Looking for alternatives or competitors to EXTEDOPulse? Other important factors to consider when researching alternatives to EXTEDOPulse include reliability and ease of use. The best overall EXTEDOPulse alternative is MasterControl Quality Management System. Other similar apps like EXTEDOPulse are Clinical Research Suite, Kivo, Rimsys, and Veeva Vault RIM. EXTEDOPulse alternatives can be found in Regulatory Information Management (RIM) Systems but may also be in Quality Management Systems (QMS) or Clinical Trial Management Systems.
MasterControl Inc. produces QMS software solutions which enable regulated companies to get their products to market faster, while reducing overall costs and increasing internal efficiency. MasterControl securely manages a company's critical information throughout the entire product lifecycle.
Research Manager supports researchers and organisations in preparing, executing and administering (clinical) research data. Our expertise is the collection, validation and enrichment of data. With Research Manager, we offer a research platform that allows researchers to have all functionalities and information in one place and to share it with each other. The platform facilitates researchers who want to be prepared for a future where the patient, access to data, and sharing data are key.
Kivo makes simple and affordable document management systems including RIM, eTMF, and QMS. A single license grants access to all our solutions, so you can supercharge cross-functional collaboration without breaking the bank. Fully validated, Part 11 and SOC 2 compliant, Kivo is designed forGxP.
The Vault RIM Suite provides fully integrated regulatory information management (RIM) capabilities on a single cloud-based platform including submission document management, product registration management, health authority correspondence and commitments, submission archiving, and comes with fully integrated IDMP capabilities.
RegDesk is the next generation RIMS software with AI technology built exclusively for medical device and diagnostic companies. It is a one stop solution for regulatory teams.
IQVIA RIM Smart is a comprehensive Regulatory Information Management (RIM solution designed to streamline and enhance regulatory processes for life sciences organizations. It offers a unified platform that integrates various regulatory functions, enabling efficient management of product registrations, submissions, and compliance activities. Key Features and Functionality: - Centralized Regulatory Data Management: Provides a single source of truth for all regulatory information, ensuring data consistency and accuracy across the organization. - Submission Planning and Tracking: Facilitates the planning, preparation, and tracking of regulatory submissions, improving efficiency and reducing time to market. - Compliance Monitoring: Automates compliance checks and monitors regulatory requirements to ensure adherence to global standards. - Workflow Automation: Streamlines regulatory workflows through automation, reducing manual efforts and minimizing errors. - Reporting and Analytics: Offers robust reporting tools and analytics to provide insights into regulatory activities and support informed decision-making. Primary Value and User Benefits: IQVIA RIM Smart addresses the complexities of regulatory management by providing a centralized and automated solution that enhances efficiency, ensures compliance, and accelerates time to market for life sciences products. By integrating various regulatory functions into a single platform, it reduces manual efforts, minimizes errors, and provides real-time visibility into regulatory activities, enabling organizations to make informed decisions and maintain a competitive edge in the industry.
FDA Tracker by Leucine is an AI-powered platform that helps pharmaceutical and life sciences companies stay ahead of regulatory risks. With real-time insights into FDA inspection trends, 483 observations, and warning letters, FDA Tracker empowers teams to benchmark performance, uncover hidden risks, and proactively close compliance gaps—before the regulator comes knocking. Key Features Real-Time Inspection Data: Access the latest FDA inspections, 483s, and warning letters across facilities and regions. Company & Site-Level Insights: Drill down into specific companies or sites to benchmark against industry peers. AI-Powered Risk Signals: Spot emerging compliance risks and common failure patterns using smart analytics. Search & Filter with Precision: Find exactly what you need—by product type, region, observation code, and more. Compliance Heatmaps & Dashboards: Visualize performance trends and identify red flags in seconds. Exportable Reports: Create shareable reports for internal audits, board reviews, or inspection readiness plans. Business Impact Proactively Close Compliance Gaps with early visibility into regulatory trends Benchmark Performance against industry peers and FDA expectations Enhance Audit Readiness by focusing on real-world inspection patterns Drive Smarter Quality Decisions with data-backed risk intelligence
RIMS (Regulatory Information Management System) allows companies to team up, preserve application information data from various locations and enhance the processes of preparing a submission, as well as simplify the publishing and tracking of all regulatory activities that support a product’s complete life cycle.
Validfor is a digital validation lifecycle management platform that modernizes how regulated organizations manage their computerized system validations. Designed for the life sciences, pharmaceutical, and medical device industries, Validfor centralizes all validation activities in one secure and compliant environment. By replacing traditional manual validation with a digital, data-driven approach, Validfor enables teams to plan, execute, and track validation processes with real-time visibility and accuracy. The platform includes built-in templates, electronic approvals, and full traceability to ensure regulatory compliance and consistent documentation quality. Whether you’re managing a single system or an enterprise-wide validation program, Validfor helps your organization stay audit-ready, improve collaboration, and maintain complete data integrity while saving time and reducing compliance risk.