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	<title>Medical Device Courses | Ahmed Elmonier | Mentions</title>
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				<title>31470977 replied to the topic  &#034;The importance of design changes and documentation&#034; -</title>
				<link>https://medicaldevicecourses.com/activity/p/60097/</link>
				<pubDate>Mon, 02 Nov 2026 04:44:03 -0500</pubDate>

									<content:encoded><![CDATA[<p><a href='https://medicaldevicecourses.com/members/ahmed-elmonier/' rel="nofollow ugc">@ahmed-elmonier</a> I feel like sometimes one can get away with not involving manufacturing until the later stages of medical device development, but I also feel like they can offer firsthand experience in medical device production. They could help identify practical&#8230; &nbsp; <a href="https://medicaldevicecourses.com/forums/introduction-to-design-controls/the-importance-of-design-changes-and-documentation/#post-24576" rel="nofollow ugc">Read more&raquo;</a></p>
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				<title>aca replied to the topic  &#034;Verification vs. validation in medical device development&#034; -</title>
				<link>https://medicaldevicecourses.com/activity/p/60092/</link>
				<pubDate>Mon, 02 Nov 2026 03:04:30 -0500</pubDate>

									<content:encoded><![CDATA[<p><a href='https://medicaldevicecourses.com/members/ahmed-elmonier/' rel="nofollow ugc">@ahmed-elmonier</a> In cases where a medical device passes verification but fails validation, then the first step should be determining if the issue is the design itself, the process, or the original requirements. It is important to understand that human error&#8230; &nbsp; <a href="https://medicaldevicecourses.com/forums/introduction-to-design-controls/verification-vs-validation-in-medical-device-development/#post-24571" rel="nofollow ugc">Read more&raquo;</a></p>
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				<title>enzo.1216 replied to the topic  &#034;Understanding Customer Needs in Medical Device Marketing&#034; -</title>
				<link>https://medicaldevicecourses.com/activity/p/59679/</link>
				<pubDate>Sun, 25 Oct 2026 23:14:33 -0400</pubDate>

									<content:encoded><![CDATA[<p><a href='https://medicaldevicecourses.com/members/ahmed-elmonier/' rel="nofollow ugc">@ahmed-elmonier</a> I agree that asking people what they want isn’t always enough, and your manufacturing example makes the point well. I think companies should do both, but I’d lean toward observation as the better way to find problems and use&#8230; &nbsp; <a href="https://medicaldevicecourses.com/forums/marketing-and-sales/understanding-customer-needs-in-medical-device-marketing/#post-24477" rel="nofollow ugc">Read more&raquo;</a></p>
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				<title>enzo.1216 replied to the topic  &#034;Is the Best Medical Device Always the Best Selling Product ?&#034; -</title>
				<link>https://medicaldevicecourses.com/activity/p/59678/</link>
				<pubDate>Sun, 25 Oct 2026 23:11:27 -0400</pubDate>

									<content:encoded><![CDATA[<p><a href='https://medicaldevicecourses.com/members/ahmed-elmonier/' rel="nofollow ugc">@ahmed-elmonier</a> I agree that performance matters more over time, and I like your point that marketing doesn’t stop once the product is sold. I think a strong marketing strategy can carry a company for a while, but I don’t think&#8230; &nbsp; <a href="https://medicaldevicecourses.com/forums/marketing-and-sales/is-the-best-medical-device-always-the-best-selling-product/#post-24476" rel="nofollow ugc">Read more&raquo;</a></p>
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				<title>enzo.1216 replied to the topic  &#034;Who Should Be Responsible for Quality: Engineers or Dedicated QA/QC Teams?&#034; -</title>
				<link>https://medicaldevicecourses.com/activity/p/59670/</link>
				<pubDate>Sun, 25 Oct 2026 21:59:32 -0400</pubDate>

									<content:encoded><![CDATA[<p><a href='https://medicaldevicecourses.com/members/ahmed-elmonier/' rel="nofollow ugc">@ahmed-elmonier</a> I agree with your point about separating who owns quality from who has final authority, and I think that answers your question. Yes, I think employees would take quality less seriously if they saw it as only the QA/QC&#8230; &nbsp; <a href="https://medicaldevicecourses.com/forums/quality-control-and-quality-assurance/who-should-be-responsible-for-quality-engineers-or-dedicated-qa-qc-teams/#post-24469" rel="nofollow ugc">Read more&raquo;</a></p>
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				<title>aca replied to the topic  &#034;When Does a Surgeon Become a Brand Ambassador Ethically?&#034; -</title>
				<link>https://medicaldevicecourses.com/activity/p/59128/</link>
				<pubDate>Mon, 19 Oct 2026 00:10:40 -0400</pubDate>

									<content:encoded><![CDATA[<p><a href='https://medicaldevicecourses.com/members/ahmed-elmonier/' rel="nofollow ugc">@ahmed-elmonier</a> Disclosure of finances is important, but I don&#8217;t think it&#8217;s enough by itself. Even if the surgeon is completely honest about the financial relationship with a company, the relationship will always influence how they will view the medical device,&#8230; &nbsp; <a href="https://medicaldevicecourses.com/forums/marketing-and-sales/when-does-a-surgeon-become-a-brand-ambassador-ethically/#post-24402" rel="nofollow ugc">Read more&raquo;</a></p>
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				<title>dcapera replied to the topic  &#034;Can Product Claims Make Things More Complicated?&#034; -</title>
				<link>https://medicaldevicecourses.com/activity/p/58780/</link>
				<pubDate>Sun, 27 Sep 2026 23:46:27 -0400</pubDate>

									<content:encoded><![CDATA[<p><a href='https://medicaldevicecourses.com/members/ahmed-elmonier/' rel="nofollow ugc">@Ahmed-elmonier</a>, good point about claims changing the pathway. It connects to what we talked about with the 510(k) process. To get cleared, a new device has to be shown to be similar to a device already on the market, and&#8230; &nbsp; <a href="https://medicaldevicecourses.com/forums/regulatory-basics-for-medical-devices/can-product-claims-make-things-more-complicated/#post-24195" rel="nofollow ugc">Read more&raquo;</a></p>
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				<title>aca replied to the topic  &#034;Regulatory Classification of Novel Devices&#034; -</title>
				<link>https://medicaldevicecourses.com/activity/p/58776/</link>
				<pubDate>Sun, 27 Sep 2026 22:58:12 -0400</pubDate>

									<content:encoded><![CDATA[<p><a href='https://medicaldevicecourses.com/members/ahmed-elmonier/' rel="nofollow ugc">@ahmed-elmonier</a> The FDA should definitely consider the specific kinds of risks a potential new device can pose when deciding a new pathway. Certain risks can be easily detected and controlled compared to other risks. For instance, if there is a&#8230; &nbsp; <a href="https://medicaldevicecourses.com/forums/regulatory-basics-for-medical-devices/regulatory-classification-of-novel-devices/#post-24192" rel="nofollow ugc">Read more&raquo;</a></p>
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				<title>James Olson replied to the topic  &#034;From Pre-Clinical Research to Human Trials: When Is the Evidence Enough ?&#034; -</title>
				<link>https://medicaldevicecourses.com/activity/p/57969/</link>
				<pubDate>Sun, 20 Sep 2026 23:06:41 -0400</pubDate>

									<content:encoded><![CDATA[<p><a href='https://medicaldevicecourses.com/members/ahmed-elmonier/' rel="nofollow ugc">@ahmed-elmonier</a> I would definitely say the level of evidence needed before moving on should depend on the details of the condition. For example, if a new technology is being developed to potentially reduce the deterioration of a degenerative muscular disease,&#8230; &nbsp; <a href="https://medicaldevicecourses.com/forums/pre-clinical-device-development/from-pre-clinical-research-to-human-trials-when-is-the-evidence-enough/#post-24096" rel="nofollow ugc">Read more&raquo;</a></p>
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				<title>James Olson replied to the topic  &#034;Deciding How to Perform Research in Industry&#034; -</title>
				<link>https://medicaldevicecourses.com/activity/p/57963/</link>
				<pubDate>Sun, 20 Sep 2026 22:29:10 -0400</pubDate>

									<content:encoded><![CDATA[<p><a href='https://medicaldevicecourses.com/members/ahmed-elmonier/' rel="nofollow ugc">@ahmed-elmonier</a> I wouldn&#8217;t use an outside lab for industry for the reason you mentioned, the reduced control and monitoring over the lab. For projects to maintain consistent deadlines, adding a non-affiliated entity to the project has increased potential for miscommunication&#8230; &nbsp; <a href="https://medicaldevicecourses.com/forums/pre-clinical-device-development/deciding-how-to-perform-research-in-industry/#post-24095" rel="nofollow ugc">Read more&raquo;</a></p>
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				<title>enzo.1216 replied to the topic  &#034;Pressure vs. Safety: A Project Manager’s Toughest Decision&#034; -</title>
				<link>https://medicaldevicecourses.com/activity/p/57353/</link>
				<pubDate>Mon, 14 Sep 2026 23:58:59 -0400</pubDate>

									<content:encoded><![CDATA[<p><a href='https://medicaldevicecourses.com/members/ahmed-elmonier/' rel="nofollow ugc">@ahmed-elmonier</a> I agree with your point that a safety concern does not always mean the entire project needs to stop because a safety concern does not necessarily affect every part of the project. I believe that the project manager should&#8230; &nbsp; <a href="https://medicaldevicecourses.com/forums/intro-to-project-management/pressure-vs-safety-a-project-managers-toughest-decision/#post-24049" rel="nofollow ugc">Read more&raquo;</a></p>
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