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	<title>Standards db &#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>Standards Reconnaissance Subscription Service Coming Soon</title>
		<link>https://eisnersafety.com/2015/08/31/standards-reconnaissance-subscription-service-coming-soon/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=standards-reconnaissance-subscription-service-coming-soon</link>
		
		<dc:creator><![CDATA[leoeisner]]></dc:creator>
		<pubDate>Mon, 31 Aug 2015 20:16:28 +0000</pubDate>
				<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[510(k)]]></category>
		<category><![CDATA[60601 series]]></category>
		<category><![CDATA[60601-1]]></category>
		<category><![CDATA[60601-1 3rd ed.]]></category>
		<category><![CDATA[AAMI]]></category>
		<category><![CDATA[AAMI ES60601-1]]></category>
		<category><![CDATA[Active Assisted Living]]></category>
		<category><![CDATA[Active Implantable Medical Devices Directive]]></category>
		<category><![CDATA[AIMDD]]></category>
		<category><![CDATA[ANSI/AAMI ES60601-1]]></category>
		<category><![CDATA[CDRH]]></category>
		<category><![CDATA[CENELEC]]></category>
		<category><![CDATA[Collateral Standard]]></category>
		<category><![CDATA[EN60601]]></category>
		<category><![CDATA[EN60601-1]]></category>
		<category><![CDATA[ESCNews]]></category>
		<category><![CDATA[EU]]></category>
		<category><![CDATA[European Commission]]></category>
		<category><![CDATA[FDA]]></category>
		<category><![CDATA[FDA Guidance]]></category>
		<category><![CDATA[Home Healthcare Environments]]></category>
		<category><![CDATA[Home Use]]></category>
		<category><![CDATA[Home Use Environment]]></category>
		<category><![CDATA[Home Use Med Dvcs]]></category>
		<category><![CDATA[IEC]]></category>
		<category><![CDATA[IEC 60601-1]]></category>
		<category><![CDATA[IEC60601-1]]></category>
		<category><![CDATA[IEC60601-1 3rd ed.]]></category>
		<category><![CDATA[IEC60601-1-11]]></category>
		<category><![CDATA[ISO]]></category>
		<category><![CDATA[MDD]]></category>
		<category><![CDATA[MDD Amendment]]></category>
		<category><![CDATA[Medical]]></category>
		<category><![CDATA[Medical Device]]></category>
		<category><![CDATA[Medical Device Directive]]></category>
		<category><![CDATA[Medical Device Industry]]></category>
		<category><![CDATA[medical device regulators]]></category>
		<category><![CDATA[Medical Device Regulatory]]></category>
		<category><![CDATA[Medical Devices]]></category>
		<category><![CDATA[Standards]]></category>
		<category><![CDATA[Standards database]]></category>
		<category><![CDATA[Standards db]]></category>
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					<description><![CDATA[Does your Medical Device Regulator or your Quality System require that you maintain a list of applicable standards to meet these requirements for your product lines?  How much time does it take to put this list together and how much]]></description>
										<content:encoded><![CDATA[<p><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"><img fetchpriority="high" decoding="async" class="alignleft size-medium wp-image-4348" src="http://www.eisnersafety.com/wp-content/uploads/2015/08/Stack-of-books-300x300.png" alt="Stack of books" width="300" height="300" />Does your Medical Device Regulator or your Quality System require that you maintain a list of applicable standards to meet these requirements for your product lines?  How much time does it take to put this list together and how much effort does it take to keep the list updated? If this is a struggle for your organization to keep up with all the different data sources we have the solution for you at a reasonable price. A Standards Reconnaissance Subscription Service to help medical electrical device manufacturers keep up to date on all the changes that occur for these documents so you are prepared for future changes well ahead of the norm and you are able to stay up to date on your list of standards. The focus of this service will be on the documents for <strong><u>medical electrical equipment &amp; systems</u></strong> (MEE&amp;S = IEC TC 62, SC 62A &#8211; 62D) and <strong><u>home use medical electrical equipment &amp; systems</u></strong><u> (Home Use MEE&amp;S = IEC Active Assisted Living System Committee (IEC AAL SyC) and any other Home Use medical electrical equipment documents from the IEC TC 62, SC 62A – 62D including IEC 60601-1-11 Home Use Environment)</u>.</span></p>
<p><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">We plan to go live with the db by the end of Sept 2015.</span></p>
<p><a href="#RSVP"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"><strong><u>Please reserve your spot</u></strong> by September 28, 2015 for this db subscription service.</span></a></p>
<p><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Some of the features will include [For Paid Subscribers unless noted otherwise]:</span></p>
<ul>
<li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Notification e-mails when changes occur (i.e. Change in transition information from FDA for a standard) and new records are entered into the db.</span></li>
<li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Receive either 2 or 4 reports per year (depending on Subscription level) summarizing:</span>
<ul>
<li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">key issues of that report cycle for MEE&amp;S or home Use MEE&amp;S,</span></li>
<li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">estimated timeline for the publication of draft standards &amp; other relevant documents of significance, and</span></li>
<li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">full listing of all the documents in your part of the db with status information.</span></li>
</ul>
</li>
<li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Access to our searchable db (depending on Subscription level access to the either the MEE&amp;S or Home Use MEE&amp;S part of the db or the whole db) on our dedicated db website if you are a paid subscriber. [Limited access for free level of service with 10 – 15 standards (pre-defined)]</span></li>
<li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Print out db search results the way you want them</span></li>
<li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Export db search results for your use (limited by the terms &amp; conditions of the db)</span></li>
</ul>
<p><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">There are several parts of this db [For Paid Subscribers unless noted otherwise]:</span></p>
<ul>
<li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Standards db &#8211; including information on the standards, technical reports, technical specifications, and publicly available specifications that are active or current, in draft or development which would include voting level documents such as New Work Proposals, Committee Drafts, etc., and withdrawn documents (The previous version of the active standard).</span></li>
<li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">List of standards publishers &amp; associated country (this will cover 50+ countries) [includes free service level],</span></li>
<li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">List of Medical Device Regulators with their websites, if available, for a selection of countries including all the of EU &amp; EFTA countries.  We plan to expand this to include all countries in the world by the end of Stage 2 (below),</span></li>
<li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Guidance Documents – Guidance documents that the regulatory bodies use for their national regulatory systems. Like for the US, Canada, &amp; Europe. They will be added sometime after going live by end of stage 2 or 3 (see below).</span></li>
</ul>
<p><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Once the db goes live you can check out how the db works by accessing the free level of service to view a few examples of current standards (about 10 to 15). With the free service level you will be able to use most of the db features set other than obtaining reports, the update notification service, but you will not have access to List of Medical Device Regulators db of Guidance documents db.</span></p>
<p><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Pricing starts at only:</span></p>
<ul>
<li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">$4,500/year for Base Entry Subscription (2 reports per year and select either MEE&amp;S or Home Use MEE&amp;S part of db),</span></li>
<li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">$6,500/year for Mid-Level Subscription (4 reports per year and full access to db), or</span></li>
<li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">$9,000/year &amp; up for Premium Subscription (2 personalized reports for your company’s needs based on conversations with Leo Eisner, 2 reports per year from the Premium Subscription level, and full access to db)</span><br />
<span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">All payments to be paid in US$ only.</span></li>
</ul>
<p><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">We plan to go live with the db by the end of Sept 2015. Since we will be releasing the db in stages the early adopters will get a discount (20%) for the first annual subscription cycle and additionally we will throw in extra months to your subscription commensurate with how early you subscribe.  The earlier you subscribe the more free months will be added to your first yearly subscription for no additional charge.</span><br />
<a name="RSVP"></a><br />
<span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"><strong><u>Please reserve your spot</u></strong> by September 28, 2015 for this db subscription service and to <strong><u>guarantee a discounted first year price and to obtain extra months added for free</u></strong>. To reserve your spot for the Base entry or the Mid-Level Subscriptions please arrange a $750.00 (US$) deposit and for the Premium Subscriptions please arrange a $1,500.00 (US$) deposit. Contact us to arrange for deposit.</span></p>
<p><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">There will be a couple stages for the release of information for the db.  We plan on continual updates over time to provide a really valuable resource and continually make it better. The first stage will be complete prior to the official release of the db which will include all the updated information for the IEC based MEE&amp;S &amp; Home Use MEE&amp;S documents including updates on the small number of joint IEC/ISO documents.  Stage 2 will be initiated just before the release of the db, which will include updates for the US, EU, and Canadian versions of the IEC &amp; IEC/ISO MEE&amp;S and Home Use MEE&amp;S documents and IEC/ISO joint documents. We plan to have stage 2 completed around Jan 2016.  Stage 3 will include updated information adding in the supporting medical device (non-medical-electrical) documents you need for your regulatory submissions such as ISO 10993 series of standards, ISO 15223-1, etc.  This stage will initiate with the non-medical-electrical standards for IEC and ISO and in the future we will add other Standards Developers.  We expect to start on stage 3 around Jan 2016 and have not yet scheduled it’s completion.</span></p>
<p><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Please contact Leo Eisner to find out more details about this db. He can be reached by e-mail or phone at <a href="mailto:Le&#111;&#64;E&#105;sn&#101;rS&#97;f&#101;&#116;&#121;.&#99;o&#109;">&#76;&#101;&#111;&#64;&#69;is&#110;&#101;&#114;Saf&#101;&#116;&#121;.c&#111;m</a> and 503-244-6151 (Office) and 503-709-8328 (Cell).</span></p>
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