OpenClinica Integrations

Streamline your clinical studies with Clinvigilant, your global cost-effective eClinical tools provider for CROs, Pharma, Biotech, Nutraceuticals and Academic organizations in clinical and post-marketing stages. Most of our clients choose and stay with us for thanks to our: ♦ Fast EDC set-up (less than 4 weeks). ♦ Cost-effectiveness. ♦ 3rd party integrations (including legacy systems). Our cloud-based suite (Microsoft Azure) is HIPAA, ICH-GCP, GDPR & 21 CFR part 11 compliant and we have been audited by the FDA, EMA and MHRA. The Clinvigilant eClinical suite includes: EDC, CTMS, eCRF, eTMF, eSource, IWRS, ePRO, eConsent and eCOA. Just pick the tools that you need and we will integrate them within your existing software ecosystem. Every interaction and data exchange creates Audit Trails, which provide compliant real-time data visibility across all relevant roles. Our products are modular, highly customizable, and available on the web, iPad, and Mobile App for both Android and iOS. We also support Patient's Own Device (BYOD) and interface with Devices and Wearables. Clinvigilant💊, your one-stop🌐solutions provider for clinical trials☁️ .

Discover the innovative validation solution designed to automate, unify, and expedite your achievements. Res_Q assists IT and quality leaders in eliminating validation debt, ensuring tranquility, and allocating valuable resources effectively. With its data-centric architecture and extensive range of applications supported by various industries, Res_Q prevents you from deepening your validation debt with each new software release. The open API framework facilitates a bi-directional data exchange, which enhances system integrations and streamlines migration during the onboarding process. Tailored workflows are available to align with your operational needs while incorporating industry best practices seamlessly. Every validation procedure is managed within a unified system that caters to all sectors of the organization, such as IT, manufacturing, lab systems, and beyond. You can initiate workflows and delegate tasks based on the risk profile, ensuring that quality remains a priority without compromising on speed. By leveraging Res_Q, organizations can enhance their operational efficiency and foster a culture of continuous improvement.

BioGRID serves as an advanced clinical data management platform and visual analytics solution aimed at simplifying the handling of clinical data while enhancing the decision-making process. By integrating cutting-edge AI technology with user-friendly visualizations, robust compliance features, and efficient workflows for clinical trials, it creates a cohesive environment. This tool consolidates a variety of clinical data sources, allowing for uninterrupted data ingestion, trend identification, forecasting, and predictive analytics that assist teams in recognizing patterns and potential risks, thus fostering proactive decision-making. Additionally, BioGRID offers thorough oversight of studies, providing comprehensive views of both progress and outcomes, along with automated patient tracking systems and resources for effective medical and statistical evaluations. It also incorporates proactive data surveillance and risk-based quality management capabilities, which help maintain data integrity and compliance with industry regulations, including the monitoring of key risk indicators, identifying possible discrepancies, and maintaining audit trails. Ultimately, BioGRID empowers clinical teams to navigate complex data landscapes with confidence and precision.