Create your Trial Related Form from scratch

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Here's how it works

01. Start with a blank Trial Related Form
Open the blank document in the editor, set the document view, and add extra pages if applicable.
02. Add and configure fillable fields
Use the top toolbar to insert fields like text and signature boxes, radio buttons, checkboxes, and more. Assign users to fields.
03. Distribute your form
Share your Trial Related Form in seconds via email or a link. You can also download it, export it, or print it out.

A simple tutorial on how to set up a polished Trial Related Form

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Step 1: Log in to DocHub to begin creating your Trial Related Form.

First, log in to your DocHub account. If you don't have one, you can easily register for free.

Step 2: Navigate to the dashboard.

Once you’re in, go to your dashboard. This is your primary hub for all document-focused tasks.

Step 3: Initiate new document creation.

In your dashboard, choose New Document in the upper left corner. Hit Create Blank Document to craft the Trial Related Form from scratch.

Step 4: Add template fillable areas.

Add numerous fields like text boxes, images, signature fields, and other elements to your template and assign these fields to intended users as necessary.

Step 5: Personalize your document.

Customize your document by adding guidelines or any other required details using the text feature.

Step 6: Double-check and tweak the document.

Carefully check your created Trial Related Form for any inaccuracies or essential adjustments. Utilize DocHub's editing features to fine-tune your document.

Step 7: Send out or download the document.

After finalizing, save your work. You may opt to retain it within DocHub, export it to various storage services, or send it via a link or email.

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We have answers to the most popular questions from our customers. If you can't find an answer to your question, please contact us.
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Though FDA Form 3674 has been required for nearly all data submitted to the FDA since December 2007, it is not nearly as well recognized. The form is a notification of compliance signifying that the trials have been correctly registered and documented on clinicaltrials.gov (CT. Sure, You Know All About FDA Form 1572 - But What About Form 3674? The Bracken Group blog sure-you-kn The Bracken Group blog sure-you-kn
The investigators signature on the form confirms his or her qualification and commitment to conduct the clinical investigation ing to the FDA regulations.
In general, if an individual is directly involved in the performance of procedures required by the protocol, and the collection of data, that person should be listed on the Form FDA 1572.
In January 2021, following discussions with EORTC, NCI have launched a new International Investigator Statement (IIS) in the Registration and Credential Repository (RCR) for European countries. This statement replaces the Form FDA 1572 for participation in US NCTN and NCORP trials that are not under IND.
Therefore, the correct answer to the students question is B. Addition of a new investigator, since the FDA Form 1572 must be filed to include information on any new personnel joining the research team.
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Related Q&A to Trial Related Form

How to Design a Clinical Trial: 5 Steps Make it simple. Patient and associated professionals recruitment is a key determinant of success. Plan the 4 phases with the goal of your clinical trial in mind. Develop an adequate budget and resources plan. Try to poke holes on your design and protocols. How to Design a Clinical Trial: 5 Steps - Kolabtree Kolabtree blog how-to-design-a-clin Kolabtree blog how-to-design-a-clin
A form that must be filed by an investigator running a clinical trial to study a new drug or agent. The investigator agrees to follow the U.S. Food and Drug Administration (FDA) Code of Federal Regulations for the clinical trial. Form FDA 1572-Statement of Investigator - National Cancer Institute National Cancer Institute dictionaries cancer-terms def National Cancer Institute dictionaries cancer-terms def
Complete form 3454 if none of the investigators have any FDA required disclosures. Complete form 3455 if any clinical investigator has a financial disclosure that is docHub. Sponsor Instructions for Completion of Financial Interests for VCU/VCUHS vcu.edu instructionsCOImanagement vcu.edu instructionsCOImanagement

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