For Sponsors

Launch complex studies in days at a fraction of the cost

Our customizable workflows and prebuilt templates replace long CRO timelines and custom builds, helping you stay audit-ready from day one.

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<1%

year over year patient drop-off

60,000+

care centers connected flowing in data from EMRs across the U.S.

1/3

cost of study build and time to first patient visit vs CRO

Flexible solutions that scale with you

Meet changing study needs without cumbersome implementations or the addition of new technology vendors.

Rapidly set up your study

Launch siteless or hybrid studies in weeks with customizable workflows, cutting costs by 30 to 50% and avoiding vendor overages.

Integrate complex data capture

Capture complex, multimodal data from sites, patients, labs, and 60,000+ care centers, unified and audit‑ready from day one to enrich your registry.

Leverage analytics & bioinformatics

Normalize, enrich, and analyze data with our AI-powered platform designed for complex modalities and longitudinal datasets.

Recruit engaged patients

Stay connected with our vibrant patient communities to gather ongoing, fully consented follow‑up insights—enabling future research opportunities.

Disease-specific data for precision medicine

First, we build your study with our no-code EDC platform

Define your protocol, send us your requirements, and we will build it in a matter of days.

First, we build your study with our no-code EDC platform

Define your protocol, send us your requirements, and we will build it in a matter of days.

Then, streamline quality control for faster FDA submissions

Generate compliant study data using required vocabularies and data dictionaries
Live quality controls surface issues and prevent unnecessary site queries
Data follows FDA, CDISC, CDASH, and FAIR guidelines for regulatory compliance
Automated PII-stripping maintains patient privacy compliance

Then, streamline quality control for faster FDA submissions

Generate compliant study data using required vocabularies and data dictionaries
Live quality controls surface issues and prevent unnecessary site queries
Data follows FDA, CDISC, CDASH, and FAIR guidelines for regulatory compliance
Automated PII-stripping maintains patient privacy compliance

Pull patient data, digitize documents, validate automatically

Electronic Medical Record (EMR) integration pre-fills data to reduce entry time and errors
Drag-and-drop converts PDFs to eCRFs with full traceability
Real-time edit checks catch missing or incorrect values
Custom fields handle complex, disease-specific data
Single dashboard shows live data collection status

Pull patient data, digitize documents, validate automatically

Electronic Medical Record (EMR) integration pre-fills data to reduce entry time and errors
Drag-and-drop converts PDFs to eCRFs with full traceability
Real-time edit checks catch missing or incorrect values
Custom fields handle complex, disease-specific data
Single dashboard shows live data collection status

All multimodal data unified and updated in real time

Aggregate data from EHRs, labs, wearables, site-generated, and patient-reported sources
Standardize and quality-check both structured and unstructured data instantly

All multimodal data unified and updated in real time

Aggregate data from EHRs, labs, wearables, site-generated, and patient-reported sources
Standardize and quality-check both structured and unstructured data instantly

Speed your enrollment with our dynamic patient community

Tap into a fully consented patient community with shared records and high patient-reported outcome response rates
We identify eligible patients, manage consent, and sustain ongoing follow‑up

Speed your enrollment with our dynamic patient community

Tap into a fully consented patient community with shared records and high patient-reported outcome response rates
We identify eligible patients, manage consent, and sustain ongoing follow‑up

Trusted by industry leaders

“The team at Embleema demonstrates extensive and deep domain knowledge as well as provided strategic support for preclinical and regulatory activities. We plan to work with them again in the future.”

Daniel D.

CEO Biotech

Daniel D.

CEO Biotech

A person holding a smartphone with a screen to the Embleema patient app to record symptoms

On demand data without delays.

Your study data is updated in real time, letting sponsors bypass expensive and unnecessary data cuts.

Request a demo

A notification of a patient who uploaded an MRI 10 minutes ago

A screenshot of a medication list of the Embleema platform

A notification of a patient who recorded a seizure 1 hour ago

A notification of a patient with a new sequencing file in their records that came 30 minutes ago

Supporting sponsors, sites, and patients

Simple

Detailed

Embleema

Typical CRO

Pricing model

Low fixed fee

Variable custom pricing

Speed to launch

Less than 6 weeks

6-months+

Patients, sites and investigators

Integrated software suite

Patchwork of third party tools

Platform adaptability

High, configuration-based

Low, additional dev and SOWs

Multimodal data

Natively unified at patient-level

Sitting in fragmented systems

Dedicated support

Multi-channel support for proactive resolution

Call-center with longer wait times

Simple

Detailed

Embleema

Typical CRO

Pricing model

Low fixed fee

Variable custom pricing

Speed to launch

Less than 6 weeks

6-months+

Patients, sites and investigators

Integrated software suite

Patchwork of third party tools

Platform adaptability

High, configuration-based

Low, additional dev and SOWs

Multimodal data

Natively unified at patient-level

Sitting in fragmented systems

Dedicated support

Multi-channel support for proactive resolution

Call-center with longer wait times

Simple

Detailed

Embleema

Typical CRO

Pricing model

Low fixed fee

Variable custom pricing

Speed to launch

Less than 6 weeks

6-months+

Patients, sites and investigators

Integrated software suite

Patchwork of third party tools

Platform adaptability

High, configuration-based

Low, additional dev and SOWs

Multimodal data

Natively unified at patient-level

Sitting in fragmented systems

Dedicated support

Multi-channel support for proactive resolution

Call-center with longer wait times

Request a demo

Case studies

A patient and a doctor sitting in an office having a conversation

Improving Epilepsy Drug Development through Real-World Data and Patient Communities

Two medical professionals looking at a tablet

How a Patient-First Epilepsy Registry Delivers Real-World Evidence in Months, Not Years

A doctor going over medical information with a patient

How Eisai Gained Patient-Level RWE on Seizure Outcomes in 3 Months

Real-world studies we power

Drug-Effectiveness

Drug Safety Monitoring

Natural History

HEOR & Cost‑Effectiveness

Comparative Effectiveness

Ad Hoc Exploratory Research

Prospective Studies

Read our scientific publications

100+ submissions supported to date, from gene therapies to RWE

Say goodbye to silos and delays

See how Embleema unifies study design, data capture, patient engagement, and analytics—with live data from setup to submission, no delays or manual refreshes.

Request a demo

Say goodbye to silos and delays

See how Embleema unifies study design, data capture, patient engagement, and analytics—with live data from setup to submission, no delays or manual refreshes.

Request a demo

Say goodbye to silos and delays

See how Embleema unifies study design, data capture, patient engagement, and analytics—with live data from setup to submission, no delays or manual refreshes.

Request a demo

Launch complexstudies in days at a fraction of the cost

Launch complexstudies in days at a fraction of the cost

Launch complex studies in days at a fraction of the cost

<1%

<1%

60,000+

1/3

1/3

Flexible solutions that scale with you

Rapidly set up your study

Integrate complex data capture

Leverage analytics & bioinformatics

Recruit engaged patients

Disease-specific data for precision medicine

First, we build your study with our no-code EDC platform

First, we build your study with our no-code EDC platform

First, we build your study with our no-code EDC platform

Then, streamline quality control for faster FDA submissions

Then, streamline quality control for faster FDA submissions

Then, streamline quality control for faster FDA submissions

Pull patient data, digitize documents, validate automatically

Pull patient data, digitize documents, validate automatically

Pull patient data, digitize documents, validate automatically

All multimodal data unified and updated in real time

All multimodal data unified and updated in real time

All multimodal data unified and updated in real time

Speed your enrollment with our dynamic patient community

Speed your enrollment with our dynamic patient community

Speed your enrollment with our dynamic patient community

On demand data without delays.

Supporting sponsors, sites, and patients

Embleema

Typical CRO

Embleema

Typical CRO

Embleema

Typical CRO

Case studies

Improving Epilepsy Drug Development through Real-World Data and Patient Communities

How a Patient-First Epilepsy Registry Delivers Real-World Evidence in Months, Not Years

How Eisai Gained Patient-Level RWE on Seizure Outcomes in 3 Months

Real-world studies we power

Read our scientific publications

Say goodbye to silos and delays

Say goodbye to silos and delays

Say goodbye to silos and delays

Launch complex
studies in days at a
fraction of the cost

Launch complex
studies in days at a
fraction of the cost