For Biotech Sponsors

For biotech sponsors that need real-world evidence.

BeaconCR helps early-stage and growth-stage biotechnology companies develop registry-based evidence strategies, activate physician sites, organize observational data collection, and build structured real-world evidence programs around investigational or commercially available products, as appropriate.

Product tracking

For sponsor programs involving biologics, devices, cell therapies, or combination products, BeaconCR provides product-tracking workflows that link patient outcomes back to product lot, dose, device serial, or shipment.

BeaconCR integrates with the BioTrace blockchain chain-of-custody system on partner platforms when full traceability is needed.

Clinical trial awareness & recruitment

BeaconCR builds patient-education materials, physician landing pages, and clinical-trial awareness campaigns for sponsor programs that need to reach the right physicians and patients without making improper therapeutic claims.

Recruitment content is reviewed for compliance with IRB-approved language and the sponsor's regulatory posture.

Sponsor application patterns

Anonymized illustrative examples of how biotech sponsors apply BeaconCR for real-world evidence and registry programs.

Orthobiologic

Orthobiologic Registry

A regenerative-medicine clinic capturing knee outcomes from PRP and bone-marrow-aspirate injections across multi-year follow-up — without building research infrastructure in-house.

Intranasal CNS

Intranasal CNS Pathway

An expanded-access pathway for intranasal neurological therapy — compassionate-use intake, site activation, and observational data capture as a precursor to a larger sponsor-led program.

Cell Therapy

Cell Therapy Traceability Registry

A cell-therapy registry tying outcomes to product lots across multiple physician sites administering an investigational autologous cell preparation, with chain-of-custody traceability end-to-end.

Functional Medicine

Functional Medicine Registry

A functional-medicine clinic turning a structured multi-component protocol into evidence — longitudinal outcomes and labs in a registry framework supporting eventual publication.

Sponsor RWE

Sponsor RWE Program

A growth-stage biotech building a real-world evidence program around physician-prescribed use — outcomes across activated sites, evidence packages for investors, partners, and future regulatory planning.

Compassionate Use

Compassionate Use Pathway

A physician-led pathway for patients seeking access to investigational, regenerative, biologic, or device-enabled therapy — structured intake, documentation support, consent routing, and longitudinal outcomes tracking.

Use case patterns above are illustrative and anonymized. BeaconCR does not publish identifiable case studies without explicit sponsor, physician, and (where applicable) patient consent. Observational registry data is hypothesis-generating and is not equivalent to RCT data.

Sponsor data reports

Periodic sponsor-facing reports include enrolled-patient counts, follow-up rates, outcome trends, safety observations, and registry-level summaries. Reports clearly distinguish observational data from RCT data.

Build a Sponsor Registry Program