MAISi

The core functionality of MAISi, designed to manage all aspects of clinical trials at investigator sites. This provides a centralized platform for trial management.

Stores information about studies and the business units that run them. This centralizes data for better organization and decision-making.

Guides users through processes like study start-up, ensuring compliance and consistency. This automates and streamlines key processes.

Helps track the feasibility of potential studies. This assists in the early planning stages of a trial.

Manages the ethics approval process. This simplifies compliance with regulatory requirements.

Simplifies the recording of patient visits and associated assessments. This streamlines data collection and management.

Lists procedures with associated costs and third-party providers. This facilitates budget creation and financial tracking.

Creates budgets based on the cost of investigative procedures and visit templates. This helps in financial planning.

Allows users to monitor and correct invoices from third-party providers. This ensures accurate financial records.

Tracks ongoing costs and income for a study. This provides real-time financial insights.

Compares costs and income at the patient visit level. This allows for detailed financial analysis.

Supports the generation of three types of invoices. This simplifies billing processes.

Manages patient reimbursements. This ensures timely and accurate payments.

Provides checklists for patient visits. This helps ensure all necessary steps are taken.

Generates letters to patients and their GPs. This improves communication and patient care.

Allows for customization of the document storage and retrieval system. This provides flexibility for different site needs.

Supports ad-hoc reporting through searchable fields. This enables users to generate custom reports as needed.

Allows data to be exported to spreadsheets. This facilitates further analysis and reporting.