For Sponsors

For Sponsors

For Sponsors

Launch complex
studies in days at a
fraction of the cost

Fixed-fee, audit ready RWD in weeks

Fixed-fee, audit-ready RWD in weeks

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

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

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

Request a demo

Request a demo

Request a demo

Higher patient completion

We treat our patients as partners with personalized services to enhance engagement and adherence.

Site accelerators

Sites minimize time navigating multiple systems, focusing instead on participants and research.

FDA standards

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

Disease-specific data for precision medicine 

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

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

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

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

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

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

Streamline quality control for faster FDA submissions

Streamline quality control for faster FDA submissions

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.

Pull patient data, digitize documents, validate automatically.

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

All multimodal data unified and updated in real time

All multimodal data unified and updated in real time

EHRs, labs, wearables, site-generated, and patient-reported data in one platform. Structured and unstructured data are quality-controlled and normalized.

EHRs, labs, wearables, site-generated, and patient-reported data in one platform. Structured and unstructured data are quality-controlled and normalized.

EHRs, labs, wearables, site-generated, and patient-reported data in one platform. Structured and unstructured data are quality-controlled and normalized.

Speed your enrollment with our dynamic patient community

Speed your enrollment with our dynamic patient community

Speed your enrollment with our dynamic patient community

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.

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.

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.

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

“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

“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

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

Real-world studies we power

Drug-Effectiveness

Drug Safety Monitoring

Natural History

HEOR & Cost‑Effectiveness

Comparative Effectiveness

Ad Hoc Exploratory Research

Prospective Studies

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

Read our scientific publications

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

See more

See more

See more

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