Piedmont Healthcare Office of Research Services
This file contains essential information and guidelines from the Piedmont Healthcare Office of Research Services, including details on the Institutional Review Board and compliance requirements. It serves as a resource for researchers and participants involved in clinical studies. Users can find contact information, meeting schedules, and submission instructions.
Edit, Download, and Sign the Piedmont Healthcare Office of Research Services
Form
eSign
Add Annotation
Share Form
How do I fill this out?
To fill out this form, begin by gathering all necessary research documentation and information. Ensure you have the correct approvals from relevant departments. Finally, complete the submission form accurately and submit it according to the provided guidelines.
How to fill out the Piedmont Healthcare Office of Research Services?
1
Gather all necessary documents related to your research proposal.
2
Obtain required approvals from relevant Piedmont departments.
3
Accurately fill out the submission form with all required information.
4
Submit the filled form to the designated IRB inbox.
5
Confirm receipt of your submission and adhere to follow-up procedures.
Who needs the Piedmont Healthcare Office of Research Services?
1
Researchers conducting human subjects research.
2
Clinical trial sponsors requiring IRB compliance.
3
Students undertaking research projects.
4
Healthcare professionals involved in clinical studies.
5
Institutional officials overseeing research activities.
How PrintFriendly Works
At PrintFriendly.com, you can edit, sign, share, and download the Piedmont Healthcare Office of Research Services along with hundreds of thousands of other documents. Our platform helps you seamlessly edit PDFs and other documents online. You can edit our large library of pre-existing files and upload your own documents. Managing PDFs has never been easier.
Edit your Piedmont Healthcare Office of Research Services online.
You can edit this PDF on PrintFriendly by accessing the document within our PDF editor. Utilize various editing tools to make necessary changes directly to the content. Save your alterations to create a personalized copy of the document.
Add your legally-binding signature.
Signing the PDF on PrintFriendly is a streamlined process. Access the signature feature within the PDF editor to add your signature electronically. Once signed, save the document for your records or share it as needed.
Share your form instantly.
Sharing your PDF on PrintFriendly is easy and efficient. After editing or signing, use the sharing options to distribute the document to colleagues or stakeholders. You can share via email or other platforms directly from our service.
How do I edit the Piedmont Healthcare Office of Research Services online?
You can edit this PDF on PrintFriendly by accessing the document within our PDF editor. Utilize various editing tools to make necessary changes directly to the content. Save your alterations to create a personalized copy of the document.
1
Open the PDF in PrintFriendly's editor.
2
Utilize tools to modify text or images as needed.
3
Review the changes you’ve made for accuracy.
4
Click 'Save' to create your updated version.
5
Download or share the edited PDF directly from the platform.
What are the instructions for submitting this form?
To submit this form, please ensure that you have fully completed all required fields. Email your submission to the designated IRB inbox at irb@piedmont.org, or submit via the online portal available on our website. For physical submissions, mail to the Piedmont Research Office at 1968 Peachtree Road, NW, Suite 3025, Atlanta, GA 30309.
What are the important dates for this form in 2024 and 2025?
Important submission dates are set at least three weeks prior to each monthly IRB meeting. Adjustments may apply around holiday periods, so always check the current year calendar for the precise timeline. Ensure to submit proposals in line with these key dates to meet institutional requirements.
What is the purpose of this form?
The purpose of this form is to outline the procedural requirements and guidelines for researchers conducting studies involving human subjects at Piedmont Healthcare. It ensures ethical review by the Institutional Review Board (IRB) to protect the rights and welfare of participants. Compliance with these guidelines not only facilitates research advancement but also adheres to federal regulations governing human subjects research.
Tell me about this form and its components and fields line-by-line.
- 1. Research Proposal: Details of the research study, including objectives and methodology.
- 2. Informed Consent Forms: Documents that disclose information to participants about the research.
- 3. IRB Membership Roster: List of IRB members with their qualifications.
- 4. Budget Justification: Justification for funding and resource allocation within the study.
- 5. Protocol: The detailed plan of the research design, methodology, and analysis.
What happens if I fail to submit this form?
Failure to submit this form may result in delays in the research approval process. As a result, your research timeline could be adversely affected, and you may miss critical deadlines.
- Funding Delays: Research funding may be jeopardized due to incomplete submissions.
- Regulatory Compliance: Non-compliance may lead to regulatory scrutiny.
- Participant Recruitment Issues: Delays in approval can hinder timely participant recruitment.
How do I know when to use this form?
- 1. For Clinical Trials: Use this form to seek IRB approval for clinical studies involving participants.
- 2. For Student Research Projects: Students must submit their research proposals via this form for review.
- 3. For Industry-Sponsored Studies: Industry partnerships require the use of this form to initiate the IRB process.
Frequently Asked Question
What is the purpose of this PDF?
This PDF provides guidelines for researchers on how to submit proposals to the Piedmont Healthcare IRB.
How can I edit the PDF?
Use the PrintFriendly editor to access various editing functions to modify your document.
Can I share the PDF after editing?
Yes, PrintFriendly allows you to share edited PDFs via email or other platforms directly.
What is the process for submitting this form?
Follow the guidelines provided within the document to ensure your submission is properly formatted.
Who needs this form?
Researchers, sponsors, and students involved in human subjects research require this form for submission.
How do I know if my submission was received?
Confirm receipt by following up with the designated IRB contact after submission.
What happens if I don't submit the form on time?
Late submissions may delay the review process and affect research timelines.
Are there fees associated with the IRB review?
Yes, there are fees for review services which are not contingent upon approval.
Can I access past submissions?
Refer to your institutional guidelines on record retention for past submission access.
How often is this document updated?
Updates are made regularly to reflect changes in policies and procedures.
Related Documents - Piedmont ORS Guidelines
Piedmont Healthcare Patient Registration File
This file contains essential patient registration forms and questionnaires for Piedmont Healthcare. It includes vital patient information, insurance details, and financial agreements. Utilize this file to streamline patient registration processes and ensure accurate information collection.
Management of Research Study Protocol Submission
This file provides detailed Standard Operating Procedures for the submission of research study protocols and related documents. It outlines the responsibilities of the Institutional Ethics Committee (IHEC) and the process for managing submissions. Ideal for researchers and administrative staff involved in research documentation.
Dominican University Research Participant Consent Form
This document provides essential consent forms for research participation at Dominican University of California. It outlines the rights and responsibilities of research participants. Included are guidelines for various research scenarios, ensuring ethical standards are met.
Summer Research Fellowship Program Proposal Form
This file contains the administrative form for the Summer Research Fellowship Program. It is designed for principal investigators and departments to propose summer research projects. The form includes sections for project details, compliance regulations, and evaluations.
HIPAA Authorization for Research in the USA
This file provides guidance on HIPAA Authorization for research purposes. It outlines the essential elements required for authorization and how to properly use patient health information. Intended for researchers and healthcare providers, this document ensures compliance with privacy laws.
IRB Application for Greater Than Minimal Risk Research
The IRB Application form is essential for research projects involving greater than minimal risk. This document guides investigators through compliance with research protocols. It includes vital information about the project, investigators, and required approvals.
Piedmont Technical College Plus One Application Form
This file contains the application form for the Plus ONE program at Piedmont Technical College. It provides essential information and requirements for students pursuing a degree in teacher education. Make sure to follow the instructions carefully for a successful application.
Human Subjects Consent Form Sample for Research
This file contains a sample Human Subjects Consent Form used for research studies. It outlines key information necessary for potential participants. Understanding this form is essential for ethical participation in research.
Research Statement Template for Academic Applications
A comprehensive guide on how to craft a research statement for academic faculty positions, detailing structure, content, and tips for merging research with teaching statements.
Express Interest in Higher Degree Research at JCU
This form enables prospective candidates to express their interest in applying for a higher degree by research at James Cook University. It is designed for those without a primary advisor and seeks to gather essential information for consideration. Completing this form does not guarantee acceptance, but initiates the inquiry process.
