## Where a successful trial launch begins its ascent

To optimize the study start-up process, automate it. Removing manual tracking streamlines the processes to eliminate aggravating bottlenecks and ensure quality from the start.

## Benefits

- Fully configurable to optimize processes
- Automates the study startup process
- Templates provide critical regulatory knowledge
- Enables the team to meet timelines by focusing on critical path items
- Increases end-to-end visibility of study lifecycle
- Enhances communication between teams (e.g., start-up, regulatory, and clinical)

## Features

- Investigator database with site creation and contact management
- Activity and document tracking in a managed, validated system including IP tracking
- Pre-defined country submission documents and expected approval timelines
- Built-in project management critical path with associated timelines
- Status sharing internally and to customers via direct access and/or APIs to local systems
- Manage Investigator DB at the institutional level– BENEFIT of this Ensures data quality and eliminates duplicate entries

[DOWNLOAD BROCHURE](/content/study-start-up-2/index.html)

## Configurable Applications

### Study Start-Up + CTMS

Eliminate communication gaps and missed triggers between startup and clinical groups. No more relying on email and spreadsheets for crucial site qualification visits and site initiation visits.

### Study Start-Up + RBQM

Launch your study with data quality and risk mitigation in mind. Quickly collaborate with your team and gain the visibility you need for effective startup and quality control.

### Study Start-Up + RBQM + CTMS

Take your clinical trial to the next level by adding RBQM. Now you can effectively manage your study data from the first site identification to the last patient visit.

[BOOK A DEMO](/content/book-a-demo/index.html)