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NSW Health Pathology Victorian Clinical Genetics Services SA PathologyPARTICIPANT CONSENT INFORMATION SHEET AND CONSENT Forth Economic and Personal Impacts of Genomic Testing in Pregnancy Invitation You

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How to fill out clinical genomic testing consent

01

Read the consent form thoroughly to understand the information provided.

02

Ask any questions you may have about the testing or the consent form.

03

Sign and date the consent form to indicate your agreement to undergo the testing.

Who needs clinical genomic testing consent?

01

Individuals who are undergoing clinical genomic testing to determine genetic predispositions or mutations.

02

Researchers conducting genomics studies on human subjects.

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What is clinical genomic testing consent?

Clinical genomic testing consent is a document signed by a patient or their legal guardian, giving permission for genomic testing to be conducted.

Who is required to file clinical genomic testing consent?

Patients or their legal guardians are required to file clinical genomic testing consent.

How to fill out clinical genomic testing consent?

Clinical genomic testing consent can be filled out by providing personal information, signing the document, and acknowledging understanding of the testing process.

What is the purpose of clinical genomic testing consent?

The purpose of clinical genomic testing consent is to ensure that patients understand the risks and benefits of genomic testing and give informed consent for the procedure.

What information must be reported on clinical genomic testing consent?

Clinical genomic testing consent must include information about the purpose of the testing, potential risks and benefits, and privacy regulations.

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