Intagras provides software and services to assist with managing your pharmaceutical product labeling process based on global and local requirements and your standard operating procedures. Be proactive with pharma compliance with the support of Intagras’
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Regulatory Compliance Software | Intagras | intagras.com Reviews
https://intagras.com
Intagras provides software and services to assist with managing your pharmaceutical product labeling process based on global and local requirements and your standard operating procedures. Be proactive with pharma compliance with the support of Intagras’
Blog Intagras | Just another WordPress site
DIA Pharmacovigilance and Risk Management Strategies Meeting. FDA Requires Unique Device Identification Intagras Blog. SPL grapic on FDA utilization. DIA Pharmacovigilance and Risk Management Strategies Meeting. I attended the DIA Pharmacovigilance and Risk Management Strategies meeting this week in Washington, DC. The meeting’s focus was a combination of risk management planning, drug safety, novel data mining methods for signals and evidence including social media and emerging markets. Rob Leonetti, VP.
intagras.com
Pharmaceutical Labeling Technology | Intagras
http://www.intagras.com/our-products.aspx
SPL Portal Data Sheet. To that end, when we set out to develop the leading-edge applications our clients use daily, we. Begin by making informed assumptions. Ensure our architecture is built for change. Discover more about our best-in-class labeling technology applications and how they can help your company achieve and maintain compliance with your regulatory agencies. Website development by Bayshore Solutions.
Pharma Labeling Software Support| Intagras
http://www.intagras.com/support.aspx
To this end, our Intagras software support representatives undergo rigorous training aimed at ensuring a clear and comprehensive understanding of our customers’ industries, as well as a familiarity with the common issues they experience. From there, they are trained in a systematic approach to problem definition and resolution that emphasizes permanent fixes, not band-aid solutions. The goal is to keep you moving forward, no matter what may occur. Website development by Bayshore Solutions.
Product Submissions & FDA Submissions | Intagras
http://www.intagras.com/our-services.aspx
Our services and our people. Managing product labeling within the pharmaceutical industry is a complex task made even more difficult by the necessity of maintaining compliance with health authority requirements, depending on the global reach of your organization. Since 2005, pharmaceutical regulatory agencies have continued to expand electronic submission requirements. Current draft guidance continues to show that pharmaceutical regulatory agencies will only continue to expand and leverage the ca...
Customer Service
http://www.intagras.com/support/customer-service.aspx
Intagras believes that excellent customer service is the essential follow-on from excellent products. We are never satisfied until we know that you are satisfied. That is the basis of everything we undertake on your behalf. Customer Service can be reached at the following numbers:. You may also reach Customer Service via email by filling out the form below:. Website development by Bayshore Solutions.
Sales Department
http://www.intagras.com/support/sales-department.aspx
We want to hear from you. We appreciate your interest in our products and services. We believe that our applications are best in class and can benefit your organization in a number of ways. Our focus is always on ensuring that your workflow is streamlined, as well as bringing increased efficiencies and effectiveness to your SPL efforts. Let us show you how by scheduling a live demonstration of any of our products. Sales can be reached at the following numbers:. GDT Portal (Global Decision Tracking).
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Interesting Article | Blog Intagras
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DIA Pharmacovigilance and Risk Management Strategies Meeting. FDA Requires Unique Device Identification Intagras Blog. SPL grapic on FDA utilization. It is exciting to see that the FDA is continuing to expand electronic labeling! Full report (25 pages). Http:/ www.gao.gov/assets/660/655760.pdf. Http:/ www.gao.gov/assets/660/655761.pdf. This entry was posted in Electronic Labeling. July 10, 2013. SPL grapic on FDA utilization →. Leave a Reply Cancel reply. You must be logged in. To post a comment.
SPL grapic on FDA utilization | Blog Intagras
http://blog.intagras.com/spl-grapic-on-fda-utilization
DIA Pharmacovigilance and Risk Management Strategies Meeting. FDA Requires Unique Device Identification Intagras Blog. SPL grapic on FDA utilization. SPL grapic on FDA utilization. Here is an e-mail that was sent out by Lonnie Smith of the FDA. The e-mail provides a link that has a graphic of how three different Federal government agencies may utilize a single product SPL file for different purposes. Begin E-mail from FDA * * *. This entry was posted in Electronic Labeling. August 26, 2013.
admin | Blog Intagras
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DIA Pharmacovigilance and Risk Management Strategies Meeting. FDA Requires Unique Device Identification Intagras Blog. SPL grapic on FDA utilization. DIA Pharmacovigilance and Risk Management Strategies Meeting. I attended the DIA Pharmacovigilance and Risk Management Strategies meeting this week in Washington, DC. The meeting’s focus was a combination of risk management planning, drug safety, novel data mining methods for signals and evidence including social media and emerging markets. Rob Leonetti, VP.
Global Unique Device Identification Database | Blog Intagras
http://blog.intagras.com/tag/global-unique-device-identification-database
Tag Archives: Global Unique Device Identification Database. FDA Requires Unique Device Identification Intagras Blog. On Tuesday, September 24th 2013, the Department of Health and Human Services (HHS) published the following in the Federal Register Volume 78, Number 185, Part V, requiring a Medical Device Unique Device Identification System. Link to the Federal Register Volume 78, Number 185, Part V: http:/ www.gpo.gov/fdsys/pkg/FR-2013-09-24/pdf/2013-23059.pdf. This entry was posted in UDI.
Global Labeling Tracking | Blog Intagras
http://blog.intagras.com/category/global-labeling-tracking
DIA Pharmacovigilance and Risk Management Strategies Meeting. FDA Requires Unique Device Identification Intagras Blog. SPL grapic on FDA utilization. Category Archives: Global Labeling Tracking. DIA Pharmacovigilance and Risk Management Strategies Meeting. Http:/ www.diahome.org/Tools/Content.aspx? Is your organization as prepared for efficient labeling updates as it could be? Http:/ www.intagras.com. Rob Leonetti, VP. This entry was posted in Global Labeling Tracking. January 20, 2014.
UDI | Blog Intagras
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FDA Requires Unique Device Identification Intagras Blog. On Tuesday, September 24th 2013, the Department of Health and Human Services (HHS) published the following in the Federal Register Volume 78, Number 185, Part V, requiring a Medical Device Unique Device Identification System. Link to the Federal Register Volume 78, Number 185, Part V: http:/ www.gpo.gov/fdsys/pkg/FR-2013-09-24/pdf/2013-23059.pdf. For more additional information, please feel free to contact me at info@intagras.com. September 26, 2013.
GUDID | Blog Intagras
http://blog.intagras.com/tag/gudid
FDA Requires Unique Device Identification Intagras Blog. On Tuesday, September 24th 2013, the Department of Health and Human Services (HHS) published the following in the Federal Register Volume 78, Number 185, Part V, requiring a Medical Device Unique Device Identification System. Link to the Federal Register Volume 78, Number 185, Part V: http:/ www.gpo.gov/fdsys/pkg/FR-2013-09-24/pdf/2013-23059.pdf. For more additional information, please feel free to contact me at info@intagras.com. September 26, 2013.
FDA Requires Unique Device Identification | Intagras Blog | Blog Intagras
http://blog.intagras.com/spl-for-medical-device-unique-device-identification
DIA Pharmacovigilance and Risk Management Strategies Meeting. FDA Requires Unique Device Identification Intagras Blog. SPL grapic on FDA utilization. FDA Requires Unique Device Identification Intagras Blog. On Tuesday, September 24th 2013, the Department of Health and Human Services (HHS) published the following in the Federal Register Volume 78, Number 185, Part V, requiring a Medical Device Unique Device Identification System. This entry was posted in UDI. September 26, 2013. Leave a Reply Cancel reply.
Unique Device Identifier | Blog Intagras
http://blog.intagras.com/tag/unique-device-identifier
Tag Archives: Unique Device Identifier. FDA Requires Unique Device Identification Intagras Blog. On Tuesday, September 24th 2013, the Department of Health and Human Services (HHS) published the following in the Federal Register Volume 78, Number 185, Part V, requiring a Medical Device Unique Device Identification System. Link to the Federal Register Volume 78, Number 185, Part V: http:/ www.gpo.gov/fdsys/pkg/FR-2013-09-24/pdf/2013-23059.pdf. This entry was posted in UDI. September 26, 2013.
DIA Pharmacovigilance and Risk Management Strategies Meeting | Blog Intagras
http://blog.intagras.com/dia-pharmacovigilance-and-risk-management-strategies-meeting
DIA Pharmacovigilance and Risk Management Strategies Meeting. FDA Requires Unique Device Identification Intagras Blog. SPL grapic on FDA utilization. DIA Pharmacovigilance and Risk Management Strategies Meeting. I attended the DIA Pharmacovigilance and Risk Management Strategies meeting this week in Washington, DC. The meeting’s focus was a combination of risk management planning, drug safety, novel data mining methods for signals and evidence including social media and emerging markets. Rob Leonetti, VP.
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Regulatory Compliance Software | Intagras
Intagras specializes in making the regulatory process manageable as well as intuitive for life sciences, pharmaceutical and other companies marketing medicines and more. Tracing all the updates for all affiliates is both time consuming and costly, and frequently complicated by inaccurate methods of updating and tracking. Discover more about the robust suite of powerful, fully configurable structured authoring solutions offered by Intagras. Pharmaceutical and Medical Device compliance functionality for FD...
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