Adobe PDF Library SDK
Global OEMs, SaaS and enterprise end-users rely on Adobe PDF Library to automate the creation, editing and management of PDFs. An Adobe partner, our SDK uses the same source code as Acrobat for stability, reliability and quality results.
Languages: .NET, .NET Framework, Java and C/C++
Platforms: Windows, Linux & MacOS
Package managers: NuGet & Maven
Capabilities include but are not limited to:
-Annotations
-Content creation
-Content modification
-Color management
-Extraction - text, images, forms
-Compression/optimize
-Conversion - PDF/A, PDF/X, EPS, PostScript, XPS, ZUGFeRD, color
-Display, Printing
-Extract text, images & other content
-Forms - Import, export, flatten static & dynamic XFA forms, AcroForms
-Images - extract, import/export, thumbnails, render/rasterize pages, separations
-Optimization - size, content, images, etc.
-OCR - add text to document, add text to image
-PDF to Office Documents (Word, Excel, PPT)
-Security - Viewer settings, redactions, password, encrypt/decryption, watermark
Pricing options for OEMs, SaaS & end-users are flexible and based on usage.
Shorten development times & get to market faster with Adobe PDF Library. Free trial - download today.
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Identity Matrix
Identity Matrix helps you increase revenue while spending less. The platform identifies 70% of US web visitors at a person-level. Set up page intent and lead scoring rules, then store them directly in your CRM for direct outreach.
With person-level attribution, market-leading contact information, and a full view of the customer journey, Identity Matrix helps you solve marketing's toughest questions:
1. Where is your best traffic coming from?
2. What does the customer journey look like - step by step?
3. How can I contact high-intent, in-market leads?
With upcoming GenAI features to help with customer journey analysis, conversion rate optimization suggestions and more, Identity Matrix is the data provider your competitors are switching to.
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Clinion CTMS
Most Easy-to-Use Clinical Trial Management System (CTMS)
𝐂𝐥𝐢𝐧𝐢𝐨𝐧 𝐂𝐓𝐌𝐒 integrates seamlessly with Clinion EDC and Clinion RTSM to provide detailed and faster access to the entire trial process to address all aspects of Clinical trial management from a single platform: investigator sites, patients enrollment, SAEs, deviations, inclusions, visit scheduling, IP management, milestones, finances, custom reports, and on-demand analytics enables you to improve quality, control risk, and reduce costs.
Clinion CTMS is modular in design
These modules are available:
Admin Module
Project Management
Site Monitoring Activities
Finance and Budget Management
Safety Reporting
Management of IP Inventory
Document Management System
Audit/Activity Log
Comprehensive dashboards
Comprehensive Reports
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Cenduit IRT
Modern Interactive Response Technology (IRT) systems are becoming more intricate. The significance of flexible and customizable IRT cannot be overstated, as this technology serves as the primary source for essential data, including recruitment metrics, clinical trial attrition rates, patient attendance, and more. It is vital to select a platform that is intuitive, optimized for mobile use, and all-encompassing—underpinned by high standards of quality, adaptability, and expertise. Embrace a partnership that offers profound therapeutic knowledge tailored to the contemporary risk-based eClinical landscape. By merging advanced technology with specialized knowledge and a dedication to exceptional service, we enhance clinical trials to achieve favorable patient results. Our extensive understanding of clinical processes and supply chain dynamics fosters innovation, granting clients greater control over their Randomization and Trial Supply Management (RTSM) protocols. Our cutting-edge tools elevate quality assurance, improve site productivity, and enhance patient adherence significantly. Furthermore, our IRT platform is adaptable enough to cater to a wide array of studies, with the capability for full validation and deployment in just 30 days, ensuring efficiency in clinical trial operations. This swift implementation can lead to more timely data collection and improved overall trial management.
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