Create custom online forms that enable HIPAA compliance to securely collect the clinical trial data you need. Share your medical forms with participants to fill out on any device. Easy to customize with no coding required.
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Choose from ready-made form templates to get a head start on your electronic data capture system. Customize in seconds with our drag-and-drop builder.
Voordelen
Conduct clinical trials with ease using Jotform’s HIPAA-friendly online forms. Let participants fill out your clinical trial forms on any computer, tablet, or smartphone.
Share your HIPAA-friendly forms to seamlessly gather data from any device. All responses are protected with a 256-bit SSL connection and form encryption.
View responses in a spreadsheet, a calendar, or easy-to-read cards with Jotform Tables. You can also generate reports, collaborate with teammates, and assign prefilled forms for faster data collection.
With Jotform, your company has all the tools it needs to create professional, HIPAA-friendly forms. Get a signed Business Associate Agreement (BAA) and ensure your data is protected today.
Not only will you eliminate paper with online forms, but you can also use Jotform Workflows to build an approval flow that automatically sends emails, requests signatures, and more to speed up your workflow.
Drag and drop to create a clinical trial form, medical case report form, or other medical forms without coding. Add your logo, change fonts and colors, and update questions in a few easy clicks.
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eCRF software — or electronic case report form software — is used to collect and manage data about clinical studies and their participants. It’s a secure way to gather medical forms online, eliminating the need for messy paper forms.
Any organization that conducts clinical trials and issues electronic case report forms to participants could benefit from eCRF software.
Not only does an eCRF system keep your data organized, but it also helps you gather it efficiently and generate reports, improving your overall workflow.
Clinical data management is the collection and management of research data in a secure manner that aligns with the regulatory standards of the place where the clinical trial is being conducted.
An electronic data capture (EDC) system stores patient data that’s collected during clinical trials. It’s important to have a secure EDC system to keep medical data protected.