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URL: https://www.medialab.com/iqe-for-laboratories
Submission: On August 24 via api from US — Scanned from US

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      <div class="text">MediaLab's Intelligent Quality Engine (IQE) solution is designed to deliver powerful automation for laboratory non-conforming event management processes. IQE eliminates the need for paper-based, manual investigation and CAPA
        processes, while reducing cost and supporting the quality improvement program. IQE helps your laboratory follow corrective and preventive action standards as outlined by CAP, Joint Commission, ISO, and other accrediting bodies. You'll benefit
        from a streamlined approach that supports your regulatory compliance.</div>
      <div class="row">
        <div class="col-12 col-lg-auto mb-2">
          <div class="buttonpadding"><button type="button" class="btn btn-primary rounded mlbutton" data-toggle="modal" data-target="#mlModal" onclick="SetModalContent('Request Demo or Trial','/omniform.aspx');">Request Demo or Trial</button></div>
        </div>
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            onclick="SetModalContent('Ask a Question','/shortform.aspx?messagetext=I+would+like+more+information+about+IQE+for+Laboratories.');">Ask a Question</button></div>
        <div class="col-12 col-lg-auto mb-2"><a href="/quote.aspx" class="btn btn-primary rounded mlbutton">Get a Quote</a></div>
      </div>
      <div class="homepagespacer"></div>
      <div class="container">
        <div class="row">
          <div class="col-12 col-md-9">
            <h2>Manage NCEs / CAPAs Through Their Whole Lifecycle</h2>
            <div class="text">Start by using our online form templates, or create your own. Allow employees to create events as problems arise. MediaLab will route your event through each phase of the event management lifecycle, from initial event
              description to risk analysis, closure, and change effectiveness evaluations.</div>
            <div class="popopenlink lvar6" id="link_e04b87cc-02e0-442c-affe-e8d105f6e6c4">
              <a class="nocolor" href="#" onclick="Popopen('e04b87cc-02e0-442c-affe-e8d105f6e6c4'); return false;">Learn about the NCE / CAPA lifecycle <i class="fal fa-caret-right" id="arrow_e04b87cc-02e0-442c-affe-e8d105f6e6c4"></i></a></div>
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              <div class="text">All CAPA events follow a lifecycle, from description and risk assessment, to investigation, corrective &amp; preventive action, and evaluation of effectiveness. Each phase asks appropriate, customizable questions to
                collect necessary information.</div>
              <div class="text">Use the Five-Whys tool to help get at the root cause of the problem. List causes of the event and ask “why?” as many times as needed to dig down to the source of the issue, and then generate remediation actions to
                address the root cause.</div>
              <div class="text">IQE's collaboration tools make it easy to get feedback from other parties who were involved in an event or whose feedback is needed. Request collaboration from any user in MediaLab or outside users as well. Collaborate
                on completing the form by letting these users fill in appropriate fields, while preventing them from changing sections that they shouldn't.</div>
              <div class="text">Event owners are responsible for guiding non-conforming events through the CAPA lifecycle of description, risk assessment, investigation, corrective &amp; preventive action, and evaluation of effectiveness. They can
                request collaboration and feedback from other users, allowing everyone to contribute to continuous quality improvement.</div>
              <div class="text">Get 21 CFR Part 11 compliant electronic signatures on your event. You can request signatures at any point in the CAPA lifecycle and from any user.</div>
            </div>
            <div class="popopenspacer"></div>
          </div>
          <div class="col-12 col-md-3">
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        </div>
      </div>
      <div class="homepagespacer"></div>
      <div class="container">
        <div class="row">
          <div class="col-12 col-md-9">
            <h2>Your Forms, Made Better</h2>
            <div class="text">Your current processes and forms work beautifully in IQE. We'll show you how to create your own custom forms (non-conforming event, change control, failed PT investigations, and more) using our flexible form builder.
              Customize workflows, collaborations, approval requests, and reports. Take spreadsheets out of the picture and start enjoying the power of automation.</div>
            <div class="popopenlink lvar6" id="link_8495db50-8b83-482d-8f51-7f1b1c2bf37e">
              <a class="nocolor" href="#" onclick="Popopen('8495db50-8b83-482d-8f51-7f1b1c2bf37e'); return false;">How can IQE improve quality management? <i class="fal fa-caret-right" id="arrow_8495db50-8b83-482d-8f51-7f1b1c2bf37e"></i></a></div>
            <div class="popopen var6" id="8495db50-8b83-482d-8f51-7f1b1c2bf37e" style="display: none;">
              <div class="text">No need for paper-based event forms, manual collaboration processes, or spreadsheets managing your nonconforming event data. Increase your CAPA productivity using our centralized online system. Upload supporting
                documentation directly into IQE. Collect feedback from employees and administrators right from your forms. Assign and collect 21 CFR Part 11 compliant approval and evaluation electronic signatures.</div>
              <div class="text">One central, organized to-do list provides a hub for all the activities that your users need to complete in IQE. No hunting for the right event or getting lost in the shuffle.</div>
              <div class="text">Reminders and notifications are sent to your users automatically, so they stay on top of what they need to do to properly close out events. Customize how frequently your users get notifications and reminders from IQE.
              </div>
              <div class="text">IQE keeps track of every event view and every change. You have a full audit trail of all user activity to see exactly how your users are interacting with your events.</div>
              <div class="text">IQE comes with several out-of-the-box reports for our template forms, but you have full control to customize and save your reports to see exactly the data you need. Automatically include summary tables, charts, and
                graphs of your data. Filter and drill-down into data by multiple dimensions to isolate trends and problems.</div>
              <div class="text">See how your forms change over time. As modifications are needed, MediaLab automatically keeps track of previous versions of the form, so you can see the form just as it was when your users filled out events. Users
                work from forms that have been approved by your lab director, quality managers, or other key personnel.</div>
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      </div>
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      <div class="container">
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            <h2>Intelligent Access Control</h2>
            <div class="text">You can assign roles to individual users or to groups of users based on title, job description, or laboratory function. Users can see only what's need for their role. Get collaboration from other users without revealing
              all details of the event or follow-up.</div>
            <div class="popopenlink lvar6" id="link_bad540f4-dd24-4567-af68-388aa1c4dcd5">
              <a class="nocolor" href="#" onclick="Popopen('bad540f4-dd24-4567-af68-388aa1c4dcd5'); return false;">Learn more about access control <i class="fal fa-caret-right" id="arrow_bad540f4-dd24-4567-af68-388aa1c4dcd5"></i></a></div>
            <div class="popopen var6" id="bad540f4-dd24-4567-af68-388aa1c4dcd5" style="display: none;">
              <div class="text">Select users who can create and edit forms, who can start events for which forms, and who can own events for which forms. Limit administrative access to just a handful of users, or let each department supervisor manage
                their own non-conforming events.</div>
              <div class="text">Let all your users have some access to IQE. They can start reporting on events that they encounter and provide the initial description. Events are then handed off to event owners, who complete the CAPA lifecycle for
                each event.</div>
              <div class="text">All events have an owner that's responsible for making sure the CAPA lifecycle gets complete. Owners are reminded whenever an event stalls that their attention is needed to remedy the situation.</div>
              <div class="text">All your laboratory employees can take advantage of IQE's online forms to start recording events and provide initial description. These events are then handed off to owners (quality personnel, supervisors) for further
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      </div>
      <div class="homepagespacer"></div>
      <div class="container">
        <div class="row">
          <div class="col-12 col-md-9">
            <h2>Powerful Reporting for Tracking and Trending</h2>
            <div class="text">
              <div class="text">Tracking and trending has never been easier. IQE's robust reporting and data engine allows you to control your event statuses, tracking/trending reports, dashboards, event retrieval, and more. Use standard reports or
                filter by user-defined criteria. View all events by type, location, date, and more. Your data is viewable in real-time, all the time. Export your data into PDF, PowerPoint and Excel reports for quality committee presentations.</div>
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            <div class="popopenlink lvar6" id="link_32abf4ba-eea8-4318-82df-7f9350ed5525">
              <a class="nocolor" href="#" onclick="Popopen('32abf4ba-eea8-4318-82df-7f9350ed5525'); return false;">Learn more about dashboards and reporting <i class="fal fa-caret-right" id="arrow_32abf4ba-eea8-4318-82df-7f9350ed5525"></i></a></div>
            <div class="popopen var6" id="32abf4ba-eea8-4318-82df-7f9350ed5525" style="display: none;">
              <div class="text">IQE's intelligent dashboards and reporting helps you locate errors quickly and work to a resolution that prevents reoccurrences. Dashboards highlight how your non-conforming events are moving through the CAPA lifecycle
                of description, investigation, corrective &amp; preventive action, and reporting.</div>
              <div class="text">IQE can generate PDF copies of your forms and events for archival purposes, as well as PDF copies of your reports that can be downloaded to your computer or saved within IQE for future review. IQE also exports Excel
                spreadsheets of your reports, so you can do additional reporting and searching in Excel.</div>
            </div>
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            <div class="padleftright"><img
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      </div>
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            <h2>A Key Part of Risk Management</h2>
            <div class="text">Repeated non-conforming events and their subsequent investigation and mitigation cause avoidable risks and takes up time, especially without an automated system in place. IQE will help your laboratory monitor your
              important metrics with our real-time reports and dashboards. Follow-up tasks are scheduled, employees are notified, and processes are made efficient.</div>
          </div>
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            <div class="padleftright"><img
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      </div>
      <div class="homepagespacer"></div>
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            <h2>Integrated Across the MediaLab Quality Management Platform</h2>
            <div class="text">Integrated into MediaLab's platform of quality software, IQE connects with our Document Control, InspectionProof, and Compliance &amp; CE systems. Easily annotate changes to SOPs and policies and provide training updates
              to lab team members to fulfill change control requirements.</div>
          </div>
          <div class="col-12 col-md-3">
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          <div class="buttonpadding"><button type="button" class="btn btn-primary rounded mlbutton" data-toggle="modal" data-target="#mlModal" onclick="SetModalContent('Request Demo or Trial','/omniform.aspx');">Request Demo or Trial</button></div>
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   maintenance, quality metrics) Exam Simulators Case Simulators
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IQE FOR LABORATORIES

MediaLab's Intelligent Quality Engine (IQE) solution is designed to deliver
powerful automation for laboratory non-conforming event management processes.
IQE eliminates the need for paper-based, manual investigation and CAPA
processes, while reducing cost and supporting the quality improvement program.
IQE helps your laboratory follow corrective and preventive action standards as
outlined by CAP, Joint Commission, ISO, and other accrediting bodies. You'll
benefit from a streamlined approach that supports your regulatory compliance.
Request Demo or Trial
Ask a Question
Get a Quote



MANAGE NCES / CAPAS THROUGH THEIR WHOLE LIFECYCLE

Start by using our online form templates, or create your own. Allow employees to
create events as problems arise. MediaLab will route your event through each
phase of the event management lifecycle, from initial event description to risk
analysis, closure, and change effectiveness evaluations.
Learn about the NCE / CAPA lifecycle
All CAPA events follow a lifecycle, from description and risk assessment, to
investigation, corrective & preventive action, and evaluation of effectiveness.
Each phase asks appropriate, customizable questions to collect necessary
information.
Use the Five-Whys tool to help get at the root cause of the problem. List causes
of the event and ask “why?” as many times as needed to dig down to the source of
the issue, and then generate remediation actions to address the root cause.
IQE's collaboration tools make it easy to get feedback from other parties who
were involved in an event or whose feedback is needed. Request collaboration
from any user in MediaLab or outside users as well. Collaborate on completing
the form by letting these users fill in appropriate fields, while preventing
them from changing sections that they shouldn't.
Event owners are responsible for guiding non-conforming events through the CAPA
lifecycle of description, risk assessment, investigation, corrective &
preventive action, and evaluation of effectiveness. They can request
collaboration and feedback from other users, allowing everyone to contribute to
continuous quality improvement.
Get 21 CFR Part 11 compliant electronic signatures on your event. You can
request signatures at any point in the CAPA lifecycle and from any user.





YOUR FORMS, MADE BETTER

Your current processes and forms work beautifully in IQE. We'll show you how to
create your own custom forms (non-conforming event, change control, failed PT
investigations, and more) using our flexible form builder. Customize workflows,
collaborations, approval requests, and reports. Take spreadsheets out of the
picture and start enjoying the power of automation.
How can IQE improve quality management?
No need for paper-based event forms, manual collaboration processes, or
spreadsheets managing your nonconforming event data. Increase your CAPA
productivity using our centralized online system. Upload supporting
documentation directly into IQE. Collect feedback from employees and
administrators right from your forms. Assign and collect 21 CFR Part 11
compliant approval and evaluation electronic signatures.
One central, organized to-do list provides a hub for all the activities that
your users need to complete in IQE. No hunting for the right event or getting
lost in the shuffle.
Reminders and notifications are sent to your users automatically, so they stay
on top of what they need to do to properly close out events. Customize how
frequently your users get notifications and reminders from IQE.
IQE keeps track of every event view and every change. You have a full audit
trail of all user activity to see exactly how your users are interacting with
your events.
IQE comes with several out-of-the-box reports for our template forms, but you
have full control to customize and save your reports to see exactly the data you
need. Automatically include summary tables, charts, and graphs of your data.
Filter and drill-down into data by multiple dimensions to isolate trends and
problems.
See how your forms change over time. As modifications are needed, MediaLab
automatically keeps track of previous versions of the form, so you can see the
form just as it was when your users filled out events. Users work from forms
that have been approved by your lab director, quality managers, or other key
personnel.





INTELLIGENT ACCESS CONTROL

You can assign roles to individual users or to groups of users based on title,
job description, or laboratory function. Users can see only what's need for
their role. Get collaboration from other users without revealing all details of
the event or follow-up.
Learn more about access control
Select users who can create and edit forms, who can start events for which
forms, and who can own events for which forms. Limit administrative access to
just a handful of users, or let each department supervisor manage their own
non-conforming events.
Let all your users have some access to IQE. They can start reporting on events
that they encounter and provide the initial description. Events are then handed
off to event owners, who complete the CAPA lifecycle for each event.
All events have an owner that's responsible for making sure the CAPA lifecycle
gets complete. Owners are reminded whenever an event stalls that their attention
is needed to remedy the situation.
All your laboratory employees can take advantage of IQE's online forms to start
recording events and provide initial description. These events are then handed
off to owners (quality personnel, supervisors) for further progress through the
CAPA lifecycle. Details are then hidden from your regular users, unless they
have specific permissions to view events.





POWERFUL REPORTING FOR TRACKING AND TRENDING

Tracking and trending has never been easier. IQE's robust reporting and data
engine allows you to control your event statuses, tracking/trending reports,
dashboards, event retrieval, and more. Use standard reports or filter by
user-defined criteria. View all events by type, location, date, and more. Your
data is viewable in real-time, all the time. Export your data into PDF,
PowerPoint and Excel reports for quality committee presentations.
Learn more about dashboards and reporting
IQE's intelligent dashboards and reporting helps you locate errors quickly and
work to a resolution that prevents reoccurrences. Dashboards highlight how your
non-conforming events are moving through the CAPA lifecycle of description,
investigation, corrective & preventive action, and reporting.
IQE can generate PDF copies of your forms and events for archival purposes, as
well as PDF copies of your reports that can be downloaded to your computer or
saved within IQE for future review. IQE also exports Excel spreadsheets of your
reports, so you can do additional reporting and searching in Excel.





A KEY PART OF RISK MANAGEMENT

Repeated non-conforming events and their subsequent investigation and mitigation
cause avoidable risks and takes up time, especially without an automated system
in place. IQE will help your laboratory monitor your important metrics with our
real-time reports and dashboards. Follow-up tasks are scheduled, employees are
notified, and processes are made efficient.




INTEGRATED ACROSS THE MEDIALAB QUALITY MANAGEMENT PLATFORM

Integrated into MediaLab's platform of quality software, IQE connects with our
Document Control, InspectionProof, and Compliance & CE systems. Easily annotate
changes to SOPs and policies and provide training updates to lab team members to
fulfill change control requirements.


Request Demo or Trial
Ask a Question
Get a Quote
 



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