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Patient Informed Consent for Genetic Testing International Hereditary CancerEffective Date September 29, 2016IMPORTANT HEALTHCARE PROFESSIONALS: The U.S. Testing Laboratory will only accept ANONYMIZED
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01
Start by obtaining a testing laboratory's signed copy of this consent form.
02
Make sure the laboratory does not provide you with a copy of the form.
03
Fill out the form accurately and legibly.
04
Provide any necessary information as requested on the form.
05
Ensure that all sections of the form are completed properly.
06
Double-check your entries for any errors or missing information.
07
Sign and date the form at the designated spaces.
08
Return the completed and signed form to the appropriate recipient or entity.
09
Keep a copy of the completed form for your records, if necessary.
Who needs testinglaboratorybretainasignedcopyofthisconsentandnotprovideacopytoform?
01
The testing laboratory needs to retain a signed copy of this consent form and not provide a copy to the form.
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What is testinglaboratorybretainasignedcopyofthisconsentandnotprovideacopytoform?
Testing laboratory must retain a signed copy of this consent and not provide a copy to form.
Who is required to file testinglaboratorybretainasignedcopyofthisconsentandnotprovideacopytoform?
All testing laboratories are required to file a signed copy of this consent.
How to fill out testinglaboratorybretainasignedcopyofthisconsentandnotprovideacopytoform?
The testing laboratory should have the individual sign the consent form and retain the signed copy.
What is the purpose of testinglaboratorybretainasignedcopyofthisconsentandnotprovideacopytoform?
The purpose is to ensure that the individual has given consent for testing and the laboratory has documentation of this consent.
What information must be reported on testinglaboratorybretainasignedcopyofthisconsentandnotprovideacopytoform?
The signed consent form with the individual's information and signature.
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