RegDesk
RegDesk stands out as the leading RIMS platform enhanced by AI, tailored specifically for Medical Device, Pharmaceutical, and IVD companies.
• Our unique Regulatory Intelligence encompasses data from over 120 countries, all presented in a uniform format, and includes timely alerts regarding regulatory updates.
• With our AI-driven Application Builder, regulatory affairs teams can efficiently create and submit global applications in a fraction of the usual time.
• The Change Assessment feature enables RA teams to evaluate the implications of changes on current products and determine the necessary actions.
• Our Distributor Collaboration tool facilitates smooth workflows for communication and document sharing with external partners.
• The Standards Management function simplifies the process for RA teams to locate and oversee both international and country-specific standards.
• Additionally, our Tracking & Reporting capability empowers teams to monitor regulatory initiatives worldwide, receive notifications for renewals, and quickly compile reports on key performance indicators.
To learn more about our offerings, please explore our website.
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Incredable
Incredable serves as a comprehensive and customizable credentialing platform that connects healthcare facilities, providers, and administrators effectively. The solution simplifies the credentialing workflow by managing documents, tracking compliance, and verifying credentials seamlessly. By using Incredable, healthcare professionals can maintain their compliance and readiness consistently. Widely recognized in the healthcare sector, Incredable alleviates the strain of administrative tasks, boosts operational productivity, and promotes smooth collaboration among all parties involved, enabling healthcare teams to concentrate on providing exceptional patient care. Furthermore, this innovative solution adapts to various healthcare needs, making it an invaluable tool in today’s dynamic environment.
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dilisense
Meet your obligations related to AML, KYC, and CTF with the innovative solution offered by dilisense.
For compliance professionals, navigating the complex landscape of sanctions along with various regulations like AML, KYC, and CTF can be quite daunting. dilisense provides an efficient and reliable platform for sanctions screening and Politically Exposed Persons (PEP) checks, ensuring that your organization stays compliant while effectively managing potential risks.
Our extensive sanctions database includes listings from OFAC, EU, OFSI, UN, and more, aggregating over 80 distinct sanction lists. Moreover, our database for PEPs and criminal watchlists draws from a vast array of global, regional, and local sources.
With dilisense, you gain access not only via a REST API but also have the option to download the entire database directly to your systems, with regular updates occurring multiple times daily.
At an attractive starting price of just 0.01 EUR per screening, the financial impact of compliance and sanctions screening becomes minimal, allowing for more strategic allocation of resources.
To ensure you can start immediately, we also offer Batch Screenings directly from Excel files, eliminating the need for any integration or setup, thus allowing you to begin your compliance measures without delay. This ease of access empowers organizations to take proactive steps in managing their compliance responsibilities.
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Veeva Vault RIM
The Vault RIM Suite provides a robust platform for comprehensive management of regulatory information throughout its entire lifecycle. By consolidating global regulatory workflows within a cloud-based infrastructure, it significantly improves visibility, data integrity, and responsiveness for organizations in the life sciences sector. This centralization enables companies to quickly adjust to evolving regulations while enhancing efficiency during the submission process, from initial planning to final publication. Moreover, the platform fosters seamless collaboration among headquarters, affiliates, and partners, all integrated within a singular RIM system. It ensures that regulatory teams produce content that is trustworthy and maintains the highest standards of data quality. Veeva Vault Registrations manages product registration information globally, including registration status, variations, and interactions with health authorities, while its flexible data model is prepared to integrate IDMP data points and adapt to shifts in regulatory data standards. Additionally, Veeva Vault Submissions streamlines the submission planning process by automating numerous steps in the regulatory workflow, resulting in considerable time savings and enhanced outcomes. This comprehensive approach ultimately empowers companies to navigate the intricate landscape of regulatory compliance with increased ease and accuracy, reinforcing their capacity to succeed in a competitive environment. As regulatory landscapes continue to evolve, this platform positions organizations to stay ahead of the curve.
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