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What is inoPLAN?

Addressing any inconsistencies in the schedule promptly is even more vital than the initial planning phase itself. The inoPLAN APS (Advanced Planning and Scheduling) system utilizes advanced algorithms to automatically create an optimized production timetable. Unlike conventional MRP and MRP II systems, inoPLAN accommodates a limited capacity for scheduling resources. The plan is continuously updated and refined with each change that occurs, ensuring it remains relevant. Scheduling is carried out seamlessly based on available resources, removing the necessity for manual task allocation. The SaaS model not only provides immediate benefits but also offers long-term investment returns. With an intuitive tool, you can effortlessly select or design a plan for your new project, enabling you to swiftly assess various scenarios and their impact on other scheduled or ongoing endeavors. The system guarantees that the project and all related tasks are scheduled automatically. In the event of any task delays affecting the project timeline, you will receive timely notifications, keeping you well-informed. This proactive strategy significantly boosts overall project management effectiveness while reducing potential disruptions, allowing for smoother operation and better resource utilization.

What is eDeviation?

eDeviation offers a thorough suite of tools designed for the evaluation and management of Protocol Deviations, simplifying the journey from software development and validation to the collection of essential documentation and the exportation of data for the Trial Master File (TMF). This innovation significantly reduces the workload on clinical teams who may encounter risks associated with poorly evaluated or neglected protocol deviations, regardless of their frequency. As part of Ethical's eClinical Software Platforms, eDeviation® improves the precision and productivity of clinical trial oversight. The software can be customized to fit the unique needs of your research team, whether assessments are made by an independent committee or internally. Its built-in forms, workflows, and export capabilities guarantee compliance with GxP standards while promoting effective study management. Moreover, the platform supports real-time online collaboration among study teams, investigators’ sites, and committee members, which accelerates decision-making and ensures that protocol deviation assessments are addressed promptly. This collaborative environment not only streamlines processes but also fosters a culture of transparency and accountability in clinical trials. Ultimately, eDeviation® plays a crucial role in enhancing the integrity and efficiency of clinical research processes, leading to improved research outcomes.

Media

Media

Integrations Supported

Additional information not provided

Integrations Supported

Additional information not provided

API Availability

API Availability

Pricing Information

Pricing not provided
Free Trial Offered?

Pricing Information

Pricing not provided

Supported Platforms

SaaS

Supported Platforms

SaaS

Customer Service / Support

Standard Support
Web-Based Support

Customer Service / Support

Not specified

Training Options

On-Site Training

Training Options

Not specified

Company Facts

Organization Name

inoDIGIT

Company Location

Portugal

Company Website

www.inodigit.com/inoplan.html

Company Facts

Organization Name

eDeviation

Company Website

www.protocoldeviation.com/eDeviation-software

Categories and Features

Production Scheduling

Not specified

Categories and Features

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