Amissa supports research partnerships by providing secure access to de-identified patient data, only when patients have consented.
Steps
Submit a research inquiry.
Contact the Amissa research team through the Help Center.
Provide details about your study, including objectives, IRB approval status, and required data types.
Complete the review process.
The Amissa team will evaluate your request for feasibility, compliance, and alignment with platform standards.
You may be asked to provide supporting documents, such as your IRB approval letter or data management plan.
Sign a research agreement.
If your request is approved, you will receive a formal agreement covering scope of access, data handling requirements, and timelines.
Access the data.
Approved researchers will be granted secure access to de-identified, consented data sets.
Data is provided in a format that aligns with your approved study design.
Helpful Details
Only de-identified data is shared, and only from patients who have provided consent.
Amissa does not sell data to advertisers or marketers.
Researchers are responsible for complying with all applicable ethical and regulatory requirements.
Next Steps
If you are interested in collaborating, contact the Amissa research team to begin the request process [email protected].