For Sponsors

For Sponsors

For Sponsors

Fixed-fee,
audit-ready
RWD in weeks

Fixed-fee, audit ready RWD in weeks

Fixed-fee, audit-ready RWD in weeks

Set up multimodal registries and non-interventional studies, gather precision data, and engage a vibrant community of patients—delivered faster, at a fraction of CRO costs.

Set up multimodal registries and non-interventional studies, gather precision data, and engage a vibrant community of patients—delivered faster, at a fraction of CRO costs.

Set up multimodal registries and non-interventional studies, gather precision data, and engage a vibrant community of patients—delivered faster, at a fraction of CRO costs.

Request a demo

Request a demo

Request a demo

Pharmaceutical corporate employee smiling in an office with other coworkers in the background
A view of Embleema's sponsor dashboard with charts and graphs
Pharmaceutical corporate employee smiling in an office with other coworkers in the background
A view of Embleema's sponsor dashboard with charts and graphs
Pharmaceutical corporate employee smiling in an office with other coworkers in the background
A view of Embleema's sponsor dashboard with charts and graphs

<1%

<1%

year over year patient drop-off

60,000+

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

1/3

1/3

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

Disease-specific data for precision medicine 

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

Launch siteless or hybrid studies in weeks, not months.

Skip long CRO timelines and custom builds. We set up your study using our customizable workflows and prebuilt templates to help you launch complex studies fast, staying audit-ready from day one.

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

Launch siteless or hybrid studies in weeks, not months.

Skip long CRO timelines and custom builds. We set up your study using our customizable workflows and prebuilt templates to help you launch complex studies fast, staying audit-ready from day one.

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

Launch siteless or hybrid studies in weeks, not months.

Skip long CRO timelines and custom builds. We set up your study using our customizable workflows and prebuilt templates to help you launch complex studies fast, staying audit-ready from day one.

Then, multimodal data linked at the patient-level continuously flows into your study database

EHRs, labs, wearables, site generated and patient-reported data often live in silos. Our platform natively integrates multimodal structured and unstructured data into a unified patient-level record.

Data is quality-controlled, normalized and appended in real-time in the study database.

Then, multimodal data linked at the patient-level continuously flows into your study database

EHRs, labs, wearables, site generated and patient-reported data often live in silos. Our platform natively integrates multimodal structured and unstructured data into a unified patient-level record.

Data is quality-controlled, normalized and appended in real-time in the study database.

Then, multimodal data linked at the patient-level continuously flows into your study database

EHRs, labs, wearables, site generated and patient-reported data often live in silos. Our platform natively integrates multimodal structured and unstructured data into a unified patient-level record.

Data is quality-controlled, normalized and appended in real-time in the study database.

Next, build a long-term dynamic patient community available for studies

Access a fully consented patient community with shared records and strong patient-reported outcomes response rates. We identify eligible patients, manage consent, and sustain follow-up—fueling richer datasets.

Next, build a long-term dynamic patient community available for studies

Access a fully consented patient community with shared records and strong patient-reported outcomes response rates. We identify eligible patients, manage consent, and sustain follow-up—fueling richer datasets.

Next, build a long-term dynamic patient community available for studies

Access a fully consented patient community with shared records and strong patient-reported outcomes response rates. We identify eligible patients, manage consent, and sustain follow-up—fueling richer datasets.

Result: rich, on-demand, patient-level insights.

Access your real-time multimodal dataset anytime, with no data cuts required, and analyze it using the same advanced tools the FDA uses for regulatory reviews.

Result: rich, on-demand, patient-level insights.

Access your real-time multimodal dataset anytime, with no data cuts required, and analyze it using the same advanced tools the FDA uses for regulatory reviews.

Result: rich, on-demand, patient-level insights.

Access your real-time multimodal dataset anytime, with no data cuts required, and analyze it using the same advanced tools the FDA uses for regulatory reviews.

Trusted by industry leaders

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

Coworkers at a desk on computers working

“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

Real-world studies we power

Drug-Effectiveness

Drug Safety Monitoring

Natural History

HEOR & Cost‑Effectiveness

Comparative Effectiveness

Ad Hoc Exploratory Research

Prospective Studies

Coworkers at a desk on computers working

“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

Real-world studies we power

Drug-Effectiveness

Drug Safety Monitoring

Natural History

HEOR & Cost‑Effectiveness

Comparative Effectiveness

Ad Hoc Exploratory Research

Prospective Studies

Coworkers at a desk on computers working

“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

Real-world studies we power

Drug-Effectiveness

Drug Safety Monitoring

Natural History

HEOR & Cost‑Effectiveness

Comparative Effectiveness

Ad Hoc Exploratory Research

Prospective Studies

Why sponsors choose Embleema

Trusted by leaders across rare disease, neurology, and autoimmune diseases

An icon of a phone with medical symbols
An icon of a phone with medical symbols
An icon of a phone with medical symbols
Patients as partners

Our patient app returns data to patients and delivers personalized services to enhance engagement and adherence.

An icon of an hourglass
An icon of an hourglass
An icon of an hourglass
Site accelerators

Investigators and site staff minimize time navigating through disparate, counter-intuitive tools, focusing instead on participants and research.

An icon of DNA
An icon of DNA
An icon of DNA
Designed for precision medicine

Our platform is the sole one used by the FDA for its bioinformatics analysis of cell and gene therapies regulatory approvals.

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Case studies

A patient and a doctor sitting in an office having a conversation
A patient and a doctor sitting in an office having a conversation
A patient and a doctor sitting in an office having a conversation
Improving Epilepsy Drug Development through Real-World Data and Patient Communities

Read more

Read more

Read more

Two medical professionals looking at a tablet
Two medical professionals looking at a tablet
Two medical professionals looking at a tablet
How a Patient-First Epilepsy Registry Delivers Real-World Evidence in Months, Not Years

Read more

Read more

Read more

A doctor going over medical information with a patient
A doctor going over medical information with a patient
A doctor going over medical information with a patient
How Eisai Gained Patient-Level RWE on Seizure Outcomes in 3 Months

Read more

Read more

Read more

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An icon of paper with words
An icon of paper with words

Read our scientific publications

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

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Break the bottlenecks in real-world research

See how Embleema gives you the speed, control, and compliance to run real-world research on your terms.

Request a demo

Request a demo

Request a demo