Most of modern medicine is designed to answer a population-level question: What is safe and effective for millions of people? Radence is different. We determine what is best for you, based on everything we know today.
By the time a clinical guideline is published and implemented, the underlying evidence may already be five to ten years old. Medical committees move slowly because they must balance safety, liability, cost, and applicability across broad populations.
We apply evidence to individuals before guidelines catch up.
Our members undergo comprehensive cardiovascular, metabolic, genomic, imaging, and cancer screening assessments that generate a far richer understanding of their individual risk than guideline committees typically consider. That additional information changes what we can act on.
The Radence Framework Behind Every Recommendation
Our recommendations are based on four inputs:
- Evidence quality: what the clinical literature, trials, and real-world data show today.
- Risk-benefit profile: the magnitude of potential upside relative to the likelihood and severity of harm.
- Expert alignment: how leading physicians and specialists interpret the evidence and where consensus is emerging.
- Member applicability: how well an intervention fits your biology, risk factors, goals, and willingness to adopt.
TechAtlas, RA Capital’s research group of PhDs and MDs, continuously evaluates these four inputs to develop individualized recommendations.
How We Evaluate Emerging Evidence
When evaluating new therapies, diagnostics, and preventive interventions, we start with the strongest available clinical data: large randomized controlled trials designed to determine whether an intervention truly causes a meaningful outcome.
We also evaluate:
- Analyses of group trials
- Prospective cohort studies that track defined groups over time
- Retrospective analyses of existing data
- Case series
- Mechanistic and preclinical research
Each type of evidence contributes differently to understanding benefit, risk, and biological plausibility. Most importantly, we do not review evidence on a fixed schedule.
New publications, conference presentations, and clinical trial results are continuously evaluated as they emerge. The objective is to understand what today’s evidence supports for a member with a specific risk profile.
We Use a Risk-Proportionate Threshold
The most important decision in any clinical framework is determining how much evidence is enough to act. Radence answers that question differently than guideline bodies do by applying a risk-proportionate threshold:
- Lower-risk interventions with meaningful potential upside may justify action earlier.
- Higher-risk interventions require substantially stronger evidence before they are recommended.
Consider three examples:
- A whole-body MRI carries no radiation exposure and relatively low risk, while potentially identifying disease before symptoms develop. Because the downside is relatively low, emerging evidence may be sufficient to support its use in appropriately selected individuals.
- While a DEXA scan has some low-level radiation exposure, it is not zero. The benefit in identifying bone density issues before a fracture occurs, however, could be clinically significant and worthwhile, particularly in individuals with risk factors for osteoporosis, such as sedentary lifestyles and nutritional deficiencies.
- Scans such as Coronary CT angiography (CCTA) carry additional considerations, including radiation exposure, intravenous contrast, and potentially medication to optimize physiological parameters for imaging quality requirements. It can, however, provide a detailed assessment of soft and calcified coronary plaque burden.
Applying the same evidentiary standard to all three scenarios would be a mistake. Precision medicine requires matching the strength of evidence to the risk of action.
Why Expert Judgment Matters
Published evidence is necessary but rarely sufficient on its own.
Leading physicians often identify meaningful shifts in a field before those shifts appear in formal guidelines. Their interpretation of emerging evidence, real-world experience, and understanding of downstream effects provide critical context.
This is where our research network becomes particularly valuable. We continuously evaluate emerging biomedical evidence and maintain relationships with leading experts across cardiology, neurology, oncology, endocrinology, and precision diagnostics.
When experts independently converge on the same interpretation of new evidence, confidence increases. When experts disagree, that disagreement itself becomes important information. Consensus among experts doesn’t replace evidence. It helps contextualize it.
Precision Medicine Requires a Different Standard
Traditional clinical guidelines are designed for populations. Radence is designed for individuals. When we have access to whole-genome sequencing, advanced imaging, metabolic and cardiovascular phenotyping, cancer screening, health data tracked over time, we can evaluate emerging therapies in the context of your unique biology rather than a population average.
This requires a more demanding standard of interpretation, not a lower one. The evidence must be strong enough to support an individualized decision, not just a population recommendation. The result is a standard of care that evolves at the pace of scientific discovery rather than waiting for consensus to catch up.


