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	<title>Sitrof Technologies &#187; Resources</title>
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		<title>A trusted partner through the content migration process</title>
		<link>http://sitrof.com/resources/insights/life-sciences-content-migration-part-11-compliance/</link>
		<comments>http://sitrof.com/resources/insights/life-sciences-content-migration-part-11-compliance/#comments</comments>
		<pubDate>Tue, 31 Jan 2012 21:23:28 +0000</pubDate>
		<dc:creator>Sitrof</dc:creator>
				<category><![CDATA[Insights]]></category>
		<category><![CDATA[21 CFR Part 11]]></category>
		<category><![CDATA[compliance]]></category>
		<category><![CDATA[Content migration]]></category>
		<category><![CDATA[Document Management]]></category>
		<category><![CDATA[ECM]]></category>

		<guid isPermaLink="false">http://sitrof.com/?p=3824</guid>
		<description><![CDATA[There are nearly as many reasons for life sciences companies to perform content migrations as there are life sciences companies. A merger or acquisition often necessitates the process. But it could be a lack of support for legacy systems, or the increased cost of maintaining old hardware overshadowing the cost of migration. It could simply [...]]]></description>
			<content:encoded><![CDATA[<h3>There are nearly as many reasons for life sciences companies to perform content migrations as there are life sciences companies.</h3>
<h4>A merger or acquisition often necessitates the process. But it could be a lack of support for legacy systems, or the increased cost of maintaining old hardware overshadowing the cost of migration. It could simply be the desire to switch to a less expensive document management solution.</h4>
<p>In any case, running multiple document management systems parallel to one another is not an option – such a situation is confusing to end users, resulting in a productivity drain. Plus, IT expenses skyrocket as maintenance time increases and hard costs rise.</p>
<p>Analyzing processes, planning the transition, getting buy-in from staff, implementing the changes – who can companies trust to get it done right the first time? For more than a decade, Sitrof has performed complex migrations for Fortune 100 companies, successfully migrating content from a variety of sources to different target repositories. With a special focus on life sciences companies and regulated environments (including those governed by FDA 21 CFR Part 11), Sitrof is the trusted provider for complex content migrations.</p>
<h4>The Sitrof Approach</h4>
<p>Backed by years of life sciences experience and world-class software industry partnerships, Sitrof is the industry leader in vendor-neutral system integration services.</p>
<p>No two migrations are the same. Sometimes, an off-the-shelf migration tool – like Buldoser or FME’s migration-center – can get the job done. Sometimes, a custom solution is necessary. Sitrof offers best-of-breed solutions when it comes to either approach – or a combination of the two.</p>
<p>Recently, a large generic pharmaceutical manufacturer needed to migrate a subset of documents from their legacy GxPharma solution to a FirstDoc FDQM 5.0 system. The company elected to use CSC Configuration Management Utility to perform the migration, but a unique set of complicating factors required a unique solution. The GxPharma system was running Documentum version 4.2.8, while the FDQM system was running Documentum version 6.0 SP1. Because CMU 5.0 uses DFC 6.0 SP1 and cannot connect to a 4.28 repository, Sitrof issued CMU 4.2 to perform the export while using CMU 5.0 to perform the import and post-import processing steps.</p>
<p>Essentially, if a company owns a migration utility, Sitrof can use it. If a company does not, Sitrof can custom-create a solution based on need and cost. Any migration is possible – one system to one system, one system to many systems or many systems to one system. With years of experience moving data into and out of FirstDoc, Documentum, SharePoint, FileNet and DocuShare, Sitrof has the wide-ranging expertise it takes to get the job done.</p>
<h4>The Sitrof Process</h4>
<p>Sitrof-engineered migrations begin with an in-depth discovery process. By first determining the scope of the project and the tools necessary, Sitrof can, in many cases, even <a href="http://sitrof.com/solutions/fixed-price-content-migration-from-sitrof/">offer an upfront fixed price</a>.</p>
<p>One recent merger brought together two leading life sciences companies – with five distinct document management systems between them. Sitrof identified the requirements for migrating each into the target system, and standardized naming protocols and security procedures. By the time the actual migration started, careful planning had mitigated the risk of unpleasant surprises and bottlenecks. In the end, the complex migration and validation of terabytes’ worth of regulated content proceeded smoothly.</p>
<p>Sitrof’s proven process allows it to migrate a company’s data, content and metadata, no matter how many repositories they have or need. Just as importantly, Sitrof guarantees all migrations are performed successfully through strict validation requirements. Whether it’s a large customer with a set migration methodology or a smaller client in need of consultation, Sitrof ensures FDA and EMA compliance, no matter how rigorous the regulatory requirements.</p>
<h4>Don’t go it alone</h4>
<p>Trying to complete a migration project in-house can seem attractive from a cost and effort perspective – at first. While the actual migration process – moving documents from Location X to Location Y – seems relatively straightforward, what surrounds it is not. A migration is a golden opportunity to streamline and cleanse systems of outdated and unnecessary documents and files. Without the right people, processes and methodology, businesses can struggle to fully leverage the opportunities a migration provides.</p>
<p>Whatever the reason for undergoing the process, Sitrof offers life sciences companies maximum return on their migration investment, as well as proven, trustworthy, validated solutions for all client sizes.</p>
<p><em>Dan Wheeler is a managing partner and co-founder of <a href="http://www.sitrof.com">Sitrof Technologies</a>, 700 Alexander Park, Princeton, N.J. 08540.</em></p>
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		<title>E-Document Collaboration During The Clinical Trial Process</title>
		<link>http://sitrof.com/resources/insights/e-document-collaboration-during-the-clinical-trial-process/</link>
		<comments>http://sitrof.com/resources/insights/e-document-collaboration-during-the-clinical-trial-process/#comments</comments>
		<pubDate>Tue, 27 Dec 2011 20:03:33 +0000</pubDate>
		<dc:creator>Sitrof</dc:creator>
				<category><![CDATA[Case Studies]]></category>
		<category><![CDATA[Insights]]></category>
		<category><![CDATA[Published Articles]]></category>
		<category><![CDATA[21 CFR Part 11]]></category>
		<category><![CDATA[Document Management]]></category>
		<category><![CDATA[ECM]]></category>
		<category><![CDATA[SharePoint]]></category>

		<guid isPermaLink="false">http://sitrof.com/?p=3776</guid>
		<description><![CDATA[The benefits of peer-to-peer networking over email, fax, FTP or hosted third-party services  The need for life sciences companies to collaborate with external partners, whether it’s Legal Counsel, Contract Research Organizations (CRO’s), Manufacturers or Joint Venture partners, has become a daily occurrence. Documents such as Contracts, Informed Content and Protocols require authoring, review and approval [...]]]></description>
			<content:encoded><![CDATA[<h3>The benefits of peer-to-peer networking over email, fax, FTP or hosted third-party services</h3>
<h4> The need for life sciences companies to collaborate with external partners, whether it’s Legal Counsel, Contract Research Organizations (CRO’s), Manufacturers or Joint Venture partners, has become a daily occurrence. Documents such as Contracts, Informed Content and Protocols require authoring, review and approval from individuals both inside and outside the company. This trend will continue as life sciences companies increase outsourcing efforts at the same time the amount of unstructured content generated each year skyrockets.1</h4>
<p>There are many different use cases in the clinical trial process that require the need for this type of data exchange. For example, Investigator’s Brochures (IB) are exchanged between study sponsors, investigators and Institutional Review Boards (IRB). These are not static documents thus requiring collaboration as updates are needed whenever new relevant information is found during a trial. Creating, reviewing and approving Informed Consent language requires a collaborative process that involves input from investigators and IRBs. Investigators are required to complete a Form 1572 along with a summary of their qualifications (typically a CV) and provide it to the sponsor before participating in a trial.</p>
<p>Documents such as these are vital to the safety and efficient operation of a clinical study. Failure to have a reliable, consistent and compliant approach to document exchange and collaboration with relevant parties can result in unnecessary delays and additional costs</p>
<h4>Challenges with Common Document Sharing Methods</h4>
<p>Many CROs and life sciences companies today collaborate and exchange content either through email, fax, File Transfer Protocol (FTP) or hosted third-party solutions. Each of these methods has its disadvantages in terms of security, document versioning, cost, efficiencies and information loss.</p>
<h4>Email</h4>
<p>For example, email may be easy to use, and is by far the most widely used communication mechanism in the corporate world. However, sending attachments through email is typically not secure because most of us aren’t encrypting attachments. Attachments also cause our mailboxes to quickly exceed their quota. More troublesome is the fact that there is often confusion about which version of the attachment is the latest—a problem that is exacerbated as the number of collaborating users increases. The end result is a time-consuming, frustrating and error-prone process of manually merging multiple documents to ensure the latest edits and comments are incorporated into a single document.</p>
<h4>Fax</h4>
<p>Like email, facsimile technologies are commonplace in the workplace. Most fax solutions today convert incoming faxes to digital format and email the document to the recipient. This may be sufficient if the receiver does not need to modify the document. However, in a collaborative environment—where both the sender and receiver must author or edit the document—the resulting PDF or TIFF file is not an editable document and is unsuitable for this purpose.</p>
<h4>FTP</h4>
<p>FTP collaboration, while not as commonly used as email or fax, has a long history of providing a secure means of exchanging files. However, these solutions require more advanced technical knowledge, are cumbersome to use and typically require IT involvement to initially set up and configure permissions and access. Security aside, the lack of version management is as much a problem with FTP as it is with email.</p>
<h4>Third-Party Solutions</h4>
<p>Some hosted third-party ("on-demand") solutions solve some of the problems of email and fax by providing a common repository for all parties so there should be no question about which version of the document is the latest. Features such as document version control are useful in that you can go back to an old version of a particular document and have greater insight into how the document has changed throughout the collaborative process. However, not all on-demand solutions offer versioning features, including one of the leading solutions on the market. Some on-demand solutions do provide audit capabilities. This provides for better compliancy by tracking the user, date and time for each document change.</p>
<p>On-demand solutions have a potentially large cost downside, however. These services typically charge by the number of documents or the amount of storage space consumed. As such, they can quickly become expensive. In addition, these solutions require a username and password to connect, which is typically not synchronized with the user’s network username and password. This requires users to remember yet another username and password. This in turn leads to security and compliance issues—for example, users have been known to write passwords on a sticky note and keep it under their keyboard.</p>
<h4>Peer-to-Peer Data Sharing: The Ideal Solution</h4>
<p>The drawbacks associated with all of these methods—some of which are quite serious—has escalated the need to find a more secure, cost-effective and user-friendly way to manage documents. The solution at hand is peer-to-peer data sharing, one of the most effective content delivery methods available today. Peer-to-peer is an approach to computer networking where all computers share equivalent responsibility for processing data.</p>
<p>Of course, there is one critical consideration to make when selecting a document exchange and collaboration solution: Above all, it must be easy for the end-user to use. This speeds adoption of the new process, avoids costly upfront and ongoing training costs and eliminates the all-too-common scenario where end-users revert back to using email to share documents.</p>
<h4>Lower Cost, Improved Performance</h4>
<p>Peer-to-peer networking (also known simply as peer networking) differs from client-server networking, where certain devices have responsibility for "serving" the data and other devices consume or otherwise act as "clients" of those servers.</p>
<p>Peer networking significantly reduces technology costs for file sharing while dramatically improving the performance and scalability of the document creation, maintenance and review process. It allows organizations to seamlessly add speed and efficiency for content collaboration, while requiring no changes to the business's current technology infrastructure. This greatly improves the end-user experience and securely speeds up the process of document collaboration for both internal and external parties.</p>
<p>In a peer networking solution, desktop computers can easily be configured to allow sharing of files, printers and other resources across all connected devices, allowing data to be shared easily in both directions—whether downloads to or uploads from your computer. Peer networking can also handle a very high volume of file sharing traffic because the load is distributed across many computers.</p>
<h4>Improved Security</h4>
<p>Because trial-related documents contain proprietary information and/or sensitive patient data, improved security is a must. For example, if a CRO is working with three separate life sciences companies, it is important, from both a compliance and contractual standpoint, to have three separate workspaces to reduce the risk that a confidential document from Life Sciences Company A is not seen by Life Sciences Company B. Peer networking documents that are exchanged between any two parties are stored within their own individual workspace.</p>
<p>An effective peer network also automatically encrypts and replicates data among users, allowing every user to have constant access to the latest shared documents—even if they are not online. It is also important for the solution to encompass built-in disaster recovery by having the data stored in at least two separate locations.</p>
<h4>Accurate Version Control and Tracking</h4>
<p>Peer networking should allow CROs to track and manage documents in several ways, including version control and status change notifications via email or text. Additionally, automatic status update indicators should be displayed to alert users of new updates within the application interface. This allows for real-time interaction and updates among users, ensuring a more efficient and accurate collaboration process.</p>
<h4>Cost-Effective Infrastructure</h4>
<p>One of the most important benefits of a peer networking solution is the elimination of the storage and file-transfer costs typically associated with on-demand services. The ideal peer networking solution requires minimal end-user training and greatly reduces administration, resources and maintenance from a central IT infrastructure, lowering overall costs and accelerating the investment payback.</p>
<h4>Integration with Existing Document Management Systems</h4>
<p>An exchange and collaboration solution should allow for integration with an existing document management system. For example, take the scenario where an Investigator’s Brochures (IB) is initially created. The authoring and review should happen in a collaborative workspace but, once complete, it should be moved seamlessly into a document management system (DMS) such as Documentum or SharePoint where it can go through a formal approval process with electronic signatures. When the IB needs to be modified at a later date, a change request should be submitted, and once approved, the IB should seamlessly be copied back into the collaborative workspace. Then the IB can be modified by all relevant parties. After the IB is revised, it should be moved or published back into the DMS.</p>
<h4>Universal Platform Support</h4>
<p>As the Apple Mac is gaining popularity in the corporate world, any peer networking solution should be innately compatible with both Windows and Mac computers.</p>
<h3>Conclusion</h3>
<p>The most common methods of document sharing and collaboration in use today—predominantly email, fax and FTP—are inadequate and insecure. Expensive managed third-party solutions may also be insufficient, particularly for highly regulated life sciences needs.</p>
<p>A good peer networking solution, on the other hand, will allow life science companies and CROs to balance multiple factors such as total cost of ownership (TCO), ease of use, robust version control capabilities, auditing and integration into a true document management system. The end result: a comprehensive solution with improved workflow, 21 CFR Part 11 compliant electronic signatures, change management and records retention capabilities.</p>
<p>Life sciences companies that adopt peer networking will experience improved document exchange and collaboration processes with external business partners. This reduces risk, compliance and security issues, while at the same time promoting efficiencies and cost savings. CROs that offer robust exchange and collaboration solutions using peer networking also stand to gain a competitive advantage while providing benefit back to their life sciences customers. In turn, these customers will be able to launch products faster because the document-intensive clinical trial and submission management processes are streamlined and made more secure.</p>
<p>&nbsp;</p>
<p>1 J. Malek, Transforming Life Sciences: The Connected Life Sciences Company,</p>
<p>Cisco Internet Business Solutions Group (IBSG), July 2009</p>
<p>2 Peer-to-Peer, Harnessing the Power of Disruptive Technologies, March 2001</p>
<p>Dan Wheeler is a managing partner and co-founder of Sitrof Technologies, 700 Alexander Park, Princeton, NJ 08540</p>
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		<item>
		<title>Presenting at EMC Life Sciences Summit</title>
		<link>http://sitrof.com/resources/insights/presenting-at-emc-life-sciences-summit/</link>
		<comments>http://sitrof.com/resources/insights/presenting-at-emc-life-sciences-summit/#comments</comments>
		<pubDate>Tue, 13 Sep 2011 19:30:14 +0000</pubDate>
		<dc:creator>Sitrof</dc:creator>
				<category><![CDATA[Insights]]></category>

		<guid isPermaLink="false">http://sitrof.com/?p=3523</guid>
		<description><![CDATA[On Wednesday, Sitrof will be presenting at the EMC Life Sciences Summit. I am looking forward to connecting with colleagues at EMC and Paragon, and my topic, "Leveraging Document Management and Pharmacovigilance." The Summit is meant to take an in-depth look at how the latest technologies are being used to solve critical business issues within [...]]]></description>
			<content:encoded><![CDATA[<p>On Wednesday, Sitrof will be presenting at the EMC Life Sciences Summit. I am looking forward to connecting with colleagues at EMC and Paragon, and my topic, "Leveraging Document Management and Pharmacovigilance."</p>
<p>The Summit is meant to take an in-depth look at how the latest technologies are being used to solve critical business issues within the life sciences industry. The event, on September 14 in Basking Ridge, NJ will also cover electronic trial master files and records management in small sessions and discussions.</p>
<p>For more information on the EMC Life Sciences Summit, <a href="http://sitrof.com/resources/news/sitrof-technologies-to-present-at-emc-life-sciences-summit/" target="_blank">click here</a>.</p>
<p>&nbsp;</p>
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		<title>Sitrof Technologies Introduces Sitrof Safety Capture for Oracle Argus Safety</title>
		<link>http://sitrof.com/uncategorized/sitrof-technologies-introduces-argus-capture-powered-by-emc-inputaccel/</link>
		<comments>http://sitrof.com/uncategorized/sitrof-technologies-introduces-argus-capture-powered-by-emc-inputaccel/#comments</comments>
		<pubDate>Tue, 06 Sep 2011 18:26:40 +0000</pubDate>
		<dc:creator>Sitrof</dc:creator>
				<category><![CDATA[News]]></category>
		<category><![CDATA[Uncategorized]]></category>

		<guid isPermaLink="false">http://sitrof.com/?p=3500</guid>
		<description><![CDATA[Sitrof Technologies, a leading provider of unstructured content management solutions for the life sciences industry, announced a new product today, Sitrof Safety Capture powered by EMC InputAccel. Sitrof Safety Capture imports all adverse event (AE) source data regardless of original format-paper, digital, fax, e-fax, email (with or without attachments)-as well as voice records from call [...]]]></description>
			<content:encoded><![CDATA[<h3>Sitrof Technologies, a leading provider of unstructured content management solutions for the life sciences industry, announced a new product today, Sitrof Safety Capture powered by EMC InputAccel.</h3>
<p>Sitrof Safety Capture imports all adverse event (AE) source data regardless of original format-paper, digital, fax, e-fax, email (with or without attachments)-as well as voice records from call centers--into Oracle Argus and other adverse event/safety management systems.</p>
<p>"It has become a pharmaceutical imperative to "unlock" AE source documents for scaling global operation and managing CROs," says Bryan Reynolds, co-founder and managing partner of Sitrof. "We were able to develop a product, powered by EMC's InputAccel, that transforms unstructured AE source documentation into searchable digital records and automatically create entries in your AE system."</p>
<p>Sitrof Safety Capture improves your company's end-to-end pharmacovigilance program by providing a holistic view of product stewardship-from clinical trials through post-marketing surveillance, by automatically creating entries in the Argus Intake Worklist. From the Intake Worklist, users have the ability to create a case from the source documentation or reject the document.</p>
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		<title>Sitrof Technologies to Present at EMC Life Sciences Summit</title>
		<link>http://sitrof.com/resources/news/sitrof-technologies-to-present-at-emc-life-sciences-summit/</link>
		<comments>http://sitrof.com/resources/news/sitrof-technologies-to-present-at-emc-life-sciences-summit/#comments</comments>
		<pubDate>Fri, 26 Aug 2011 14:29:43 +0000</pubDate>
		<dc:creator>Sitrof</dc:creator>
				<category><![CDATA[News]]></category>
		<category><![CDATA[Adverse Event Reporting]]></category>
		<category><![CDATA[AE reporting]]></category>
		<category><![CDATA[EMC]]></category>
		<category><![CDATA[linkedin]]></category>
		<category><![CDATA[Oracle Argus]]></category>
		<category><![CDATA[pharmacovigilance]]></category>
		<category><![CDATA[safety systems]]></category>

		<guid isPermaLink="false">http://sitrof.com/?p=3434</guid>
		<description><![CDATA[Sitrof, a leading provider of content management solutions for the Life Sciences industry, will present “Leveraging Document Management for Safety Reporting and Pharmacovigilance” at the EMC Life Sciences Summit, September 14, Basking Ridge, NJ. At the Summit, industry experts will take an in-depth look into how the latest technologies are being used today to solve [...]]]></description>
			<content:encoded><![CDATA[<h3>Sitrof, a leading provider of content management solutions for the Life Sciences industry, will present “Leveraging Document Management for Safety Reporting and Pharmacovigilance” at the EMC Life Sciences Summit, September 14, Basking Ridge, NJ.</h3>
<p>At the Summit, industry experts will take an in-depth look into how the latest technologies are being used today to solve critical business issues within the Life Sciences industry.</p>
<p>The event will include a continental breakfast for all attendees followed by opening remarks and three breakout sessions.</p>
<ul>
<li><strong>Electronic Trial Master File</strong>: The session will focus on leveraging intelligent capture to automate the way documents and data are captured globally in an eTMF.</li>
<li><strong>Safety Reporting: </strong>Leverage intelligent document capture to improve pharmacovigilance and integrate with leading safety systems.</li>
<li><strong>Records Management:</strong> Leveraging technology to maintain critical electronic and paper based information. See how actual retention policies and procedures combine with technology to reduce the cost and risk associated with information governance.</li>
</ul>
<blockquote class="alert">
<h3><a title="REGISTER NOW" href="https://emcinformation.com/19201/REG/.ashx?reg_src=SA"><span style="text-decoration: underline;">REGISTER NOW</span></a></h3>
</blockquote>
<h3>Agenda</h3>
<table class="contact-table" border="0" cellspacing="0" cellpadding="0" width="575">
<tbody>
<tr>
<td width="25%">
<h5>Time</h5>
<p> 8:30    -   9:00<br />
 9:00    -   9:15<br />
 9:15    -  10:15<br />
10:15 - 10:30<br />
10:30 - 12:00<br />
12:00 - 1:00
</td>
<td width="75%">
<h5>Session</h5>
<p>Registration and continental breakfast<br />
EMC: Welcome and Opening Remarks<br />
Industry Trends Overviews<br />
Break<br />
Break Out Sessions<br />
Lunch &amp; Raffle drawing</td>
</tr>
</tbody>
</table>
<h3>Location</h3>
<p>The Olde Mill Inn<br />
225 Route 202<br />
Basking Ridge, NJ 07920<br />
908-221-1100</p>
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		<title>DIA 47th Annual Meeting-What we saw!</title>
		<link>http://sitrof.com/resources/insights/dia-recap/</link>
		<comments>http://sitrof.com/resources/insights/dia-recap/#comments</comments>
		<pubDate>Thu, 30 Jun 2011 13:57:16 +0000</pubDate>
		<dc:creator>Sitrof</dc:creator>
				<category><![CDATA[Insights]]></category>
		<category><![CDATA[21 CFR Part 11]]></category>
		<category><![CDATA[compliance]]></category>
		<category><![CDATA[DIA Annual Meeting]]></category>
		<category><![CDATA[linkedin]]></category>
		<category><![CDATA[Microsoft SharePoint]]></category>

		<guid isPermaLink="false">http://sitrof.com/?p=3206</guid>
		<description><![CDATA[We just arrived back from the 47th annual DIA meeting in Chicago. We spent our time meeting up with colleagues and friends, learning, and finding out what’s new in the industry. Sitrof was glad to hear that DDMAC submissions will be accepted in eCTD format by the FDA by 2012. Our product, Approve-PTS will be [...]]]></description>
			<content:encoded><![CDATA[<p>We just arrived back from the 47th annual DIA meeting in Chicago. We spent our time meeting up with colleagues and friends, learning, and finding out what’s new in the industry.</p>
<p>Sitrof was glad to hear that DDMAC submissions will be accepted in eCTD format by the FDA by 2012. Our product, <a href="http://sitrof.com/products/approve-pts/">Approve-PTS</a> will be enhanced to support this. Approve-PTS, built on Microsoft SharePoint 2010, connects outside creative agencies, marketing teams and regulatory reviewer--allowing marketing materials to get reviewed, approved and published in the most efficient manner possible.</p>
<p>Speaking of Microsoft, we saw their huge display booth along with NextDocs and Liquent – their offerings look good and traffic was high at all three booths.  We imagine booth traffic was higher for these vendors since both EMC (IIG) and CSC were not in attendance.</p>
<p>As expected, a lot of sessions and vendors were talking about the cloud.  In the content management space, companies like Box and SpringCM are gaining traction but it’s clear the life sciences industry is not ready to put their GxP related documentation in the cloud without it first being validated.  Vevva Systems is looking to change that with their <a href="http://veevasystems.com/vault/">Vault solution</a> which is a cloud enabled content management solution built from the ground up with the Life Sciences industry in mind.  It will be interesting to see how this solution can compete with traditional on-premise solutions like Documentum and SharePoint</p>
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		<title>Sitrof Technologies featured in Applied Clinical Trials cover story</title>
		<link>http://sitrof.com/resources/insights/sitrof-technologies-featured-in-applied-clinical-trials-cover-story/</link>
		<comments>http://sitrof.com/resources/insights/sitrof-technologies-featured-in-applied-clinical-trials-cover-story/#comments</comments>
		<pubDate>Mon, 20 Jun 2011 16:24:23 +0000</pubDate>
		<dc:creator>Sitrof</dc:creator>
				<category><![CDATA[Insights]]></category>
		<category><![CDATA[Published Articles]]></category>
		<category><![CDATA[21 CFR Part 11]]></category>
		<category><![CDATA[Best Practices]]></category>
		<category><![CDATA[clinical trials]]></category>
		<category><![CDATA[Document Management]]></category>
		<category><![CDATA[DocuShare Compliance Module]]></category>
		<category><![CDATA[linkedin]]></category>
		<category><![CDATA[Xerox DocuShare]]></category>

		<guid isPermaLink="false">http://sitrof.com/?p=3130</guid>
		<description><![CDATA["Innovation in Ethical Review," an article authored by Sitrof client Jennifer Sodrel, Director of Information Management at CGIRB, is featured the cover of the May issue of Applied Clinical Trials. Sodrel’s article is based on CGIRB’s transition to a fully paperless company, a process that started in mind-2008 when CGRIB teamed with Sitrof Technologies to [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://appliedclinicaltrialsonline.findpharma.com/appliedclinicaltrials/IT+Articles/Innovation-in-Ethical-Review/ArticleStandard/Article/detail/719558?contextCategoryId=43496"><img class="alignleft size-full wp-image-3131" title="Applied-Clinical-Trials" src="http://sitrof.com/wp-content/uploads/2011/06/Applied-Clinical-Trials.jpg" alt="" width="101" height="136" /></a><a href="http://appliedclinicaltrialsonline.findpharma.com/appliedclinicaltrials/IT+Articles/Innovation-in-Ethical-Review/ArticleStandard/Article/detail/719558?contextCategoryId=43496" target="_blank">"Innovation in Ethical Review,"</a> an article authored by Sitrof client Jennifer Sodrel, Director of Information Management at CGIRB, is featured the cover of the May issue of Applied Clinical Trials.</p>
<p>Sodrel’s article is based on CGIRB’s transition to a fully paperless company, a process that started in mind-2008 when CGRIB teamed with Sitrof Technologies to install the Xerox DocuShare software and the <a title="DocuShare Compliance Module" href="http://sitrof.com/products/docushare-compliance-module/">Sitrof Compliance Module</a> for DocuShare. DocuShare was first configured to mange CGRIB’s non-regulated documents, such as vacation requests, business development information, training information, PowerPoint presentations, spread sheets, status reports, RFI’s and contracts. After giving the staff time to become familiar with DocuShare, Sitrof installed its compliance module a year later. These systems help to automate the workflow and decision process and improve efficiencies and customer service.</p>
<p>CGRIB was able to transform from a heavily paper-centered company into a completely digital, paperless organization in less than two years. Going paperless enabled CGIRB to become more efficient in all areas, with the added bonus of becoming more environmentally friendly. Sodrel encourages paperless transitions in order to help an IRB quickly collaborate, share documents, and review protocols.</p>
<p><a href="http://appliedclinicaltrialsonline.findpharma.com/appliedclinicaltrials/IT+Articles/Innovation-in-Ethical-Review/ArticleStandard/Article/detail/719558?contextCategoryId=43496" target="_blank">Click here</a> to read the full article.</p>
<p>&nbsp;</p>
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		<title>AIIM Garden State event</title>
		<link>http://sitrof.com/resources/insights/aiim-garden-state-event/</link>
		<comments>http://sitrof.com/resources/insights/aiim-garden-state-event/#comments</comments>
		<pubDate>Fri, 13 May 2011 15:07:21 +0000</pubDate>
		<dc:creator>Sitrof</dc:creator>
				<category><![CDATA[Awards and Speaking]]></category>
		<category><![CDATA[Insights]]></category>

		<guid isPermaLink="false">http://sitrof.com/?p=2925</guid>
		<description><![CDATA[Last night I spoke on a panel at the AIIM Garden State Chapter event. The topic was, “Moving from paper to an electronic environment – what does it take?” There was a great turnout at the event, and I was excited to delve into this important, but sometimes misunderstood, topic. The session started off with [...]]]></description>
			<content:encoded><![CDATA[<p>Last night I spoke on a panel at the <a href="http://www.aiim.org/chapters/chapterhome.aspx?chapterid=15" target="_blank">AIIM Garden State Chapter</a> event. The topic was, “Moving from paper to an electronic environment – what does it take?” There was a great turnout at the event, and I was excited to delve into this important, but sometimes misunderstood, topic.</p>
<p>The session started off with questions raised about the constraints of capture, there seemed to be a high barrier to entry for organizations looking to digitize their essential documents and processes.  To break through the barrier, training and education must be part of the organization. A phased approach is always recommended to optimize success.</p>
<p>I enjoyed the question and answer format of this event. The audience had many questions about finding content - I explained the Sitrof core belief of finding content based on how it’s been indexed. Indexing typically varies from over a hundred fields to a just few fields, but the general rule of thumb is 5 fields.</p>
<p>It is important to classify content and more important to OCR the document so that we enable the powerful search engines to find content. This led to more questions about search. I discussed Recommind and other technologies available which are built on the search engine and are effective in finding content such as contracts and invoices by setting up rules.</p>
<p>Once the audience released how I emphasized how key indexing is to the success of the project, and I conveyed this to the audience. Questions then shifted to how better to streamline indexing - I talked about getting the business process in place by understanding the business first and then finding a solution.</p>
<p>The final area of discussion was e-signatures. I explained the different types of signatures that exist and products such as DocuSign and CoSign. We also discussed the need for a regulatory body to standardize the signature for consistency across the board.</p>
<p>The panel agreed that because of the generation gap that paper still plays a major role in our business. As the younger generation matures, paper will continue to slowly disappear. The panel also agreed that it will take 2-3 decades for a paperless world to become a reality.</p>
<p>Thank you to the AIIM Garden State Chapter for asking me to be a part of this event. I really enjoyed it and it was great to meet everyone there.</p>
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		<title>Sitrof introduces Fixed-Price Migration</title>
		<link>http://sitrof.com/resources/news/sitrof-introduces-fixed-price-migration/</link>
		<comments>http://sitrof.com/resources/news/sitrof-introduces-fixed-price-migration/#comments</comments>
		<pubDate>Wed, 04 May 2011 16:28:37 +0000</pubDate>
		<dc:creator>Sitrof</dc:creator>
				<category><![CDATA[News]]></category>

		<guid isPermaLink="false">http://sitrof.com/?p=2907</guid>
		<description><![CDATA[Sitrof Technologies, the authority on unstructured document management, today announced their latest offering, Fixed-Price Migration.  A fresh approach to migration, Sitrof’s Fixed-Price Migration enables businesses to migrate content quickly, easily and cost-effectively from one repository to another—no matter what system the business is currently running (Documentum, FirstDoc, SharePoint, FileNET, DocuShare, etc.) Sitrof migrates a company’s [...]]]></description>
			<content:encoded><![CDATA[<p>Sitrof Technologies, the authority on unstructured document management, today announced their latest offering, Fixed-Price Migration.  A fresh approach to migration, Sitrof’s Fixed-Price Migration enables businesses to migrate content quickly, easily and cost-effectively from one repository to another—no matter what system the business is currently running (Documentum, FirstDoc, SharePoint, FileNET, DocuShare, etc.)</p>
<p>Sitrof migrates a company’s data, content and metadata--no matter how many repositories they have or need. And Sitrof guarantees that all migrations are performed successfully through strict validation requirements.</p>
<p>"Migrations are become a necessity based on the number of mergers and acquisitions taking place," said Bryan Reynolds, Managing Partner of Sitrof Technologies. "The fixed-price aspect means there are no surprises and budgets stay on track. Additionally, we are partnered with a variety of migration specialists and developed our own custom tools to make it the most efficient migration possible."</p>
<p>Practical expertise means Sitrof takes the risk out of system consolidation. For over a decade, Sitrof has performed complex migrations for Fortune 100 companies, successfully migrating content from a variety of sources to different target repositories in the Life Sciences and other highly regulated industries.</p>
<p>Fixed-Price Migration consolidates data, making the business more efficient. Additionally, Fixed-Price Migration is tailored to the client: a Sitrof Migration Analyst works through the Migration Checklist and delivers a plan. From there, it can be done on-site or off-site based on the business’ needs and cost requirements. For regulated and non-regulated environments alike, Sitrof is the trusted provider for complex content migrations.</p>
<p>For more information on Sitrof Fixed-Price Migration, <a href="http://sitrof.com/products/fixed-price-migration-from-sitrof/">click here</a>.</p>
<p><strong> </strong></p>
<p><strong>About Sitrof Technologies</strong><br />
Sitrof provides premier consulting and technology solutions enabling organizations to improve efficiencies and mitigate risk. Backed by decades of industry knowledge and world-class industry partnerships, Sitrof has saved millions of dollars and countless months of time, for hundreds of companies. For more information about Sitrof please visit <a href="../../../../../">http://sitrof.com</a></p>
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		<title>InfoWorld Green 15 Awards</title>
		<link>http://sitrof.com/resources/insights/sitrof-client-selected-for-infoworld-green-15-awards/</link>
		<comments>http://sitrof.com/resources/insights/sitrof-client-selected-for-infoworld-green-15-awards/#comments</comments>
		<pubDate>Wed, 27 Apr 2011 18:25:02 +0000</pubDate>
		<dc:creator>Sitrof</dc:creator>
				<category><![CDATA[Awards and Speaking]]></category>
		<category><![CDATA[Insights]]></category>
		<category><![CDATA[Document Management]]></category>
		<category><![CDATA[linkedin]]></category>
		<category><![CDATA[paperless office]]></category>

		<guid isPermaLink="false">http://sitrof.com/?p=2878</guid>
		<description><![CDATA[Sitrof client Copernicus Group IRB (CGIRB) recently won a prestigious IDG InfoWorld Green 15 Award. Copernicus Group IRB is a paperless office whose shift from being paper-based was led by Sitrof Technologies in a large, three-phase project. This has saved the organization more than $2 million on shipping, printing, postage, and file storage. Sitrof’s installation has [...]]]></description>
			<content:encoded><![CDATA[<p><strong>Sitrof client Copernicus Group IRB (CGIRB) recently won a prestigious IDG InfoWorld Green 15 Award.</strong></p>
<p>Copernicus Group IRB is a paperless office whose shift from being  paper-based was led by Sitrof Technologies in a large, three-phase project. This has saved the organization more than $2 million  on shipping, printing, postage, and file storage. Sitrof’s installation  has translated to CGIRB becoming 98% paperless.</p>
<p>CGIRB was honored by InfoWorld for being one of the most innovative IT initiatives that fall under the<span style="text-decoration: underline;"> </span>umbrella of sustainability. The award honors companies who have embraced green technology to drive projects and develop products aimed at boosting energy efficiency, trimming waste, and reducing or eliminating the use or the production of harmful substances are selected for the Green 15.</p>
<p>CGIRB staff can now digitally search through 5 million pages' worth of legacy documents and process client submissions into the electronic workflow in an average of 3.7 minutes, as compared to 104 minutes in its paper-based era. Less time, money and effort are spent on everyday tasks, making CGIRB more efficient and green, thanks to the Sitrof installation.</p>
<p>To learn more about the InfoWorld Green 15 and read the complete list of winners, please <a href="http://www.infoworld.com/d/data-center/the-green-it-stars-2011-549?page=0,0" target="_blank">click here</a>.<br />
To read the full case study on Sitrof and CGIRB, please <a href="http://sitrof.com/resources/copernicus-group-irb-case-study/" target="_blank">click here</a>.</p>
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