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	<title>Audits &#8211; Eisner Safety Consultants</title>
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	<link>https://eisnersafety.com</link>
	<description>Regulatory &#38; Safety Experts for Global Medical Device Approvals</description>
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	<title>Audits &#8211; Eisner Safety Consultants</title>
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		<title>What Do You Need to Know About Remote Audits?</title>
		<link>https://eisnersafety.com/2020/05/29/remote-medical-device-audits/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=remote-medical-device-audits</link>
		
		<dc:creator><![CDATA[leoeisner]]></dc:creator>
		<pubDate>Fri, 29 May 2020 06:20:16 +0000</pubDate>
				<category><![CDATA[Auditing]]></category>
		<category><![CDATA[COVID]]></category>
		<category><![CDATA[May 2020]]></category>
		<category><![CDATA[Remote Auditing]]></category>
		<category><![CDATA[audit]]></category>
		<category><![CDATA[Audits]]></category>
		<category><![CDATA[remote audit]]></category>
		<category><![CDATA[Remote Audits]]></category>
		<guid isPermaLink="false">https://eisnersafety.com/?p=6701</guid>

					<description><![CDATA[Are you falling behind on your internal audit or supplier audit plans due to COVID-19, other emergency situations, sickness, travel restrictions, time constraints?&#160; It really doesn’t matter the reason why you can rely on external resources to support your audits]]></description>
										<content:encoded><![CDATA[
<figure class="wp-block-image size-large"><img fetchpriority="high" decoding="async" width="705" height="1024" src="https://eisnersafety.com/eisnersafetycom/wp-content/uploads/2020/05/Handdrawnlightbul-705x1024.png" alt="" class="wp-image-6711" srcset="https://eisnersafety.com/wp-content/uploads/2020/05/Handdrawnlightbul-705x1024.png 705w, https://eisnersafety.com/wp-content/uploads/2020/05/Handdrawnlightbul-600x871.png 600w, https://eisnersafety.com/wp-content/uploads/2020/05/Handdrawnlightbul-207x300.png 207w, https://eisnersafety.com/wp-content/uploads/2020/05/Handdrawnlightbul-768x1115.png 768w, https://eisnersafety.com/wp-content/uploads/2020/05/Handdrawnlightbul.png 858w" sizes="(max-width: 705px) 100vw, 705px" /></figure>



<p>Are you falling behind on your internal audit or supplier
audit plans due to COVID-19, other emergency situations, sickness, travel
restrictions, time constraints?&nbsp; It
really doesn’t matter the reason why you can rely on external resources to
support your audits plans for internal and supplier audits to keep your QMS on
track.</p>



<p>Some items to consider for a remote audit that we like to
discuss with our clients up front:</p>



<ul class="wp-block-list"><li>Are you able to access RA/QA documents &amp; records if you are working from home?</li><li>Are your RA/QA documents &amp; records maintained digitally or can they be pdf’ed? </li><li>Are you able to share RA/QA documents &amp; records during the remote audit live (scroll through on-screen) or share them thru tools like DropBox, Google Drive, or similar so the auditor(s) can review during the audit?</li><li>How do you guarantee the documents you share with the audit team are returned or destroyed?</li><li>What are your confidentiality policies and how will that limit your ability to share documents?&nbsp; </li><li>What about if your auditor is a foreign national and you have national security requirements you need to follow?</li><li>Coordination of a test run of the selected technology to use for the remote audit to make sure work through issues upfront and deal with bandwidth, contingency planning, live document review, &amp; document sharing.</li><li>This list is going to vary depending on your specific circumstances so have an honest discussion with the auditor upfront and during audit planning to make sure the appropriate preparations and contingency plans are considered.</li></ul>



<p>ISO 19011:2018 allows for remote auditing with the use of
technology such as Webex, Zoom, Skype, or other video conferencing services
along with document sharing services such as DropBox, Google Drive, Box, and
more.&nbsp; The goal of the remote or the on-site
audit is the same to verify objective evidence.</p>



<p>Your auditor should be flexible to work with you for what tech works best for your organization.&nbsp; Work with the auditor to determine ground rules upfront and ask your auditor to review the following checklist of items well before the audit:</p>



<ul class="wp-block-list"><li><strong>Audit Plan:&nbsp;&nbsp;</strong>Ask your auditor for an audit plan at least several weeks in advance so you can arrange personnel off-site &amp; on-site.&nbsp; Will all personnel in the audit be on the same time zone and do you need break out room(s) for multiple auditors? &nbsp;Ask the lead auditor to list what generic documents they always request for all audits so you can have prepared<ul><li>Quality Manual</li></ul><ul><li>List/index of all QMS procedures/work instructions</li></ul><ul><li>Management Review procedure</li></ul><ul><li>Complaint handling procedure</li></ul><ul><li>List of complaints since the last audit</li></ul><ul><li>CAPA procedure</li></ul><ul><li>List of CAPA open/close since the last audit</li></ul><ul><li>Internal audit schedule</li></ul></li><li><strong>Sampling Records:&nbsp;&nbsp;</strong>The auditor will need to sample records like in any on-site audit, so query them how this will be done, which types of records will be needed, and in what format the records should be (example: screenshots of folders showing record files, live shots of records, discuss what works for your existing tech).&nbsp;&nbsp;&nbsp;&nbsp; </li><li><strong>Sharing of Files:</strong>&nbsp;&nbsp;You should request the auditor be flexible enough to use the technology that works best for your organization unless the auditor is physically unable to use the specific technology.</li><li><strong>Contingency Planning:&nbsp; </strong>What happens if an auditor or auditee gets disconnected or if there are some technical issues?&nbsp; Come to an agreement on what should be done.</li><li>Agreement of Confidentiality:&nbsp;&nbsp;How will the documents you share with the auditor be accessed, saved, and discarded after the audit.&nbsp; See the fourth bullet in the above section.</li><li>Break Times:&nbsp;&nbsp;An 8-hour remote audit is a long workday and maybe too long of a workday.&nbsp; When doing a couple of remote audits of more than 2 days long it was noted that it is beneficial for all to shorten the remote audit days to less than 7 hours of audit time.&nbsp; Also, it is critical to agree on break times including lunch breaks, short stretch breaks, and if other breaks may be needed.</li><li><strong>Test run:&nbsp;&nbsp;</strong>Conduct a test run with the auditor(s) and your team (at least some on-site &amp; off-site members) to test-drive the technology about a week prior to the audit to ensure there are no issues with internet, audio, video, document viewing/displaying, transfer of documents, sharing of files, browser compatibility, headsets, contingency planning, etc.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp; </li><li><strong>Opening &amp; Closing Meetings:&nbsp;&nbsp;</strong>Will you have all your personnel in one place, or will they be scattered off-site and on-site? If you need to pull together your personnel using an online platform such as Webex, Zoom, or similar. &nbsp;You’ll want to do a short 5 – 10 minute test run to make sure everyone can call in an make the technology works.&nbsp; You may want to test it with the auditor to make sure all parties are able to make it work.</li></ul>



<p>This is the time for you to review your internal audit and supplier audit schedules.&nbsp; We are able to support these with a <a href="https://eisnersafety.com/resources/remote-audits/">remote audit</a> to help you keep on track and on schedule.</p>



<p>Feel free to contact us to discuss your needs. Contact Leo Eisner to help you thru this process by&nbsp;<a href="https://www.eisnersafety.com/eisnersafetycom/Schedule-Call/">scheduling a call</a>&nbsp;with Leo.</p>
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		<item>
		<title>Medical Device Audit Training Opportunities</title>
		<link>https://eisnersafety.com/2013/01/31/medical-device-audit-training-opportunities/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=medical-device-audit-training-opportunities</link>
		
		<dc:creator><![CDATA[leoeisner]]></dc:creator>
		<pubDate>Thu, 31 Jan 2013 04:14:51 +0000</pubDate>
				<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[audio seminar]]></category>
		<category><![CDATA[audit practices]]></category>
		<category><![CDATA[audit program]]></category>
		<category><![CDATA[Audit Program Planning]]></category>
		<category><![CDATA[audit training]]></category>
		<category><![CDATA[Audits]]></category>
		<category><![CDATA[best practices]]></category>
		<category><![CDATA[ESCNews]]></category>
		<category><![CDATA[free webinar]]></category>
		<category><![CDATA[FX Conferences]]></category>
		<category><![CDATA[ISO 13485]]></category>
		<category><![CDATA[ISO 14971]]></category>
		<category><![CDATA[Medical]]></category>
		<category><![CDATA[Medical Device]]></category>
		<category><![CDATA[Medical Device Auditing]]></category>
		<category><![CDATA[Medical Device Industry]]></category>
		<category><![CDATA[Medical Device Quality]]></category>
		<category><![CDATA[Medical Device Quality System]]></category>
		<category><![CDATA[Medical Device Regulatory]]></category>
		<category><![CDATA[Medical Devices]]></category>
		<category><![CDATA[Process Approach Auditing]]></category>
		<category><![CDATA[Quality Systems]]></category>
		<category><![CDATA[Training]]></category>
		<category><![CDATA[Turtle Diagrams]]></category>
		<guid isPermaLink="false">http://www.eisnersafety.com/eisnersafetycom/?p=3081</guid>

					<description><![CDATA[Rob Packard &#38; Brigid Glass have a couple opportunities for you to learn about different aspects of medical device auditing.  These offerings are in February &#38; April 2013 and range from a 1 hour audio conference, to a free webinar,]]></description>
										<content:encoded><![CDATA[<p><span style="font-family: arial, helvetica, sans-serif; font-size: small;">Rob Packard &amp; Brigid Glass have a couple opportunities for you to learn about different aspects of medical device auditing.  These offerings are in February &amp; April 2013 and range from a 1 hour audio conference, to a free webinar, to a small face to face training.</span></p>
<p><span style="font-size: small; font-family: arial, helvetica, sans-serif;"><span id="more-3081"></span></span></p>
<p><span style="font-size: small; font-family: arial, helvetica, sans-serif;">Joe Hage (<strong><a href="http://www.medicalmarcom.com/" target="_blank" rel="noopener noreferrer">www.medicalmarcom.com</a></strong>) will be offering a free webinar, taught by Rob Packard and Brigid Glass, on the &#8220;Best Practices in Medical Device Auditing&#8221;. If you want to be part of this I suggest you click <strong><a href="http://www.linkedin.com/redirect?url=http%3A%2F%2Fmedgroup%2Ebiz%2Fbest-audits&amp;urlhash=fT-C&amp;_t=tracking_anet" target="_blank" rel="noopener noreferrer">http://medgroup.biz/best-audits</a></strong> right now to register, because 1,000 seats is the maximum available and 250 people signed up in the first 24 hours, about a day ago.</span></p>
<p><span style="font-size: small; font-family: arial, helvetica, sans-serif;"> The free webinar, scheduled for Wednesday, February 13<sup>th</sup>, 3 &#8211; 4pm (PST) or 6 &#8211; 7pm (EST), </span><span style="font-family: arial, helvetica, sans-serif; font-size: small;">will include 10 minutes on the topic of Turtle Diagrams, a 15 minute video by Brigid Glass about audit program planning, and Rob will close with about 15 minutes explaining how the topics Brigid mentioned can be applied to planning an audit. The 10 minutes Rob will spend on the topic of Turtle Diagrams is not really long enough to cover the use of the process approach in detail.  </span></p>
<p><span style="font-family: arial, helvetica, sans-serif; font-size: small;">Rob mentioned to me that he is also teaching a 1-hour audio seminar through FX Conferences on Tuesday, February 19th, 8:30am to 9:30am (PST) or 11:30am to 12:30pm (EST). That audio seminar will be specific to the topic of Turtle Diagrams and the Process Approach. </span><strong><a style="font-family: arial, helvetica, sans-serif; font-size: small;" href="http://www.fxconferences.com/Adding-Value-to-Audits-Using-the-Process-Approach-P1170.aspx" target="_blank" rel="noopener noreferrer">http://www.fxconferences.com/Adding-Value-to-Audits-Using-the-Process-Approach-P1170.aspx</a></strong></p>
<p><span style="font-size: small; font-family: arial, helvetica, sans-serif;"> Also, check out <strong><a href="http://www.linkedin.com/redirect?url=http%3A%2F%2FMedicalDeviceAcademy%2Ecom&amp;urlhash=lFK9&amp;_t=tracking_anet" target="_blank" rel="noopener noreferrer">http://MedicalDeviceAcademy.com</a></strong>. Rob and Brigid will be teaching a live, two-day course on Best Audit Practices in April. Only 60 seats (20 per city: San Diego, Orlando, Las Vegas).</span></p>
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