
Offer genetic counseling services to assist doctors in explaining test results to patients and planning subsequent steps.
Provide access to experienced genetic counselors for patient consultations.
Conduct clinical case reviews with doctors to discuss complex cases and determine the best testing strategies.
Collaborate on developing personalized patient care plans based on genetic test results.
Guarantee high-quality, accurate, and timely test results to build trust and reliability with doctors.
Adhere to strict quality control measures and continuously improve lab processes.
Provide clear and comprehensive test reports with actionable insights.
Ensure reports are easy to interpret and include recommendations for follow-up care.
We handle the complete billing process, from insurance claims submission to payment collection.
We ensure compliance with insurance regulations to avoid claim denials and delays.
Transparent pricing structure for genetic tests to avoid unexpected costs for patients and providers.
We act as a liaison between doctors, patients, and insurance companies to resolve billing issues and ensure timely reimbursements.
CASE STUDY