Predictiv Care is a precision health platform that integrates genomic data with advanced analytics to generate personalized health insights. Our focus is on risk assessment, drug response insights, and wellness-related traits, delivered through a secure digital platform.

No. PredictivCare does not provide medical diagnoses or treatment decisions. Our reports are intended to support informed discussions with healthcare professionals and to improve personal understanding of health-related risks and responses.

This distinction matters legally and clinically and we don’t blur it.

Depending on the program, PredictivCare can work with non-invasive or minimally invasive biological samples (such as blood or other approved sample types), processed using next-generation sequencing (NGS) technologies.

Exact sample requirements vary by offering and partner program.

The underlying sequencing data meets industry standards for quality control. However, genetics is only one component of health. Environment, lifestyle, and clinical context play major roles.

Anyone claiming “certainty” from genomics alone is overselling.

Reports may include:

• Genetic risk indicators for select health conditions

• Pharmacogenomic insights related to drug metabolism and response

• Wellness-associated traits (e.g., metabolism, endurance, nutritional tendencies)

Importantly: insights are probabilistic, not deterministic.

Yes. Data security and privacy are core priorities. Predictiv Care uses:

• Encrypted data storage

• Controlled access systems

• Compliance-aligned data handling practices

We do not sell personal genetic data.

You can read further in our Private Policy and Terms.

Data is shared only with explicit consent or as required to deliver the service (e.g., certified labs, approved partners). Users retain control over their data permissions.

No hidden data monetization models.

You can read further in our Private Policy and Terms.

Yes and that’s encouraged. Our reports are designed to be interpretable by healthcare professionals, supporting more informed conversations rather than replacing clinical judgment.

Yes. As scientific knowledge evolves and models are refined, interpretations may be updated. Genetics doesn’t change but our understanding of it does.

To be proactive!

The DNA sequence of 20,000 genes is like the blueprint for a building. If you see a problem in a building structure, you may want to see the blueprint to identify the problem. The best approach is to prevent a problem even before it happens if you can find its origins in the blueprint. Sequencing all 20,000 genes is like having a complete blueprint for all of your genes.

Another benefit for sequencing all 20,000 genes is that you can quickly evaluate your genetic susceptibilities to conditions that you would not consider now. From our Standard Package, we provide easy electronic access to all your variants of your genes.

Predictiv Care emphasizes:

• Responsible interpretation over sensational claims

• Integration of genomics with analytics, not just raw reports

• Flexible deployment across research, wellness, and healthcare settings

We are building infrastructure, not novelty reports.

Yes. We collaborate with organizations across healthcare, wellness, and research to pilot and deploy precision health solutions.

Partnerships are structured, not one-size-fits-all.

You can explore available offerings directly through our website or contact us to discuss individual or organizational use cases.

We use a DNA sequencer based on next generation sequencing technology. Compared to other DNA sequencing technologies, it allows high through put sequencing possible by the massively parallel sequencing feature.