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. How simple and user-friendly is it? Ask for a demo to find out! Clinvigilant💊, your one-stop 🌐solutions provider for ☁️clinical trials. Enquiries > bd (at) clinvigilant.com

Meet the leading-edge validation solution that automates, unifies, and accelerates your success. Res_Q helps IT and quality leaders eliminate validation debt, achieve peace of mind, and untangle valuable resources. Res_Q’s data-focused architecture and a wide array of industry-supported applications prevent you from falling deeper into validation debt with every new software release. The open API approach unlocks a bi-directional data flow that empowers system integrations, migration during onboarding, and more. Configurable workflows to both match your operational requirements and integrate industry best practices. All validation processes are controlled in a single system, serving all areas across the enterprise, including IT, manufacturing, lab systems, and more. Initiate workflows and assign workloads based on risk profile. Res_Q puts quality at the forefront without sacrificing speed.