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Parkinson's Repository of Biosamples and Networked DatasetsPRoBaND(Tracking Parkinson's)Running title:Protein Protocol Version:1.5 Date:24/06/2016 REC Reference Number:11/AL/0163 Sponsors Protocol
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How to fill out parkinsons repository of biosamples

01
Visit the Parkinson's Repository of Biosamples website.
02
Click on the 'Register' button to create a new account or login if you already have an account.
03
Once logged in, click on the 'Submit Sample' option in the menu.
04
Fill out the required information for the sample, such as sample type, collection date, and donor information.
05
Attach any relevant files or documents related to the sample.
06
Review the information and make sure everything is correct.
07
Click on the 'Submit' button to complete the submission process.
08
You will receive a confirmation email once the sample submission is successful.

Who needs parkinsons repository of biosamples?

01
Researchers studying Parkinson's disease
02
Scientists looking for biomarkers or genetic information related to Parkinson's
03
Medical professionals and clinicians involved in Parkinson's research
04
Pharmaceutical companies developing new treatments for Parkinson's
05
Patients and patient advocacy groups interested in contributing to Parkinson's research

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The Parkinson's repository of biosamples is a collection of biological samples, such as blood, tissue, and other bodily fluids, used for research purposes to study Parkinson's disease and its progression.
Researchers and institutions involved in Parkinson's disease studies that collect and store biosamples are required to file the Parkinson's repository of biosamples.
To fill out the Parkinson's repository of biosamples, follow the guidelines provided by the overseeing authority, ensuring all required fields are completed accurately, including sample source, participant information, and intended research use.
The purpose of the Parkinson's repository of biosamples is to facilitate research on Parkinson's disease, aiding in the understanding of its causes, progression, and potential treatments by providing access to standardized biological samples.
Information that must be reported includes the type and quantity of biosamples collected, details of the participants (with necessary consent), storage conditions, and intended research applications.
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