Generate clinical trial documents directly from your protocol
Clinials helps research sites and CROs turn complex trial protocols into clear, compliant documents and recruitment materials - in minutes, not weeks
No Credit Card Required
From Protocol to Content
Patient Information Sheet (P.I.S)
A patient-facing explanation of study objectives, risks, and participation details.
Operational Protocol Synopsis
A streamlined summary of key protocol objectives, design, endpoints, and operational details.
Budget Discovery
A list of activities, biomarkers and endpoints extracted from the protocol
Built for Compliance. Trusted for Security
Clinials uses study protocols only to generate trial documents. We do not recruit patients or access clinical databases.
Encrypted & Private
Documents never leave your organization
Compliant
GDPR, HIPAA ready
Controlled Access
Role-based permissions for sites, CROs, and sponsors
Versioning Control
Track and manage every draft with confidence
Loved by Clinical Teams
What users are saying,
“I have used Clinials on 3 studies now. The output is clean and very professional. I continually watch for updates as each one offers even more valuable features.
It allows our team to focus on other details knowing that these documents can be created seamlessly and quickly.”- Consultant for the medical research industry (USA)
“Super engaging and excellent platform.”
- CRA (USA)
“Where has this solution been? I’ve needed it forever. It’s amazing!”
- Site network Manager (USA)
“You have a great product that will only become increasingly powerful with continuous advancements in AI capabilities. I have a number of biotech clients and will discuss your solution with them.”
-Biotech advisor/consultant (Australia)
Built for Compliance. Trusted for Security
Clinials uses study protocols only to generate trial documents. We do not recruit patients or access clinical databases.
Encrypted & Private
Documents never leave your organization
Compliant
GDPR, HIPAA ready
Controlled Access
Role-based permissions for sites, CROs, and sponsors
Versioning Control
Track and manage every draft with confidence
Loved by Clinical Teams
What users are saying,
“I have used Clinials on 3 studies now. The output is clean and very professional. I continually watch for updates as each one offers even more valuable features.
It allows our team to focus on other details knowing that these documents can be created seamlessly and quickly.”- Consultant for the medical research industry (USA)
“Super engaging and excellent platform.”
- CRA (USA)
“Where has this solution been? I’ve needed it forever. It’s amazing!”
- Site network Manager (USA)
“You have a great product that will only become increasingly powerful with continuous advancements in AI capabilities. I have a number of biotech clients and will discuss your solution with them.”
-Biotech advisor/consultant (Australia)
Generate clinical trial documents directly from your protocol
Clinials turns complex trial protocols into clear, compliant documents in minutes!
No Credit Card Required
From Protocol to Content
Patient Information Sheet (P.I.S)
A patient-facing explanation of study objectives, risks, and participation details.
Operational Protocol Synopsis
A streamlined summary of key protocol objectives, design, endpoints, and operational details.
Patient Information Sheet (P.I.S)
A patient-facing explanation of study objectives, risks, and participation details.
How it Works
Step 1: Upload Protocol
Uploads are encrypted and private.
Step 2: Create Content
Generate operational reports and patient-facing content in multiple languages in minutes!
Step 3: Communicate your Trial
Manage your content! This includes:
Edit and Previewing
Versioning Control
Download in PDF, DOCX and CSV
Generate clinical trial documents directly from your protocol
Clinials helps research sites and CROs turn complex trial protocols into clear, compliant documents and recruitment materials - in minutes, not weeks
No Credit Card Required
Loved by Clinical Teams
What users are saying
“I have used Clinials on 3 studies now. The output is clean and very professional. I continually watch for updates as each one offers even more valuable features.
It allows our team to focus on other details knowing that these documents can be created seamlessly and quickly.”- Consultant for the medical research industry (USA)
“Super engaging and excellent platform.”
- CRA (USA)
“Where has this solution been? I’ve needed it forever. It’s amazing!”
- Site network Manager (USA)
“I think you have a great product that will only become increasingly powerful with continuous advancements in AI capabilities.
I have a number of biotech clients and will discuss your solution with them.”- Biotech advisor/consultant (Australia)
Built for Compliance. Trusted for Security
Clinials uses study protocols only to generate trial documents. We do not recruit patients or access clinical databases.
Encrypted & Private
Documents never leave your organization
Compliant
GDPR, HIPAA ready
Controlled Access
Role-based permissions for sites, CROs, and sponsors
Versioning Control
Track and manage every draft with confidence
Loved by Clinical Teams
What users are saying,
“I have used Clinials on 3 studies now. The output is clean and very professional. I continually watch for updates as each one offers even more valuable features.
It allows our team to focus on other details knowing that these documents can be created seamlessly and quickly.”- Consultant for the medical research industry (USA)
“Super engaging and excellent platform.”
- CRA (USA)
“Where has this solution been? I’ve needed it forever. It’s amazing!”
- Site network Manager (USA)
“You have a great product that will only become increasingly powerful with continuous advancements in AI capabilities. I have a number of biotech clients and will discuss your solution with them.”
-Biotech advisor/consultant (Australia)
How it Works
Step 1: Upload Protocol
Uploads are encrypted and private.
Step 2: Create Content
Generate operational reports and patient-facing content in multiple languages in minutes!
Step 3: Communicate your Trial
Manage your content! This includes:
Edit and Previewing
Versioning Control
Download in PDF, DOCX and CSV
How it Works
Step 1: Upload Protocol
Uploads are encrypted and private.
Step 2: Create Content
Generate operational reports and patient-facing content in multiple languages in minutes!
Step 3: Communicate your Trial
Manage your content! This includes:
Edit and Previewing
Versioning Control
Download in PDF, DOCX and CSV
Ready to experience the difference?
Built for Compliance. Trusted for Security
Clinials uses study protocols only to generate trial documents. We do not recruit patients or access clinical databases.
Encrypted & Private
Documents never leave your organization
Compliant
GDPR, HIPAA ready
Controlled Access
Role-based permissions for sites, CROs, and sponsors
Versioning Control
Track and manage every draft with confidence
Loved by Clinical Teams
What users are saying,
“I have used Clinials on 3 studies now. The output is clean and very professional. I continually watch for updates as each one offers even more valuable features.
It allows our team to focus on other details knowing that these documents can be created seamlessly and quickly.”- Consultant for the medical research industry (USA)
“Super engaging and excellent platform.”
- CRA (USA)
“Where has this solution been? I’ve needed it forever. It’s amazing!”
- Site network Manager (USA)
“You have a great product that will only become increasingly powerful with continuous advancements in AI capabilities. I have a number of biotech clients and will discuss your solution with them.”
-Biotech advisor/consultant (Australia)
How it Works
Step 1: Upload Protocol
Uploads are encrypted and private.
Step 2: Create Content
Generate operational reports and patient-facing content in multiple languages in minutes!
Step 3: Communicate your Trial
Manage your content! This includes:
Edit and Previewing
Versioning Control
Download in PDF, DOCX and CSV
Ready to experience the difference?
Ready to experience the difference?
Built for Compliance. Trusted for Security
Clinials uses study protocols only to generate trial documents.
We do not recruit patients or access clinical databases.
Encrypted & Private
Documents never leave your organization
Compliant
GDPR, HIPAA ready
Controlled Access
Role-based permissions for sites, CROs, and sponsors
Versioning Control
Track and manage every draft with confidence
Encrypted & Private
Documents never leave your organization
Compliant
GDPR, HIPAA ready
Controlled Access
Role-based permissions for sites, CROs, and sponsors
Versioning Control
Track and manage every draft with confidence
From Protocol to Content
Patient Information Sheet (P.I.S)
A patient-facing explanation of study objectives, risks, and participation details.
Operational Protocol Synopsis
A streamlined summary of key protocol objectives, design, endpoints, and operational details.
Budget Discovery
A list of activities, biomarkers and endpoints extracted from the protocol