INDUSTRY LEADERS RELY ON APRYSE
Pharma & Life Science Document Processing Use Cases
How pharmaceutical and life science organizations leverage document processing SDKs
Clinical Trial Complexity
Using inconsistent file formats in clinical trial workflows complicates data accuracy and reporting efforts. Standardize clinical trial documentation by converting any file to the right format, simplifying patient data sharing across EHR systems, labs, and PHRs while recording every file interaction and submission.
Document Manipulation Features
SOC2
Apryse prioritizes security compliance as critical requirement and necessary investment to support the rigorous data requirements of our pharmaceutical customers. Our information security practices, policies, procedures, and operations meet the SOC 2 standards for security. Additionally, we also have products which have obtained ISO 27001:2017 certification of its Information Security Management Systems (ISMS).
Document Security Features
The Most Complete Suite of Document Processing SDKs on the Market
Our SDKs, pre-built components and end-user SaaS applications enable the world’s leading pharma and life science companies to easily generate, convert, view, edit, and sign documents within their applications and workflows.
Loved by Developers
Apryse offers easy-to-deploy developer tools for server, mobile, and client-side document processing. These tools enable developers to push forward strategic initiatives, such as process automation and digital self-service, while also adhering to regulatory standards.
Accelerate projects with our team of experienced SDK developers. We offer support through your unlimited trial to the finish line, and beyond.
Eliminate potential vulnerabilities. No outside dependencies mean you can deploy on your infrastructure without data ever leaving your platform.
Be ready for what comes next. Adapt your product at the speed of user needs with Apryse’s full-featured developer suite that scales with you.
