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Celegence
What AI says about Celegence
Celegence specializes in regulatory services for the Pharmaceutical, Medical Device, and In-Vitro Diagnostics industries. By leveraging AI technology, they enhance compliance, speed, and accuracy in regulatory documentation and submissions.
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Products & Services
AI-Empowered Regulatory Services
Comprehensive regulatory services including regulatory publishing, eCTD submissions, and consulting for pharmaceutical and medical device manufacturers.
CAPTIS® AI Platform
An in-house AI-powered technology designed to streamline medical writing and documentation processes.
Dossplorer™
A cloud eCTD viewer and manager for regulatory document management.
Common Questions
What industries does Celegence serve?
Celegence serves the Pharmaceutical, Medical Device, and In-Vitro Diagnostics industries.
What is the CAPTIS® AI Platform?
The CAPTIS® AI Platform is an in-house AI-powered technology that streamlines medical writing and documentation processes.
What types of regulatory services does Celegence offer?
Celegence offers services such as regulatory publishing, eCTD submissions, technical writing, and regulatory affairs consulting.
How does Celegence ensure compliance?
Celegence leverages AI technology to enhance regulatory accuracy and reduce compliance burdens for their clients.
Where is Celegence located?
Celegence is headquartered in Chicago, IL, USA.