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	<title>Medical Device Courses | Mattie718 | Mentions</title>
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				<title>Sheila Sarathy replied to the topic  &#034;Customer Needs and Design Input&#034; -</title>
				<link>https://medicaldevicecourses.com/activity/p/24148/</link>
				<pubDate>Mon, 06 Dec 2021 15:39:16 -0500</pubDate>

									<content:encoded><![CDATA[<p><a href='https://medicaldevicecourses.com/members/mattie718/' rel="nofollow ugc">@mattie718</a> I would have to agree with you in the sense that the Design Input Document (DID) and Design Specification Document (DSD) are similar documents. But I do think that the DID is most vital because the writer who composed&#8230; &nbsp; <a href="https://medicaldevicecourses.com/forums/introduction-to-design-controls/customer-needs-and-design-input/paged/3/#post-13257" rel="nofollow ugc">Read more&raquo;</a></p>
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				<title>AniketB replied to the topic  &#034;Possibility of Global Regulation of Medical Devices?&#034; -</title>
				<link>https://medicaldevicecourses.com/activity/p/17622/</link>
				<pubDate>Wed, 15 May 2019 21:41:09 -0400</pubDate>

									<content:encoded><![CDATA[<p>I don&#8217;t think the medical device community is moving towards globalization of regulatory procedures but in future, an optional global standard must exist. Each country has its own set of regulatory standards for device manufacturers, I agree with <a href='https://medicaldevicecourses.com/members/mattie718/' rel="nofollow ugc">@mattie718</a> on&#8230; &nbsp; <a href="https://medicaldevicecourses.com/community/introduction-to-project-management/possibility-of-global-regulation-of-medical-devices/#post-7294" rel="nofollow ugc">Read more&raquo;</a></p>
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				<title>AniketB replied to the topic Possibility of Global Regulation of Medical Devices? in the forum Introduction to Project Management</title>
				<link>https://medicaldevicecourses.com/activity/p/9505/</link>
				<pubDate>Sun, 10 Feb 2019 11:39:39 -0500</pubDate>

									<content:encoded><![CDATA[<p>I don&#8217;t think the medical device community is moving towards globalization of regulatory procedures but in future, an optional global standard must exist.<br />
Each country has its own set of regulatory standards for device manufacturers, I agree with <a href='https://medicaldevicecourses.com/members/mattie718/' rel="nofollow ugc">@mattie718</a> on the point that globalization of regulatory standards will have strict requirements of&hellip;<span class="activity-read-more" id="activity-read-more-9505"><a href="https://medicaldevicecourses.com/activity/p/9505/" rel="nofollow ugc">[Read more]</a></span></p>
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