Perficient’s life sciences practice once had a manual, time-consuming and expensive process for signing and collecting validation documents. From handwritten signatures to scanning and shipping documents all over the globe, it was only a matter of time before we made the move to 21 CFR Part 11-compliant digital signatures.
Michelle Engler, an expert in the development of clinical applications, discussed our experience implementing a digital signature solution and how your organization can benefit from one too.
During the presentation, we will covered:
-Cost-benefit analysis
-Solution selection and implementation
-21 CFR Part 11 system validation
-Lessons learned
Data integrity - Regulatory Perspective and Challenges: santoshnarla
Data Integrity: Regulatory Perspective and Challenges.
This presentation will present the importance of data integrity in the pharma industry with regards to the quality compliance and its impact on industry. This presentation also emphasizes on importance of regulatory affairs department in ensuring the data integrity and regulatory challenges.
Webinar: Europe's new Medical Device Regulations (MDR)EMERGO
WATCH the recorded webinar here: http://www.emergogroup.com/resources/video-webinar-europe-mdr-changes
The first major revision to device regulations since 2007 has been released and the changes are significant. Although the MDR won't take effect until early 2020, smart companies are planning ahead to beat the crush of companies that will inevitably wait until the last minute, overwhelming EU Notified Bodies. Ronald Boumans, Senior Global Regulatory Consultant for EMERGO (and former IGZ compliance inspector in The Netherlands) outlines the most important changes you need to know in this 35 minute recorded webinar from September 2016. Topics addressed include:
How the MDR is organized
Scope of the legislation
Device classification rules
New clinical evaluation requirements
UDI and EUDAMED database
Adverse event reporting
And much more...
Migrating from Oracle AERS to Argus Safety: Reasons for the MovePerficient, Inc.
Not too long ago, Oracle AERS was the most widely-used adverse event report system. However, with the acquisition of Relsys and its safety and pharmacovigilance system in 2009, Argus Safety quickly became the go-to software for most life sciences companies. Its capabilities and comprehensiveness are unmatched.
Companies currently using Oracle AERS have expressed interest in moving to Argus Safety, but want to know more before making the jump. This webinar is meant to do just that – answer your common questions.
Please join Perficient's Dr. Rodney Lemery, director of safety and pharmacovigilance, as he will:
Compare Argus Safety to AERS
Cover the options of effectively migrating to Argus Safety
Efficient Trial Management through Unified CTMS and Study Start-upVeeva Systems
Learn the benefits of a unified clinical landscape, particularly how clinical trial management software (CTMS) and study start-up applications lead to more efficient trial management when working in concert with one another.
Speed Clinical Trials from Start to Close: The Path to a Modern CTMSVeeva Systems
Learn how a modern CTMS leads to better oversight, study analytics, and risk identification. This presentation also covers common barriers to the migration process and how to overcome them. Watch a demonstration of Veeva Vault CTMS: http://bit.ly/VaultCTMSDemo
Data integrity - Regulatory Perspective and Challenges: santoshnarla
Data Integrity: Regulatory Perspective and Challenges.
This presentation will present the importance of data integrity in the pharma industry with regards to the quality compliance and its impact on industry. This presentation also emphasizes on importance of regulatory affairs department in ensuring the data integrity and regulatory challenges.
Webinar: Europe's new Medical Device Regulations (MDR)EMERGO
WATCH the recorded webinar here: http://www.emergogroup.com/resources/video-webinar-europe-mdr-changes
The first major revision to device regulations since 2007 has been released and the changes are significant. Although the MDR won't take effect until early 2020, smart companies are planning ahead to beat the crush of companies that will inevitably wait until the last minute, overwhelming EU Notified Bodies. Ronald Boumans, Senior Global Regulatory Consultant for EMERGO (and former IGZ compliance inspector in The Netherlands) outlines the most important changes you need to know in this 35 minute recorded webinar from September 2016. Topics addressed include:
How the MDR is organized
Scope of the legislation
Device classification rules
New clinical evaluation requirements
UDI and EUDAMED database
Adverse event reporting
And much more...
Migrating from Oracle AERS to Argus Safety: Reasons for the MovePerficient, Inc.
Not too long ago, Oracle AERS was the most widely-used adverse event report system. However, with the acquisition of Relsys and its safety and pharmacovigilance system in 2009, Argus Safety quickly became the go-to software for most life sciences companies. Its capabilities and comprehensiveness are unmatched.
Companies currently using Oracle AERS have expressed interest in moving to Argus Safety, but want to know more before making the jump. This webinar is meant to do just that – answer your common questions.
Please join Perficient's Dr. Rodney Lemery, director of safety and pharmacovigilance, as he will:
Compare Argus Safety to AERS
Cover the options of effectively migrating to Argus Safety
Efficient Trial Management through Unified CTMS and Study Start-upVeeva Systems
Learn the benefits of a unified clinical landscape, particularly how clinical trial management software (CTMS) and study start-up applications lead to more efficient trial management when working in concert with one another.
Speed Clinical Trials from Start to Close: The Path to a Modern CTMSVeeva Systems
Learn how a modern CTMS leads to better oversight, study analytics, and risk identification. This presentation also covers common barriers to the migration process and how to overcome them. Watch a demonstration of Veeva Vault CTMS: http://bit.ly/VaultCTMSDemo
Executing Validation of GxP Systems Electronically using SharePointMontrium
Executing Validation of GxP
Systems Electronically using
SharePoint
For more information on Montrium please visit:
- www.montrium.com
- www.twitter.com/Montrium
- www.youtube.com/Montrium
or email info@montrium.com
Importance of data standards and system validation of software for clinical r...Wolfgang Kuchinke
We present our evaluation of existing data standards for clinical trials. For this purpose a survey about the importance of data standards for clinical trials centers and EDC software companies were conducted. Electronic data capture in clinical trials uses a computerized system designed for the collection of clinical data in electronic form in Case Report Forms (CRF). It also covers medical data captured during clinical trials, safety data related to clinical trials, and patient reported outcome. The degree of implementation of standards, like CDISC ODM in available EDC software products was evaluated. Failure to establish data standards will make it difficult or impossible to connect data between different systems for efficient clinical study execution. The next step after purchasing a software solution is the computer system validation. Validation is about bringing computerized systems into regulatory compliance and making them compliant with GCP, GLP and GMP and other regulations (e.g. data protection). The basis standard for validation is provided by the GAMP Good Practice Guide, which provides a framework of best practices to ensure that computer systems are suitable for use and compliant with the legislation. The newest version uses a risk-based approach to computer system validation A system is evaluated and assigned to a predefined category based on its intended use and complexity. For validation one should define how all elements of the computer system are supposed to work (functional requirements), develop corresponding scripts and test routines to validate it is functioning as it should.
An audit trail in clinical research refers to a documented record of all activities and events related to the planning, conduct, and reporting of a clinical trial or research study. It provides a chronological and detailed account of actions taken, decisions made, and changes implemented throughout the course of the study. The primary purpose of maintaining an audit trail is to ensure the integrity, traceability, and transparency of clinical research data and processes. Here's a more in-depth look at the concept of an audit trail in clinical research:
Prioritizing Documentation for MDR Transition PlanningGreenlight Guru
This session will discuss the one year delay of the MDR date of application as well as some strategies to employ during the MDR Transition. In addition, some approaches for determining documents to prioritize for the transition will be discussed.
This session took place live at the Greenlight Guru True Quality Virtual Summit, a three-day event for medical device professionals to learn to get their devices to market faster, stay ahead of regulatory changes, and use quality as their multiplier to grow their device business.
Your next RIM solution - 3 key considerations for your moveV E R A
Considering to move to a new Regulatory Information Management system? Have a look at our pick of the 3 key considerations while moving to a new RIM system.
If you wish to receive more information - write us at info@cunesoft.com or visit our page https://cunesoft.com/en/products/rim/
Process Validation Master Planning DMAIC FusionGENEO
Process validation is a risk management verification activity for medical device and pharma companies. DMAIC is a well established methodology for improving process reliability, improving businesses and solving problems. This presentation discussed a logical fusion of these approaches. It includes a description of the validation life cycle. The business case for good validation is illustrated graphically. Contact us at ARVExcellence.com if you would like a copy.
ARV Excellence is a training and consulting firm based in Galway, Ireland with specialities in medical devices, and drug device combination product processes and process related problem solving
QMSR Harmonization: The Future of FDA's Quality Management System RegulationGreenlight Guru
Learn about the future of FDA's Quality Management System regulation.
This presentation originally aired during the 2022 Future of QMS Requirements Virtual Summit.
Improving Clinical Trial Performance: Part 3 - Streamline Trial Management wi...Veeva Systems
Henry Galio shares findings from the Unified Clinical Operations Survey and how research organizations can streamline trial management with Veeva Vault CTMS. Access the webinar > http://go.veeva.com/ModernCTMS
Agile Computer System Validation of software productsWolfgang Kuchinke
Personalized medicine seems to be a potential solution to the known challenges facing clinical research and drug development. To be employed in clinical research, software tools must undergo a process called Computer System Validation (CSV) for compliance with legal requirements and Good Clinical Practice (GCP). Four academic developer groups of the EU project p-medicine were surveyed to evaluate the readiness of their developed software products to be used for clinical research. The analysis of the survey showed that considerable gaps exist in tool maintenance, quality management and compliance documentation. Because all developer groups use agile development methods, recommendations for agile quality assurance were developed as well as for using agile methods to establish “compliance by design”. We show how agile validation can be established by small modifications of sprint processes.
ISO/IEC 27701 vs. ISO/IEC 27001 vs. NIST: Essential Things You Need to KnowPECB
Just a few days ago NIST published a complete refresh of the SP800-53, which provides a catalog of security measure to protect an organization against a variety of risks and threats.
How might NIST guidance fit in an information security management system like ISO/IEC 27001 and its privacy extension ISO/IEC 27701?
In this session, we will make a quick walk-through the standards and best practices, compare them, and find out how they map and differ from one another.
The webinar will cover:
• A quick recap of the topics covered in ISO27001/ISO27701
• Discovering the NIST guidelines for Information & cyber Security (SP800-SP1800)
• Main differences and mappings between NIST guidance and ISO27001
• About the latest publication (sep/2020) on NIST SP800-53 (Security and Privacy Controls for Information Systems and Organizations)
• Implementing information & cyber-security best practices
Date: October 14, 2020
YouTube presentation: https://youtu.be/zfsxSaaErqg
-------------------------------------------------------------------------------
Find out more about ISO training and certification services
Training: https://pecb.com/whitepaper/iso-27001-information-technology--security-techniques-information-security--management-systems---requirements
https://pecb.com/en/education-and-certification-for-individuals/iso-iec-27701
Webinars: https://pecb.com/webinars
Article: https://pecb.com/article
Whitepaper: https://pecb.com/whitepaper
-------------------------------------------------------------------------------
For more information about PECB:
Website: https://pecb.com/
LinkedIn: https://www.linkedin.com/company/pecb/
Facebook: https://www.facebook.com/PECBInternational/
Slideshare: http://www.slideshare.net/PECBCERTIFICATION
Strategies for Conducting GxP Vendor Assessment of Cloud Service Providers - ...Montrium
Want to deploy a new technology solution but not sure where to begin? These slides cover key considerations for choosing a vendor with cloud compliance and validation in mind. With the Office 365 subscription-based service gaining considerable momentum in the life sciences, it's important to stay ahead of the technological and regulatory curve and consider how an EDMS system will bring improvements to managing your GxP content.
Here we cover the following topics:
-Vendor assessment of Microsoft
-Subscription basics of Office 365
-Review of ISO/SOC audit reports
-Ensuring that no critical observations are made
-Security and quality controls in place
You can follow along with this presentation via webinar format:
https://info.montrium.com/strategies-for-conducting-gxp-vendor-assessment-of-cloud-service-providers
eCOA and ePRO and Their Use in Clinical Trials_pptxClinosolIndia
Virtual clinical trials are becoming even more popular because of technology advances. They offer enormous benefits to sponsors and patients. However, there are challenges. One of the key elements of a virtual clinical trial is ePRO and eCOA.
Patient-reported outcome (PRO) endpoints are often necessary to adequately evaluate the treatment benefit provided by new medical products (e.g., drugs) in clinical trials.
The movement from paper-based to electronic PRO (ePRO) data collection has enhanced the integrity and accuracy of PRO data in clinical trials.
The US Food and Drug Administration has made it clear that electronic capture of clinical trial source data is preferred over paper-based data collection.
Gain Faster Closure, Lower Risk and Better Results with IBM EmptorisPerficient, Inc.
Procurement organizations are often challenged with lack of spend visibility, little-to-no automation around sourcing processes, difficulties in on-boarding, registering and measuring performance, and more. These organizations need to not only show value to the enterprise by reducing costs, but also provide value-added services to the business.
Sarah Radka, senior business consultant in Perficient’s IBM industry solutions practice, demonstrates how a leading international producer and marketer of beer, wine and spirits improved efficiency in the contract process by implementing a full IBM Emptoris solution.
During this webinar, our solution experts covered the keys to addressing critical contracting and supplier issues such as:
Streamlining procurement operations and removing bottlenecks
Providing and increasing overall spend visibility for an entire organization
Rationalizing and consolidating all templates into a standardized subset
Improving performance, attaining cost savings, mitigating risks and more
Digital Signatures: The Law and Best Practices for ComplianceCoSign by ARX
The CoSign Digital Signature solution automates your signature-based approvals compliantly and affordably, allowing you to cut costs and automate business processes.
Executing Validation of GxP Systems Electronically using SharePointMontrium
Executing Validation of GxP
Systems Electronically using
SharePoint
For more information on Montrium please visit:
- www.montrium.com
- www.twitter.com/Montrium
- www.youtube.com/Montrium
or email info@montrium.com
Importance of data standards and system validation of software for clinical r...Wolfgang Kuchinke
We present our evaluation of existing data standards for clinical trials. For this purpose a survey about the importance of data standards for clinical trials centers and EDC software companies were conducted. Electronic data capture in clinical trials uses a computerized system designed for the collection of clinical data in electronic form in Case Report Forms (CRF). It also covers medical data captured during clinical trials, safety data related to clinical trials, and patient reported outcome. The degree of implementation of standards, like CDISC ODM in available EDC software products was evaluated. Failure to establish data standards will make it difficult or impossible to connect data between different systems for efficient clinical study execution. The next step after purchasing a software solution is the computer system validation. Validation is about bringing computerized systems into regulatory compliance and making them compliant with GCP, GLP and GMP and other regulations (e.g. data protection). The basis standard for validation is provided by the GAMP Good Practice Guide, which provides a framework of best practices to ensure that computer systems are suitable for use and compliant with the legislation. The newest version uses a risk-based approach to computer system validation A system is evaluated and assigned to a predefined category based on its intended use and complexity. For validation one should define how all elements of the computer system are supposed to work (functional requirements), develop corresponding scripts and test routines to validate it is functioning as it should.
An audit trail in clinical research refers to a documented record of all activities and events related to the planning, conduct, and reporting of a clinical trial or research study. It provides a chronological and detailed account of actions taken, decisions made, and changes implemented throughout the course of the study. The primary purpose of maintaining an audit trail is to ensure the integrity, traceability, and transparency of clinical research data and processes. Here's a more in-depth look at the concept of an audit trail in clinical research:
Prioritizing Documentation for MDR Transition PlanningGreenlight Guru
This session will discuss the one year delay of the MDR date of application as well as some strategies to employ during the MDR Transition. In addition, some approaches for determining documents to prioritize for the transition will be discussed.
This session took place live at the Greenlight Guru True Quality Virtual Summit, a three-day event for medical device professionals to learn to get their devices to market faster, stay ahead of regulatory changes, and use quality as their multiplier to grow their device business.
Your next RIM solution - 3 key considerations for your moveV E R A
Considering to move to a new Regulatory Information Management system? Have a look at our pick of the 3 key considerations while moving to a new RIM system.
If you wish to receive more information - write us at info@cunesoft.com or visit our page https://cunesoft.com/en/products/rim/
Process Validation Master Planning DMAIC FusionGENEO
Process validation is a risk management verification activity for medical device and pharma companies. DMAIC is a well established methodology for improving process reliability, improving businesses and solving problems. This presentation discussed a logical fusion of these approaches. It includes a description of the validation life cycle. The business case for good validation is illustrated graphically. Contact us at ARVExcellence.com if you would like a copy.
ARV Excellence is a training and consulting firm based in Galway, Ireland with specialities in medical devices, and drug device combination product processes and process related problem solving
QMSR Harmonization: The Future of FDA's Quality Management System RegulationGreenlight Guru
Learn about the future of FDA's Quality Management System regulation.
This presentation originally aired during the 2022 Future of QMS Requirements Virtual Summit.
Improving Clinical Trial Performance: Part 3 - Streamline Trial Management wi...Veeva Systems
Henry Galio shares findings from the Unified Clinical Operations Survey and how research organizations can streamline trial management with Veeva Vault CTMS. Access the webinar > http://go.veeva.com/ModernCTMS
Agile Computer System Validation of software productsWolfgang Kuchinke
Personalized medicine seems to be a potential solution to the known challenges facing clinical research and drug development. To be employed in clinical research, software tools must undergo a process called Computer System Validation (CSV) for compliance with legal requirements and Good Clinical Practice (GCP). Four academic developer groups of the EU project p-medicine were surveyed to evaluate the readiness of their developed software products to be used for clinical research. The analysis of the survey showed that considerable gaps exist in tool maintenance, quality management and compliance documentation. Because all developer groups use agile development methods, recommendations for agile quality assurance were developed as well as for using agile methods to establish “compliance by design”. We show how agile validation can be established by small modifications of sprint processes.
ISO/IEC 27701 vs. ISO/IEC 27001 vs. NIST: Essential Things You Need to KnowPECB
Just a few days ago NIST published a complete refresh of the SP800-53, which provides a catalog of security measure to protect an organization against a variety of risks and threats.
How might NIST guidance fit in an information security management system like ISO/IEC 27001 and its privacy extension ISO/IEC 27701?
In this session, we will make a quick walk-through the standards and best practices, compare them, and find out how they map and differ from one another.
The webinar will cover:
• A quick recap of the topics covered in ISO27001/ISO27701
• Discovering the NIST guidelines for Information & cyber Security (SP800-SP1800)
• Main differences and mappings between NIST guidance and ISO27001
• About the latest publication (sep/2020) on NIST SP800-53 (Security and Privacy Controls for Information Systems and Organizations)
• Implementing information & cyber-security best practices
Date: October 14, 2020
YouTube presentation: https://youtu.be/zfsxSaaErqg
-------------------------------------------------------------------------------
Find out more about ISO training and certification services
Training: https://pecb.com/whitepaper/iso-27001-information-technology--security-techniques-information-security--management-systems---requirements
https://pecb.com/en/education-and-certification-for-individuals/iso-iec-27701
Webinars: https://pecb.com/webinars
Article: https://pecb.com/article
Whitepaper: https://pecb.com/whitepaper
-------------------------------------------------------------------------------
For more information about PECB:
Website: https://pecb.com/
LinkedIn: https://www.linkedin.com/company/pecb/
Facebook: https://www.facebook.com/PECBInternational/
Slideshare: http://www.slideshare.net/PECBCERTIFICATION
Strategies for Conducting GxP Vendor Assessment of Cloud Service Providers - ...Montrium
Want to deploy a new technology solution but not sure where to begin? These slides cover key considerations for choosing a vendor with cloud compliance and validation in mind. With the Office 365 subscription-based service gaining considerable momentum in the life sciences, it's important to stay ahead of the technological and regulatory curve and consider how an EDMS system will bring improvements to managing your GxP content.
Here we cover the following topics:
-Vendor assessment of Microsoft
-Subscription basics of Office 365
-Review of ISO/SOC audit reports
-Ensuring that no critical observations are made
-Security and quality controls in place
You can follow along with this presentation via webinar format:
https://info.montrium.com/strategies-for-conducting-gxp-vendor-assessment-of-cloud-service-providers
eCOA and ePRO and Their Use in Clinical Trials_pptxClinosolIndia
Virtual clinical trials are becoming even more popular because of technology advances. They offer enormous benefits to sponsors and patients. However, there are challenges. One of the key elements of a virtual clinical trial is ePRO and eCOA.
Patient-reported outcome (PRO) endpoints are often necessary to adequately evaluate the treatment benefit provided by new medical products (e.g., drugs) in clinical trials.
The movement from paper-based to electronic PRO (ePRO) data collection has enhanced the integrity and accuracy of PRO data in clinical trials.
The US Food and Drug Administration has made it clear that electronic capture of clinical trial source data is preferred over paper-based data collection.
Gain Faster Closure, Lower Risk and Better Results with IBM EmptorisPerficient, Inc.
Procurement organizations are often challenged with lack of spend visibility, little-to-no automation around sourcing processes, difficulties in on-boarding, registering and measuring performance, and more. These organizations need to not only show value to the enterprise by reducing costs, but also provide value-added services to the business.
Sarah Radka, senior business consultant in Perficient’s IBM industry solutions practice, demonstrates how a leading international producer and marketer of beer, wine and spirits improved efficiency in the contract process by implementing a full IBM Emptoris solution.
During this webinar, our solution experts covered the keys to addressing critical contracting and supplier issues such as:
Streamlining procurement operations and removing bottlenecks
Providing and increasing overall spend visibility for an entire organization
Rationalizing and consolidating all templates into a standardized subset
Improving performance, attaining cost savings, mitigating risks and more
Digital Signatures: The Law and Best Practices for ComplianceCoSign by ARX
The CoSign Digital Signature solution automates your signature-based approvals compliantly and affordably, allowing you to cut costs and automate business processes.
Digital Signature, Electronic Signature, How digital signature works, Confidentiality of digital signature, Authenticity of digital signature, Integrity of digital signature, standard of digital signature, Algorithm of digital signature, Mathematical base of digital signature, parameters of digital signature, key computation of digital signature, key generation of digital signature, verification of of digital signature
You might have heard about Cloud-Based Digital Signage and On-Premise Digital Signage. Both services are good it its own way. Choose which is best for you and start advertising today.
Alfresco: Implementing secure single sign on (SSO) with OpenSAMLJ V
Alfresco Summit 2013 (Barcelona and Boston)
This talk will provide an introduction to the OASIS SAML standard (Security Assertion Markup Language) and then describe in detail how we use OpenSAML to provide secure SSO to Alfresco Cloud in a multi-tenant environment, both in terms of Share and the core Repository. We will demonstrate the steps required for an Enterprise Network Admin to setup a trusted SAML connection ('circle of trust') to their chosen Identity Provider (IdP) such as Centrify, Ping Identity, ForgeRock OpenAM (formerly Sun OpenSSO) or potentially any other type of IdP that supports SAML v2.0. We will also discuss possible future requirements and improvements.
http://summit.alfresco.com/boston/sessions/implementing-secure-single-sign-sso-opensaml
http://www.youtube.com/watch?v=KroIZa1co6g
CoSign Digital Signatures: General Presentation Cisco
Complete, Standards-Based Turnkey Solution.
Any Business Process, Any Document, Record or Transaction for Desktops, Servers, and Cloud-Based Applications.
Crossing the Rubicon: Digital Signatures and Digital TransformationLarry Kluger
Digital signatures are the perfect tool for digital transformation of your organization. Open, standard digital signatures enable you to easily create truly paperless business processes. With digital signatures, your pdf's and other document types include the digital signature, there is no need to rely on a third signature company for signature verification. Your digitally signed pdf, itself, serves as your original document. Its signatures may be verified by using the free PDF Reader or other applications. Open digital signatures ensure no lock-in and full interoperability between signature applications from multiple vendors.
Sirius Decisions does a thorough review of DocuSign and its capabilities. This includes functionality, vision, support, best practices, etc. With signatures and transaction finalization becoming harder and harder, Sirius Decisions concludes that DocuSign with its focus on speed, accuracy, and cost is a viable and cost effective alternative to overnighting envelopes or faxing.
Document Management and Digitization solutions for medium sized EnterprisesTeamBreota
How to simply document management. The presentation describes document management and digitization solutions for medium sizes businesses and small businesses.
Digital Retail Africa 2023 hosted by IT News Africa - Carrie Peter speaks on Balancing User Experience and Security Compliance at Scale at the Digital Retail Africa 2023 conference. #retailtech #ecommerce #customerexperience #onlineshopping #securitycompliance
SharePoint, Nintex and DocuSign - Putting it all together Netwoven Inc.
“When Workflow Automation and Electronic Signature processes are combined, you have a very good thing.” – Mike Fitzmaurice, Nintex VP of Product Technology.
Incorporating electronic signatures ensures greater automation into existing forms and workflows. Learn the capabilities of Nintex, DocuSign and SharePoint and how the three can be integrated for greater collaboration.
Reach out to info@netwoven.com for more information!
Click on the link below to jumpstart your custom workflow solutions for FREE.
http://www.netwoven.com/13288-2/
This presentation explains Digital signature basics, how digital signatures help organisations. Digital signing makes processes efficient, electronic or digital signing is used by many Organisations to reduce costs, make processes effective, improve customer experience.
Digital Signatures in the Cloud: A B2C Case StudyiText Group nv
If you are a solution architect, or a business strategist new to digital signatures, this webinar will give you an overview of the components needed to build an end-to-end digital signature solution in-house, including PDF document workflows and document signing certificates.
About Alabama Graphics' history and the services offered such as: eDistribution, Bid Management, File Sharing Management, POD Printing on Demand, Online Fulfillment System, Onsite Facility Management, Wide Format Equipment, Large Format Graphics and Signage, DCX-Digital Color Graphics. Alabama Graphics has also been recognition as One of America’s Top 40 Printers.
A leading company with the vision to eliminate paper- based processes. Developing highly secure, qualified digital signature solutions, bringing efficiencies for corporates, enhancing security level while help saving the environment.
Similar to Implementing Digital Signatures in an FDA-Regulated Environment (20)
The world is quite a different place than it was six months ago, and with the 2020 holiday season fast approaching, the pressure is on to meet revenue goals in what’s been an uncertain year.
In August, we surveyed 154 marketing executives to find out what they think is likely to happen this holiday season and how they are preparing for it. The results are fascinating, and we’ve distilled them into clear actions you can take right now to adapt and prepare for a very different 2020 holiday season.
In this webinar, Eric Enge (Principal, Digital Marketing at Perficient) and Jim Hertzfeld (Chief Strategist, Digital at Perficient) discussed:
How marketers have already adapted and where they see the most opportunity moving forward
What will be different this holiday season and how to adjust your strategy accordingly
Ways to identify and meet changing customer expectations, wants, and needs
How to determine if your priorities or investments should change
What actions you can take right now to be successful
Transforming Pharmacovigilance Workflows with AI & Automation Perficient, Inc.
Medical information call centers have an opportunity to transform the way they capture, code, and analyze adverse events (AEs) and product quality complaints (PQCs) with artificial intelligence (AI) and automation.
The use of such innovative technology improves data quality and consistency, compliance, and operational efficiency. It helps reduce the frequency of your pharmacovigilance (PV) operations resources going home, saying, “I have more to do at the end of the day than I did when I started."
Our one-hour, on-demand webinar shows you how you can use AI and automation to turbo-charge your end-to-end PV system. Use cases and demonstrations will include:
Analyzing safety data
Auto-coding verbatim terms to official medical dictionary terms
Auto-creating an AE case in your database
Converting speech to text
The Secret to Acquiring and Retaining Customers in Financial ServicesPerficient, Inc.
Data, when leveraged effectively, can help you segment and target customers, analyze spending habits, and can create a personalized experience that builds value and customer loyalty.
Without a 360-degree view of your customers, you can’t properly target them with real-time personalized offers, advice, and other services. In addition, lack of customer intelligence creates lost opportunities for banks and insurers to cross-sell and upsell new products and services.
Our one-hour webinar covered how customer intelligence platforms can help you engage, acquire, and retain customers.
Oracle Strategic Modeling Live: Defined. Discussed. Demonstrated.Perficient, Inc.
The only thing certain about forecasting in a volatile economy is that the future is unpredictable. Historically, organizations have effectively utilized statistical techniques for short-term business planning, but leveraging actuals no longer allows us to predict the future. The ability to be prepared, responsive, and agile under these conditions is becoming a crucial success factor. Oracle Strategic Modeling can help you better navigate change to cope with uncertainty.
If your CFO’s questions regarding earnings, liquidity, and cash flow are unceasing and far-reaching, watch our on-demand webinar for a deep dive into strategic modeling. We modeled real-world scenarios to show how you can:
Quickly and easily develop a hierarchical model of your business
Leverage multiple pre-built functions to forecast key performance drivers
Provide transparency on forecasted financials via audit trail
Utilize goal seek to set financial targets and estimate the financials drivers necessary to achieve it
Perform sophisticated “what-if” analysis via simulations to improve the accuracy of your forecast
Use built-in dashboard functionality to deliver powerful reporting capabilities
While many stay-at-home orders have been lifted, consumers’ new digital buying behaviors and habits are here to stay. Watch our panel discussion on the accelerated need for commerce and learn how commerce and content can transform our digital economy.
Topics include:
-What is the “experience economy” and how do you leverage it? -If you move beyond product and price, what’s next?
-How business models have shifted and what you can do to break down silos and leverage new processes to capture the digital dollar.
-How organizations have built agile teams to address the ever-changing needs of customers, including responsive approaches that address the omnichannel consumer.
-Technologies that are best suited to enable your business and customers – and how headless commerce has changed the game.
-How the future of commerce is changing, and what you should do now to prepare.
Our panel features Jordan Jewell, IDC Research analyst known for his insight into the commerce industry. Joining him from Perficient is general manager Brian Beckham, who brings deep expertise in content management and empowering organizations in their digital transformations. Rounding out the panel is Episerver’s Joey Moore, who has spent the last decade helping organizations across the globe advance their digital maturity.
Centene's Financial Transformation Journey: A OneStream Success StoryPerficient, Inc.
Centene, a large multi-line managed care organization, was looking to modernize and streamline its corporate performance management (CPM) applications.
Centene had to move data between platforms multiple times during the close process so that close data could be fully consolidated and made available for reporting. This process had numerous challenges and inefficiencies that Centene wished to improve upon so that they could provide a more streamlined and more transparent process to the functional teams that leverage consolidated financials in their systems for reporting and analysis.
Centene chose OneStream XF for global and US consolidations, currency conversion, eliminations, and ownership percentage.
Michael Vannoni, director, financial systems solutions discussed the migration to OneStream XF including:
-Factors leading to the selection of OneStream XF
-Details of the solution design
-Benefits realized with global consolidation implementation
-Future planned enhancements
WHODrug Koda, developed by Uppsala Monitoring Centre (UMC), is an automated coding service, which uses artificial intelligence (AI) to automate the coding of drug names and ATC selections, improving consistency and operational efficiency. It can also be used to accelerate dictionary upgrades, including the transition from WHODrug B2 format to B3.
Through API (Application Programming Interface) web services, the coding engine can be integrated with custom or off-the-shelf drug safety, medical coding, or data management systems.
In this webinar, Perficient and UMC discussed WHODrug Koda and how you can integrate it into your medical coding activities.
Preparing for Your Oracle, Medidata, and Veeva CTMS Migration ProjectPerficient, Inc.
There are multiple reasons why companies migrate to a new clinical trial management system (CTMS). Still, the two most common are mergers and acquisitions (i.e., CTMS consolidation) and the desire to switch CTMS vendors. Regardless of the reason, many of the best practices, processes, and tools are the same.
In this webinar, we looked at the migration approaches taken across several case studies. You’ll come away with an understanding of:
Pros and cons of each CTMS migration method
Types of migration tools, including APIs, ETL tools, and adapters
Approximate timelines and costs associated with each migration method
The topics discussed in this webinar can be applied to any CTMS migration project, whether you’re moving to or from Oracle’s Siebel CTMS, Medidata’s Rave CTMS, and Veeva’s Vault CTMS.
Accelerating Partner Management: How Manufacturers Can Navigate Covid-19Perficient, Inc.
The pandemic has ushered in a new normal for manufacturers, and the impact of digital communication is more important than ever.
View our on-demand webinar with Tony Kratovil, Regional Vice President of Manufacturing at Salesforce, and Eric Dukart, National Sales Executive at Perficient. They covered why the right digital strategies are critical for manufacturers in the wake of COVID-19.
Our webinar covered:
Current challenges with forecasting, collaboration, and disruptions to distribution networks.
Insights for stabilizing operations, accelerating partner management, and developing a digital strategy that differentiates your business.
Candid Q&A with real-world examples.
New Work.com resources to help manufacturers restart safely and rebuild.
Tools and resources to move forward – fast.
The Critical Role of Audience Intelligence with Eric Enge and Rand FishkinPerficient, Inc.
Things move quickly in marketing. How do you identify what your customers need and how you can help? Now more than ever, audience intelligence is the key.
Audience intelligence is about understanding your target customers, their needs, what resonates with them, and how you can reach them. Eric Enge (Digital Marketing Principal, Perficient) and Rand Fishkin (Co-Founder & CEO, SparkToro) discussed this topic live on May 7, 2020. Watch to hear tactics for gaining a better understanding of your customers, how to use audience intelligence to optimize your marketing now, and more.
Cardtronics, the global leader in ATM deployment and management, decided to retire its on-premises Hyperion solution to gain the operational efficiencies, features, and functionality provided by a best-in-class cloud solution.
Cardtronics chose Oracle EPM Cloud including Financial Consolidation and Close, Planning, Management Reporting, Account Reconciliation, Enterprise Data Management, as well as Oracle Analytics Cloud.
In this video, project owner Richard Ng, director, financial systems, Cardtronics, discusses the migration to Oracle EPM Cloud including:
Multi-release 18-month deployment schedule across multiple countries
Benefits of a global Chart of Accounts for ERP and EPM
Seamless integration across ERP Cloud, HCM Cloud, and EPM Cloud
Preparing for Project Cortex and the Future of Knowledge ManagementPerficient, Inc.
Microsoft has turned traditional enterprise content management on its head with its recent announcement of Project Cortex.
Project Cortex uses advanced artificial intelligence to harness collective knowledge from across the enterprise and automatically organize it into shared topics like projects, products, processes, and customers. Using AI, Cortex creates a knowledge network based on relationships among topics, content, and people and delivers it in the apps you use every day – Office, Outlook, and Teams.
This webinar examined Project Cortex in more detail, including:
• What is Project Cortex?
• Why is Project Cortex different than other knowledge network projects previously introduced?
• How does incorporating AI and automation change the game?
• What is possible with Project Cortex?
• What can you do to prepare?
Utilizing Microsoft 365 Security for Remote Work Perficient, Inc.
With an increasingly mobile workforce, and the spread of shadow IT, the rapid rise of cybercrime - companies must find unique ways to effectively manage their sprawling SaaS portfolio.
LF Energy Webinar: Electrical Grid Modelling and Simulation Through PowSyBl -...DanBrown980551
Do you want to learn how to model and simulate an electrical network from scratch in under an hour?
Then welcome to this PowSyBl workshop, hosted by Rte, the French Transmission System Operator (TSO)!
During the webinar, you will discover the PowSyBl ecosystem as well as handle and study an electrical network through an interactive Python notebook.
PowSyBl is an open source project hosted by LF Energy, which offers a comprehensive set of features for electrical grid modelling and simulation. Among other advanced features, PowSyBl provides:
- A fully editable and extendable library for grid component modelling;
- Visualization tools to display your network;
- Grid simulation tools, such as power flows, security analyses (with or without remedial actions) and sensitivity analyses;
The framework is mostly written in Java, with a Python binding so that Python developers can access PowSyBl functionalities as well.
What you will learn during the webinar:
- For beginners: discover PowSyBl's functionalities through a quick general presentation and the notebook, without needing any expert coding skills;
- For advanced developers: master the skills to efficiently apply PowSyBl functionalities to your real-world scenarios.
Epistemic Interaction - tuning interfaces to provide information for AI supportAlan Dix
Paper presented at SYNERGY workshop at AVI 2024, Genoa, Italy. 3rd June 2024
https://alandix.com/academic/papers/synergy2024-epistemic/
As machine learning integrates deeper into human-computer interactions, the concept of epistemic interaction emerges, aiming to refine these interactions to enhance system adaptability. This approach encourages minor, intentional adjustments in user behaviour to enrich the data available for system learning. This paper introduces epistemic interaction within the context of human-system communication, illustrating how deliberate interaction design can improve system understanding and adaptation. Through concrete examples, we demonstrate the potential of epistemic interaction to significantly advance human-computer interaction by leveraging intuitive human communication strategies to inform system design and functionality, offering a novel pathway for enriching user-system engagements.
DevOps and Testing slides at DASA ConnectKari Kakkonen
My and Rik Marselis slides at 30.5.2024 DASA Connect conference. We discuss about what is testing, then what is agile testing and finally what is Testing in DevOps. Finally we had lovely workshop with the participants trying to find out different ways to think about quality and testing in different parts of the DevOps infinity loop.
Kubernetes & AI - Beauty and the Beast !?! @KCD Istanbul 2024Tobias Schneck
As AI technology is pushing into IT I was wondering myself, as an “infrastructure container kubernetes guy”, how get this fancy AI technology get managed from an infrastructure operational view? Is it possible to apply our lovely cloud native principals as well? What benefit’s both technologies could bring to each other?
Let me take this questions and provide you a short journey through existing deployment models and use cases for AI software. On practical examples, we discuss what cloud/on-premise strategy we may need for applying it to our own infrastructure to get it to work from an enterprise perspective. I want to give an overview about infrastructure requirements and technologies, what could be beneficial or limiting your AI use cases in an enterprise environment. An interactive Demo will give you some insides, what approaches I got already working for real.
Essentials of Automations: Optimizing FME Workflows with ParametersSafe Software
Are you looking to streamline your workflows and boost your projects’ efficiency? Do you find yourself searching for ways to add flexibility and control over your FME workflows? If so, you’re in the right place.
Join us for an insightful dive into the world of FME parameters, a critical element in optimizing workflow efficiency. This webinar marks the beginning of our three-part “Essentials of Automation” series. This first webinar is designed to equip you with the knowledge and skills to utilize parameters effectively: enhancing the flexibility, maintainability, and user control of your FME projects.
Here’s what you’ll gain:
- Essentials of FME Parameters: Understand the pivotal role of parameters, including Reader/Writer, Transformer, User, and FME Flow categories. Discover how they are the key to unlocking automation and optimization within your workflows.
- Practical Applications in FME Form: Delve into key user parameter types including choice, connections, and file URLs. Allow users to control how a workflow runs, making your workflows more reusable. Learn to import values and deliver the best user experience for your workflows while enhancing accuracy.
- Optimization Strategies in FME Flow: Explore the creation and strategic deployment of parameters in FME Flow, including the use of deployment and geometry parameters, to maximize workflow efficiency.
- Pro Tips for Success: Gain insights on parameterizing connections and leveraging new features like Conditional Visibility for clarity and simplicity.
We’ll wrap up with a glimpse into future webinars, followed by a Q&A session to address your specific questions surrounding this topic.
Don’t miss this opportunity to elevate your FME expertise and drive your projects to new heights of efficiency.
Smart TV Buyer Insights Survey 2024 by 91mobiles.pdf91mobiles
91mobiles recently conducted a Smart TV Buyer Insights Survey in which we asked over 3,000 respondents about the TV they own, aspects they look at on a new TV, and their TV buying preferences.
UiPath Test Automation using UiPath Test Suite series, part 3DianaGray10
Welcome to UiPath Test Automation using UiPath Test Suite series part 3. In this session, we will cover desktop automation along with UI automation.
Topics covered:
UI automation Introduction,
UI automation Sample
Desktop automation flow
Pradeep Chinnala, Senior Consultant Automation Developer @WonderBotz and UiPath MVP
Deepak Rai, Automation Practice Lead, Boundaryless Group and UiPath MVP
Builder.ai Founder Sachin Dev Duggal's Strategic Approach to Create an Innova...Ramesh Iyer
In today's fast-changing business world, Companies that adapt and embrace new ideas often need help to keep up with the competition. However, fostering a culture of innovation takes much work. It takes vision, leadership and willingness to take risks in the right proportion. Sachin Dev Duggal, co-founder of Builder.ai, has perfected the art of this balance, creating a company culture where creativity and growth are nurtured at each stage.
Builder.ai Founder Sachin Dev Duggal's Strategic Approach to Create an Innova...
Implementing Digital Signatures in an FDA-Regulated Environment
1. Implementing Digital Signatures in anFDA-Regulated EnvironmentMichelle Engler, Senior Application Architect, Life Sciences, Perficientwith support from Sally Miranker, Computer System Validation, Life Sciences, PerficientTina Howard, Quality Assurance-Compliance, Life Sciences, Perficient
facebook.com/perficient
twitter.com/Perficient_LS
linkedin.com/company/perficient
2. 2
Perficient is a leading information technology consulting firm serving clients throughoutNorth America and Europe.
We help clients implement business-driven technology solutions that integrate business processes, improve worker productivity, increase customer loyalty and create a more agile enterprise to better respond to new business opportunities.
About Perficient
3. 3
•Founded in 1997
•Public, NASDAQ: PRFT
•2013 revenue $373 million
•Major market locations:
•Allentown, Atlanta, Boston, Charlotte, Chicago, Cincinnati, Columbus, Dallas, Denver, Detroit, Fairfax, Houston, Indianapolis, Minneapolis, New York City, Northern California, Oxford (UK), Philadelphia, Southern California, St. Louis, Toronto, Washington, D.C.
•Global delivery centers in China and India
•>2,200 colleagues
•Dedicated solution practices
•~90% repeat business rate
•Alliance partnerships with major technology vendors
•Multiple vendor/industry technology and growth awards
Perficient Profile
4. Business Process Management
Customer Relationship Management
Enterprise Performance Management
Enterprise Information Solutions
Enterprise Resource Planning
Experience Design
Portal / Collaboration
Content Management
Information Management
Mobile
BUSINESS SOLUTIONS
50+ PARTNERS
Safety / PV
Clinical Data Management
Electronic Data Capture
Medical Coding
Clinical Data Warehousing
Clinical Data Analytics
Clinical Trial Management
Healthcare Data Warehousing
Healthcare Analytics
CLINICAL / HEALTHCARE IT
Consulting
Implementation
Integration
Migration
Upgrade
Managed Services
Private Cloud Hosting
Validation
Study Setup
Project Management
Application Development
Software Licensing
Application Support
Staff Augmentation
Training
SERVICES
5. 5
Michelle Engler, Senior Solutions Architect
Life Sciences, Perficient
(650) 291-4710
Michelle.Engler@perificient.com
Sally Miranker, Head of Computer Systems Validation
Life Sciences, Perficient
(619) 980-7288
Sally.Miranker@perificient.com
Tina Howard, Head of Quality Assurance Compliance
Life Sciences, Perficient
(760) 696-3650
Tina.Howard@perificient.com
Welcome & Introduction
6. Agenda
•Digital Signature Technology Overview
•Requirements for a dSignatureSolution
•Available dSignatureSolutions
•dSignatureSolution and 21 CFR Part 11 Compliance
•Implementing, Validating, and Releasing the dSignatureSolution
•Demonstration
•Future Plans
•Questions
•Contact Information
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7. Digital Signature Technology Overview
Electronic Signatures and Digital Signatures
•Definitions
FDA 21 CFR 11.3 (7) -Electronic Signature
The term 'electronic signature' means an electronic sound, symbol, or process, attached to or logically associated with a contract or other record and executed or adopted by a person with the intent to sign the record
•FDA 21 CFR 11.3 (5) -Digital Signature
Digital signature means an electronic signature based upon cryptographic methods of originator authentication, computed by using a set of rules and a set of parameters such that the identity of the signer and the integrity of the data can be verified
A digital signature falls into a sub-group of electronic signatures that provides the highest levels of security and universal acceptance. Digital signatures are based on Public Key Infrastructure (PKI) technology, and guarantee signer identity and intent, data integrity, and the non-repudiation of signed documents.1
1. http://www.arx.com/learn/about-digital-signature/digital-signature-faq
7
8. Digital Signature Technology Overview
What is a digital signature?
•Adigital signaturetakes the concept of traditional paper-based signing and turns it into an electronic “fingerprint.” This “fingerprint,” or coded message, is unique to both the document and the signer and binds them together.
•Digital signatures ensure the authenticity of the signer.
•Any changes made to the document after it has been signed invalidate the signature, thereby protecting against signature forgery and information tampering.
Is a digital signature legally enforceable?
•Yes. In 1999, the EU passed the “EU Directive for Electronic Signatures” and on June 30, 2000, President Clinton signed the Electronic Signatures in Global and National Commerce Act (“ESIGN”), which made signed electronic contracts and documents as legally binding as a paper-based contract. Today, digital signature (standard electronic signature) solutions carry recognized legal significance, enabling organizations to comply with regulations worldwide. 8
9. Business Case for Digital Signatures - Survey Compliance and Assumptions
9
•Survey Monkey was utilized to create a survey to assess the business need and results were able to be compiled from 53 respondents
•Perficient-Life Sciences processes approximately 856 signatures for the 53
•Time to print, sign, scan, upload, and mail original document to headquarters for each signatory was estimated and calculated company-wide
•Time to execute a digital signature was estimated at 5 minutes per signature
•Anticipated time/resource savings is approximately 75% or 314 hours/month
Unaccounted for variables: signer’s location (for mailing), equipment limitations, cost of materials (e.g. paper, printer ink), and management of hard copies of documents
10. Business Case for Digital Signatures - Department Signatures Per Month
10
12. Perficient-Life Sciences Requirementsfor a Digital Signature Solution
12
•Support third-party Applications (Word, Excel, PDF)
•Allow for multiple signatures per document
•Allows for sectional signing (MS Word)
•Has audit trail and secured time stamps
•Allows for sequential and parallel signing workflow
•Receives instant alerts when someone signs
•Integrates with our EDMS (Alfresco)*
•Compliant with 21 CFR Part 11
•Integrates with Active Directory and requires username/password for signing
•Provides phone/email support
•System is easy and intuitive to use
•System has trial period
•System is available in the cloud**
* No solutions were able to integrate directly out-of-the-box with our Alfresco environment; hence, this requirement was adjusted to require the ability to integrate systems via a development API
** Later, we determined that having a system in the cloud introduced more risk than having a local installation of the solution basedoncontrol of the environment
13. Digital Signature SolutionsResearched and Reviewed
13
DocuSign*
•Cloud-based only
•Cost determined on number of signatures executed
•Extensive full routing and signing certificates available
•Utilized in many other industries
•Several configuration options available
•Only signs PDF
•Adequate support available
•Electronic Signatures
•Full Web API for EDMS integration available
AssureSign*
•Client or cloud-based solution available
•Cost determined by number of signers
•Full routing available
•Uses templates for signing
•Only signs PDFs
•Adequate support available
•Digital Signatures
•Full Web API for EDM Integration available
Signadura*
•Least expensive solution
•Not fully translated to English
•Support was provided from Spain
•Only signs PDFs
•Digital Signatures
•Integrated with Alfresco
ARX CoSign*
•Client or cloud-based solution available
•Cost determined by number of signers
•Routing available when integrated with EDMS
•Signs PDFs, MS Word, or MS Excel documents
•Experienced with Life Sciences and 21 CFR Part 11 Compliance
•Cost was competitive with other solutions
•Adequate support available
•Digital Signatures
•Full Web API for EDMS integration available
Adobe EchoSign
•Most expensive solution available
•Ruled out based on existence of lower cost options
* Demonstration completed by vendor for solution
14. Digital Signature Solution – Selection of ARX CoSign
•ARX CoSignSelected
–Client based installation with installed, unconfiguredappliance provided by ARX
–Allows for signing of all types of documents
–Integration with SharePoint available and full Web Developers API available
–Provides for client software or signing via a web browser
–Allows prepping of documents for signature
–Adequate support available and provided
–Cost-effective solution that provides Perficient-Life Sciences employees/consultants with the ability to sign documents
–Opportunity for Perficient–Life Sciences to become an implementation expert for digital signature solutions for our clients
14
18. Implementing and Validating the Digital Signature Solution
•Receive, install, and configure CoSign Appliance
•Install and configure CoSign Web Application (separate web server)
•Add CoSign User and Administrator Groups to Active Directory
•Determine how the system can be used for existing documents
–Updated signature block of document templates
–Meaning of signature added to signature block of document templates
•Prepare and execute full validation for the system:
–Validation Plan
–User Requirements Specification (URS)
–User Requirements to Performance Qualification Traceability Matrix
–Installation Qualification (IQ) Protocol
–Installation Log
–IQ Test Suite
–IQ Summary Report
–Performance Qualification (PQ) Protocol
–PQ Test Suite
–PQ Summary Report
–Validation Summary Report with Statement of Validation
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19. Implementing and Validating the Digital Signature Solution (continued)
•Create Supplemental Guidelines and Guides
–CoSignClient User Guideline
–CoSignWeb Application User Guideline
–CoSignAdministrator Guide
•Create New Application Roles
–CoSignSuper User Role
–CoSignUser Role
•Create Training Materials
–CoSignOverview
–Training on CoSignClient (video and presentation)
–Training on CoSignWeb Application (video and presentation)
•Update existing SOP-001 Controlled Documents procedure to allow for digital signatures
•Send letter of non-repudiation to FDA to inform them of our use of digital signatures
19
20. Releasing the Digital Signature Solution
•Perficient-Life Sciences Support Representative trained on Tier 1 support
•Internal bug tracking system updated to accept issues/questions with the implementation of CoSign
•Controlled Document Required Training Notification sent
•Supplemental training provided as video, live session, and with presentations
•Rolling release implemented for users that have completed required training
•Installation support provided to those users that have completed training and require the CoSign Client
•Solution Released in August 2014
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21. Future Plans
•Use ARX CoSign MS Word “Sectional Signing” to allow completion of test cases electronically
•Create a connector between ARX CoSignand the Perficient-LS EDMS, Alfresco Community Edition
•Provide implementation and validation services for Life Sciences companies wishing to implement ARX CoSign
21