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optivalue.aiStop letting RFPs, audits, and compliance questionnaires become a costly administrative burden that ties up your best experts. Optivalue.ai is designed to turn this process from a chore into a competitive advantage. Our intelligent platform automates information discovery and response drafting, slashing response times by up to 90%. This frees your most qualified team members to focus on the high-impact personalization that wins bids and ensures compliance. Optivalue.ai acts as an expert librarian for your entire knowledge base. It securely connects to your systems, reading and understanding every document to know precisely where the best information is. Submit any questionnaire and receive a complete, source-verified draft in minutes. But we go beyond simple automation to deliver proven answers. For perfect traceability and absolute confidence, every statement is backed by a precise citation—source document, page, and date. You don’t just answer correctly; you prove it. Furthermore, Optivalue.ai is your engine for organizational progress. It performs a proactive gap analysis—a true "pre-flight check" on your documentation—to identify weaknesses and inconsistencies before your clients or auditors do. The platform provides actionable recommendations that continuously build your team's expertise. By following these suggestions to update your internal documents, you drive lasting, measurable progress across your entire organization. Manage your data with total peace of mind. Optivalue.ai is built with enterprise-grade security, fully compliant with strict standards like GDPR, HIPAA, ISO, and FedRAMP. To simplify your decision and make your costs predictable, we’ve included a key advantage in all our plans: unlimited users and projects. Scale your operations without worrying about complex tiers or surprise fees. Start your 14-day free trial today. No credit card required. No commitment.
What is Evidex?
Efficiently monitoring a variety of data sources, in conjunction with a GVP IX compliant signal management system, can significantly enhance the way safety data is processed. The Evidex platform provides a comprehensive, ready-to-use solution that adheres to GVP-IX standards, allowing for smoother operations without the need to navigate through multiple services. By updating your management workflows, you can create processes that are both efficient and resistant to audits. This level of automation aids in fulfilling regulatory requirements while simultaneously increasing the overall benefits for your organization. Through the use of automated signal detection, safety signals can be recognized from key resources, such as ICSR databases and the FDA's Adverse Event Reporting System (FAERS), alongside VigiBase and clinical trial information. Additionally, you can enhance your data landscape by adding other sources like claims, electronic health records (EHR), and various forms of unstructured data. By combining these different data sources, you can enhance signaling algorithms, streamline validation processes, and respond more swiftly to urgent drug safety issues. Furthermore, this innovative approach redefines how organizations handle and utilize safety data, ultimately leading to improved results and a more proactive stance on drug safety management.
What is Dialog?
Dialog presents a thorough and adaptable solution for monitoring pharmacovigilance literature, aimed at improving the operational effectiveness of drug safety reporting organizations by automating and streamlining the literature triage process. It offers access to a vast array of over 140 esteemed scientific and medical literature databases, such as MEDLINE, Embase, and Biosis, which helps standardize content from diverse sources, thus ensuring a uniform approach to precision searching, deduplication, and structured XML output. The DialogML engine harnesses cutting-edge artificial intelligence to rank search results according to their relevance to patient safety, discern essential safety concepts, and categorize references related to Individual Case Safety Reporting (ICSRs), aggregated reports like PBRER, PSUR, and DSUR, as well as safety signals, allowing reviewers to quickly identify high-priority articles. Additionally, the Dialog Alerts Manager streamlines the alert creation and management process through features such as bulk editing capabilities, thorough audit trails for modifications in search strategies, customizable scheduling, and meticulous tracking of delivery histories. This cohesive system not only dramatically minimizes the time and effort needed for efficient literature monitoring but also empowers organizations to direct their attention toward more pressing drug safety concerns and enhance their overall reporting accuracy. Ultimately, this leads to improved patient safety outcomes and more effective regulatory compliance.
Integrations Supported
Amazon EC2
Amazon RDS
Amazon Web Services (AWS)
PostgreSQL
XML
Integrations Supported
Amazon EC2
Amazon RDS
Amazon Web Services (AWS)
PostgreSQL
XML
API Availability
Has API
API Availability
Has API
Pricing Information
Pricing not provided.
Free Trial Offered?
Free Version
Pricing Information
Pricing not provided.
Free Trial Offered?
Free Version
Supported Platforms
SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux
Supported Platforms
SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux
Customer Service / Support
Standard Support
24 Hour Support
Web-Based Support
Customer Service / Support
Standard Support
24 Hour Support
Web-Based Support
Training Options
Documentation Hub
Webinars
Online Training
On-Site Training
Training Options
Documentation Hub
Webinars
Online Training
On-Site Training
Company Facts
Organization Name
Advera Health Analytics
Date Founded
2010
Company Location
United States
Company Website
www.adverahealth.com
Company Facts
Organization Name
Clarivate
Company Location
United Kingdom
Company Website
clarivate.com/life-sciences-healthcare/research-development/pharmacovigilance-drug-safety/dialog/