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RegDeskRegDesk 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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YurbiIf you're in search of reporting software, look no further than Yurbi. This platform enables the transformation of your data into real-time dashboards and reports tailored for business users. With robust security measures in place, Yurbi ensures that your data remains protected at all times. Instead of a sales pitch, you'll engage with a technical expert who can provide insights and guidance. To explore whether Yurbi suits your needs, simply fill out the form below to arrange a demo or meeting. Yurbi stands out as a reporting solution that features clear pricing and a flat-rate model. Users benefit from live access to data dashboards and reports, requiring minimal technical support. Your data's security is prioritized along with various enterprise-level features to safeguard it. Additionally, this self-hosted reporting software offers a cost-effective alternative to similar products in the market. Competing with platforms like Tableau, Sisense, Board, and Phocas, Yurbi is an excellent choice among top database reporting tools for businesses seeking efficiency and reliability. With Yurbi, you can harness the power of your data without breaking the bank.
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Doc SheetsIntroducing Doc Sheets: Effortlessly Enhance Your Enterprise Lifecycle and Requirements Management Doc Sheets is an innovative and user-friendly software solution designed to streamline the complexities of enterprise lifecycle and requirements management. Its intuitive design, versatile features, and budget-friendly pricing allow organizations of all sizes to efficiently handle documentation and requirements throughout the entire product development process. Key Features: User-Friendly Interface: Designed for easy navigation, enabling both technical and non-technical users to minimize their learning curve. Requirements Tracking: Effectively capture, document, and prioritize requirements while ensuring traceability. Project Management: Efficiently plan and monitor tasks, milestones, and deliverables. Test Case Management: Create, categorize, and track test cases to guarantee comprehensive testing coverage. Lifecycle Management: Oversee the full development cycle from the initial planning phase all the way to product release. Customizable for Multiple Industries: Adapt the software to meet the specific needs of software development, embedded systems, medical devices, and beyond. Collaboration and Version Control: Facilitate real-time teamwork and maintain version control for better project outcomes. Cost-Effective Pricing: Offering budget-friendly options for organizations of any scale. Experience the benefits of Doc Sheets today and transform your management processes for the better!
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What is Oracle Argus?
Argus emerges as the leading and trustworthy solution for the effective management, analysis, and reporting of adverse event cases associated with both premarket and post-market pharmaceuticals, biologics, vaccines, devices, and combination products. By bolstering your case management functions, it incorporates advanced features such as integrated automation, streamlined workflows, and touchless processing options tailored to meet your specific requirements. This well-established solution guarantees adherence to global regulations and standards governing drugs, vaccines, and devices, including E2B(R3), E2B(R2), eVAERS, eMDR, MIR, and IDMP, making it a reliable choice for organizations across the globe. Users of Argus Advanced Cloud benefit from Oracle Analytics, an AI-powered tool designed to unveil critical insights and facilitate prompt, informed decision-making. As teams responsible for medicinal product safety confront the difficulties of rising caseloads, varied signal detection data sources, and shifting regulations, they are often constrained by limited budgets and resources, highlighting the necessity for efficient solutions like Argus. Furthermore, this platform not only supports organizations in upholding safety and compliance in a multifaceted environment but also enhances their operational efficiency for ongoing success. In conclusion, Argus is indispensable for organizations striving to navigate the complexities of product safety while maximizing their resource utilization.
What is Clienvo eTMF?
Clinevo's electronic Trial Master File (eTMF) provides a streamlined digital platform for the organization and archiving of documents, images, and various digital assets pertinent to clinical trials. This eTMF is designed with an integrated DIA reference model and adheres to regulatory requirements. In addition to this, Clinevo features the MICC Intake, a web-based tool tailored for Medical Information Call Centers (MICC) and Pharmacovigilance (PV) experts, enabling them to efficiently log, track, and manage Product Quality Complaints (PQCs), Medical Inquiries (MIs), and Adverse Events (AEs). Moreover, Clinevo Safety acts as a robust cloud-based system that simplifies the Pharmacovigilance process while ensuring compliance with regulations, covering PV Intake, Case Processing, Regulatory Submissions/AS2 Gateway, Analytics, and Safety Signals all within one unified platform. Additionally, the Clinevo Website Intake tool can be easily integrated with Sponsor or CRO websites, providing an intuitive web interface for consumers and reporters to access and submit reports effortlessly. This comprehensive range of tools not only streamlines clinical trial management but also significantly enhances safety reporting efficiency and effectiveness. Ultimately, Clinevo's innovative solutions are designed to meet the evolving needs of the clinical research landscape.
Integrations Supported
AccelSafety
Compier Literature Screening
Oracle Analytics Cloud
Integrations Supported
AccelSafety
Compier Literature Screening
Oracle Analytics Cloud
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
Oracle
Date Founded
1977
Company Location
United States
Company Website
www.oracle.com/life-sciences/safety-solutions/argus-safety-case-management/
Company Facts
Organization Name
Clinevo
Company Location
United States
Company Website
www.clinevotech.com
Categories and Features
Categories and Features
Clinical Trial Management
21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning