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FORUM FOR ETHICAL REVIEW COMMITTEES IN ASIA AND THE WESTERN PACIFIC WHO TDR Clinical Coordination and Training Center (CCC), 1st Floor, Academic Affairs Building (Executive Office of University),

How to fill out sidcer form

How to fill out SIDCER:

1. Begin by gathering all the required information and documents needed to fill out the SIDCER form. This may include personal information, contact details, research objectives, study design, and ethical considerations.
2. Carefully read through the instructions provided with the SIDCER form. Familiarize yourself with the sections and fields that need to be completed.
3. Start by filling out the basic information section of the SIDCER form. This typically includes details like the title of the study, the name of the principal investigator, and the institutional affiliations.
4. Proceed to fill out the sections related to the research objectives and study design. Clearly state the purpose of the research, the hypothesis (if applicable), and the methods that will be used to collect and analyze the data.
5. Ensure that you provide sufficient information regarding the participant selection process and criteria in the appropriate section. This includes details on the inclusion and exclusion criteria, recruitment strategies, and the total number of participants planned for the study.
6. Next, carefully consider the ethical considerations section. Detail how the study will ensure the safety, privacy, and well-being of the participants. Provide information on how informed consent will be obtained and if any vulnerable populations are involved.
7. Review the completed SIDCER form for any errors or missing information. Double-check that all the sections and fields have been appropriately filled out according to the provided instructions.
8. After reviewing and correcting any mistakes, sign and date the Sidcer form as required. Make sure that all relevant stakeholders and partners have also signed the necessary sections.

Who needs SIDCER:

1. Researchers conducting human subjects research projects that involve international collaborations may need SIDCER. It provides a standardized ethical review process and guidelines to ensure the protection of human participants involved in the study.
2. Institutions or ethics committees responsible for overseeing research involving human subjects can benefit from SIDCER. It helps them establish a systematic approach to reviewing and approving research protocols, promoting ethical practices.
3. Funding agencies or organizations providing grants for research studies may require researchers to go through the SIDCER ethical review process. It ensures that the research project adheres to international ethical standards and guidelines.

In summary, filling out the SIDCER form involves gathering the necessary information, following the provided instructions, and paying attention to details in each section. Researchers, institutions, and funding agencies may all have a need for SIDCER in order to ensure ethical practices in human subjects research.

For pdfFiller’s FAQs

What is sidcer?

SIDCER stands for Structured Data Capture for Electronic Health Records.

Who is required to file sidcer?

Healthcare providers and facilities that use electronic health records are required to file SIDCER.

How to fill out sidcer?

SIDCER is filled out electronically using specific software that can capture structured data from electronic health records.

What is the purpose of sidcer?

The purpose of SIDCER is to standardize the capture of electronic health record data for research and analysis purposes.

What information must be reported on sidcer?

Information such as patient demographics, medical history, treatments, and outcomes must be reported on SIDCER.

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