OpenClinica Integrations

Enhance the efficiency of your clinical studies with Clinvigilant, your global provider of budget-friendly eClinical tools tailored for CROs, Pharma, Biotech, Nutraceuticals, and academic institutions throughout both clinical and post-marketing phases. Our clients consistently choose to partner with us due to our: ♦ Rapid EDC implementation (under 4 weeks). ♦ Cost-effective solutions. ♦ Integration capabilities with third-party and legacy systems. Our cloud-based platform, hosted on Microsoft Azure, adheres to HIPAA, ICH-GCP, GDPR, and 21 CFR part 11 regulations and has successfully undergone audits by the FDA, EMA, and MHRA. The Clinvigilant eClinical suite encompasses a variety of tools, including EDC, CTMS, eCRF, eTMF, eSource, IWRS, ePRO, eConsent, and eCOA. You can select the specific tools you require, and we will seamlessly integrate them into your existing software framework. Each interaction and data exchange generates detailed Audit Trails, ensuring real-time visibility of compliant data across all relevant roles. Our offerings are modular, highly customizable, and accessible via web, iPad, and mobile applications for both Android and iOS platforms. Additionally, we support the use of Patient's Own Devices (BYOD) and can interface with various devices and wearables for enhanced data collection. With Clinvigilant, you can count on a comprehensive solutions provider to streamline your clinical trial processes effectively and efficiently. Your success in clinical research begins here.

Uncover the groundbreaking validation solution aimed at automating, consolidating, and accelerating your accomplishments. Res_Q aids IT and quality leaders in removing validation debt, fostering peace of mind, and optimizing the use of valuable resources. Featuring a data-focused architecture and a broad spectrum of applications across various sectors, Res_Q helps you avoid accumulating validation debt with every new software update. Its open API framework allows for seamless bi-directional data exchange, improving system integrations and simplifying migration during the onboarding phase. Customized workflows are designed to meet your specific operational requirements while integrating industry best practices effortlessly. Each validation process is handled within a cohesive system that serves all facets of the organization, including IT, manufacturing, laboratory systems, and more. You can kickstart workflows and assign tasks according to the risk assessment, ensuring that quality remains paramount without sacrificing efficiency. By adopting Res_Q, organizations not only boost their operational productivity but also cultivate a mindset of ongoing improvement, leading to sustained success. This comprehensive approach ultimately positions businesses to respond swiftly to evolving industry demands while maintaining high-quality standards.