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This document outlines a study aimed at developing a wearable device to monitor and prevent overuse injuries in youth athletes, particularly in baseball. The study will involve collecting motion-capture data from young pitchers to create algorithms for tracking and analyzing their throwing movements and related injury risks. It details study objectives, design, procedures, safety management, and data handling protocols.
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01
Obtain the throwing device trial form from the relevant authority or organization.
02
Gather all necessary personal information, including name, address, and contact details.
03
Fill in the details about the throwing device you are testing, including make, model, and specifications.
04
Provide any required medical documentation or proof of need for the throwing device.
05
Include information about any previous trials or therapy related to the throwing device.
06
Sign the form and date it.
07
Submit the completed form to the designated review board or committee.

Who needs throwing device trial?

01
Individuals with physical or mobility impairments who require assistance in throwing objects.
02
Therapists who need to evaluate the effectiveness of a specific throwing device for their clients.
03
Manufacturers seeking feedback on their products through user trials.
04
Research institutions conducting studies on adaptive technologies.
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A throwing device trial is a legal process used to evaluate the effectiveness and safety of throwing devices, often in the context of regulatory compliance or product liability.
Manufacturers or distributors of throwing devices are typically required to file a throwing device trial to demonstrate compliance with relevant safety and performance standards.
To fill out a throwing device trial, the applicant must provide detailed information about the device, including specifications, testing results, and any incident reports, along with relevant supporting documentation.
The purpose of a throwing device trial is to assess the device's safety, functionality, and compliance with regulatory standards, ensuring that it meets the required criteria for market launch or use.
The information reported must include device specifications, test results, compliance documents, incident history, and any modifications made to the device during testing.
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