Get the free Research Services Clinical Trial Routing Form - research utmb

This document serves as a routing form for clinical trials requiring UTMB approval, detailing sponsor information, principal investigator details, certifications, and approval signatures.

How to fill out research services clinical trial

How to fill out Research Services Clinical Trial Routing Form

1. Step 1: Obtain the Research Services Clinical Trial Routing Form from the appropriate departmental website or administrative office.
2. Step 2: Fill in the title of the clinical trial at the top of the form.
3. Step 3: Provide the names and contact information of the principal investigator and any co-investigators.
4. Step 4: Indicate the grant number or funding source associated with the clinical trial.
5. Step 5: Include details about the clinical trial design, objectives, and procedures, including eligibility criteria.
6. Step 6: Fill in information regarding the study population, including the estimated number of participants.
7. Step 7: Attach any relevant documents, such as the study protocol, informed consent forms, and funding application.
8. Step 8: Review the completed form for accuracy and completeness.
9. Step 9: Submit the form and attached documents to the Research Services office for review and approval.

Who needs Research Services Clinical Trial Routing Form?

1. Principal investigators planning to conduct clinical trials.
2. Co-investigators involved in the research process.
3. Research coordinators managing the logistics of the trial.
4. Administrative staff supporting the research process.

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For pdfFiller’s FAQs

What is Research Services Clinical Trial Routing Form?

The Research Services Clinical Trial Routing Form is a document used to facilitate the approval and routing of clinical trials within a research organization. It serves as a formal request to initiate the evaluation process for a proposed clinical study.

Who is required to file Research Services Clinical Trial Routing Form?

The form is typically required to be filed by researchers or principal investigators who are proposing a new clinical trial that needs institutional review and approval before initiation.

How to fill out Research Services Clinical Trial Routing Form?

To fill out the form, the researcher must provide details such as study title, objectives, study design, funding sources, participating sites, and any associated risks. They may also need to provide ethical approval details and signatures from necessary department heads.

What is the purpose of Research Services Clinical Trial Routing Form?

The purpose of the form is to ensure that clinical trials are properly reviewed, approved, and monitored in accordance with institutional policies and regulations, safeguarding participant welfare and ensuring compliance with legal and ethical standards.

What information must be reported on Research Services Clinical Trial Routing Form?

Information that must be reported includes study title, principal investigator information, a detailed description of the trial, objectives, methodologies, risk assessments, funding sources, and any other relevant documentation required by the institution.