From d6cf00e7fe913c26b48463a7373a4a02d828b1b7 Mon Sep 17 00:00:00 2001
From: Malte Lenger <malte.lenger@uni-bielefeld.de>
Date: Thu, 21 Nov 2024 18:03:34 +0100
Subject: [PATCH] safety seite anpassung text patient consent und cell culture
guide
---
src/contents/safety.tsx | 10 +++++-----
1 file changed, 5 insertions(+), 5 deletions(-)
diff --git a/src/contents/safety.tsx b/src/contents/safety.tsx
index e76e33b7..6ba698e3 100644
--- a/src/contents/safety.tsx
+++ b/src/contents/safety.tsx
@@ -217,14 +217,14 @@ export const Safety: React.FC = () =>{
</div>
</Subesction>
<Subesction title="Consent and Guidelines" id="Bioethics3">
+ <p></p>
+ <p>When working with primary cultures, it is extremely important to consider the bioethical aspects of the project. To address this, we sat down with the Ethics Officer at Bielefeld University, Dr. Berens, and discussed the matter with her. From this exchange, we gained the following insights.
+ On the one hand, having a patient consent form is crucial, as it provides the donors of the primary cells with a sense of security, but more importantly, it gives them detailed and precise information about what will be done with the data, whether it be regular patient data or biomaterials. Additionally, it became clear that it is significantly easier for us to establish guidelines to follow. We decided to integrate this approach into our project.
+ As a result, we created a patient consent form for the donors of primary cells, which we also want to present as a template for future German iGEM teams. <b>However, we want to emphasize that it is not guaranteed to be comprehensive, nor does it have any legal approval</b>. We also developed a guideline, which we present as a template, on handling primary cells to ensure not only proper technical handling but also correct ethical treatment.</p>
+ <p></p>
<div className='row align-items-center'>
<div className='col '>
<H4 text="Patient consent form"/>
- <p></p>
- <p>When working with primary cultures, it is extremely important to consider the bioethical aspects of the project. To address this, we sat down with the Ethics Officer at Bielefeld University, Dr. Berens, and discussed the matter with her. From this exchange, we gained the following insights.
- On the one hand, having a patient consent form is crucial, as it provides the donors of the primary cells with a sense of security, but more importantly, it gives them detailed and precise information about what will be done with the data, whether it be regular patient data or biomaterials. Additionally, it became clear that it is significantly easier for us to establish guidelines to follow. We decided to integrate this approach into our project.
- As a result, we created a patient consent form for the donors of primary cells, which we also want to present as a template for future German iGEM teams. <b>However, we want to emphasize that it is not guaranteed to be comprehensive, nor does it have any legal approval</b>. We also developed a guideline, which we present as a template, on handling primary cells to ensure not only proper technical handling but also correct ethical treatment.</p>
- <p></p>
<TwoLinePDF link="https://static.igem.wiki/teams/5247/pdfs/patienteneinwilligung-mustervorlage-igem-2.pdf" name="patienteneinwilligung-mustervorlage-igem-2.pdf"/>
</div>
<div className='seperator-2 col-2'>
--
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