Question 1

What is Predictiv Care?

Accepted Answer

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.

Question 2

Is Predictiv Care a diagnostic service?

Accepted Answer

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.

Question 3

What type of samples does Predictiv Care use?

Accepted Answer

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.

Question 4

How accurate are the results?

Accepted Answer

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.

Question 5

What kind of insights do users receive?

Accepted Answer

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.

Question 6

Is my data secure?

Accepted Answer

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.

Question 7

Will my data be shared with third parties?

Accepted Answer

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.

Question 8

Can I use PredictivCare results with my doctor?

Accepted Answer

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

Question 9

Can results change over time?

Accepted Answer

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

Question 10

Why do we need to sequence all 20,000 genes?

Accepted Answer

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.

Question 11

What makes Predictiv Care different from other genetic testing companies?

Accepted Answer

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.

Question 12

Can businesses or partners work with Predictiv Care?

Accepted Answer

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.

Question 13

How do I get started?

Accepted Answer

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

Question 14

What is next generation sequencing?

Accepted Answer

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.

FAQs

Frequently asked questions