Managing trials can be complicated. Throughout the research process, we automate outdated clinical trial management software to increase its accuracy, efficiency, and data collection capabilities.
We improve data security and transparency by incorporating blockchain into current clinical data systems, providing tamper-proof records and efficient data sharing among stakeholders.
Trial documentation needs to be well-organized. ProcesIQ automates eTMF processes, interfacing with document management systems to make storage, retrieval, and regulatory audits easier.
Drug safety monitoring is essential. We complement current pharmacovigilance systems with automation, accelerating detection of adverse drug reactions and enhancing patient safety.
Compliance with regulations is complicated. We automate compliance reports through integration with current regulatory ERPs to ensure smooth submissions and guideline compliance.
Regulatory actions can be slow and labor-intensive. ProcesIQ automates them by bridging AI-powered automation with existing pharma software, speeding up approvals, and lowering compliance risk.
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