WERX
Werx delivers powerful construction management tools at a price contractors love—starting at just $49/month. Built for small to midsized businesses, Werx simplifies your workflow with features like flexible estimating, AIA-Style billing, QuickBooks syncing, and labor tracking. Speed up payments with Stripe-powered online billing. Try Werx free for 30 days and see the difference!
Tailored for contractors of all trades, Werx helps you save time, reduce stress, and boost profits. From managing schedules to tracking time in the field and creating polished invoices, Werx brings everything together in one easy-to-use platform. Affordable, reliable, and built to help your business grow—Werx is the smart choice for contractors.
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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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OpenText Clinical Trial Quality Management
In recent years, the Life Sciences sector has incurred nearly $15 billion in fines and settlements related to compliance, underscoring the importance for firms to follow best practices in pharmaceuticals, medical devices, and biotechnology. Additionally, the way clinical trials are managed can greatly influence the timeline, scope, and financial resources allocated for the development of drugs or medical devices. Utilizing OpenText™ Clinical Trial Quality Management System (ctQMS) allows organizations to maintain compliance, lower record management expenses, and foster collaboration to implement best practices throughout the entire clinical trial lifecycle. This strategic approach not only enhances operational efficiency but also contributes to the overall success of product development initiatives.
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CSAM Studies
CSAM Studies, formerly known as MedSciNet Studies, is a robust and highly adaptable online platform that has demonstrated success in managing clinical studies and trials for two decades. This web-based environment for medical research provides an advanced suite of applications designed for the hosting, administration, and oversight of projects varying in scale and intricacy. The standard offering from CSAM MedSciNet includes all essential elements necessary to establish a fully operational study or clinical trial. Additionally, this benchmark solution is equipped with features that facilitate dynamic and interactive data entry forms, customizable workflow structures, and sophisticated capabilities for data validation, analysis, and exportation. By leveraging these tools, researchers can ensure a comprehensive and efficient approach to managing their clinical studies.
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