The life sciences industry is undergoing a digital transformation. As legacy IT systems move to the cloud, an effective transition strategy is required. Hear how Box is enabling 800+ Life Sciences organizations transition and manage their existing content infrastructure to cloud content management. The discussion will highlight popular use cases being deployed on Box and how Life Sciences companies are navigating through this transformation.
In this webinar we covered:
- Typical steps on how customers are adopting Box cloud content management
- A customer case study on how Box is speeding up their sales process
- Extending Box content into 3rd party applications
Standard compute platforms are indispensable in the industry, however deploying and monitoring these platforms can be time consuming and cumbersome. Please join Peter Lutz from Dimension Data for a discussion on how to rapidly deploy these platforms while still meeting compliance requirements.Read more >
Leading pharmaceutical manufacturers and clinical research organizations are investing in digital operations across the development and commercialization spectrum to improve efficiency, accuracy, and trust when bringing new products to market.
Watch this on-demand webinar to hear from digital trailblazers and adopt best practices to ensure that your organization is collaborating effectively and building a safe global trust network for digital success.
Topics covered include:
• Applications for digital transactions and signatures
• Identity management
• High impact regulated use cases
• Compliance with global and industry regulations
• Best practices for digital adoption
Watch and learn how Documentum Research and Development (R&D) and Documentum Submission, Store and View (SSV) ensures alignment with global regulatory guidance to speed submissions.
Listen as Lena Shafir, Product Manager, Life Sciences Regulatory Solutions, provides an overview of recent enhancements to Documentum Research and Development (R&D) and Documentum Store and View (SSV). She’ll also cover how our latest release (4.2) delivers lifecycle support for medical device documentation and ensures alignment with global regulatory guidance to speed submissions.
The healthcare landscape is rapidly changing as it responds to a multitude of well-known issues. Coupled with emerging digital technologies, these drivers are shaping the industry, moving it towards a more sophisticated, outcomes-driven model that demands a new approach. The new world emerging is one in which value is defined, created and evaluated in a very different way, with marketing playing a critical role.
On 30 November, EY (a global leader in assurance, tax, transaction and advisory services) in association with PMGroup, will host a free webinar debating the future of marketing in Life Sciences. Is your function fit for purpose?
Good data is the key to innovation, solid research collaboration, and, ultimately, the creation of life-saving drugs and treatments.
But does your IT strategy reflect this? All too often, data is compromised and constrained by the needs of your enterprise’s applications. Join our webinar to discover a new data-centric approach to IT that's radically changing the biggest names in life sciences.
By moving to a data-centric model, your organization will be better poised to:
•Integrate data regardless of source, volume, and variation
•Quickly and easily change out applications
•Uncover unique insights
Gary Palgon, CISSP and VP, Healthcare and Life Sciences at Liaison, will demonstrate how to apply this innovative data-centric approach in a life sciences environment.
In an age when blockbusters are few and far between, pipeline acceleration and performance are the key to bottom-line profits. Where will you find the immediate savings you need in time and money?
Watch this on-demand webinar to learn 10 ways to reduce cycle time and development costs with a fully digital solution. Topics covered include:
-Top life sciences use cases
-21 CFR Part 11 capabilities
-Best practices for digital adoption
-Global scalability and compliance
-Industry and validation partners
In this recorded webinar, you’ll hear Mike Porco, Manager Service Solutions at Pacific Life, talk about the value of using Blazent—with its tight integration with ServiceNow—to build quality IT data.Read more >
The second part of the two-part series on the US Federal Life Sciences market focuses on the two of three EMC pillars: IT Transformation and Trust. The architecture and infrastructure that has powered the faster-than-Moore's-Law growth in Life Sciences, specifically Genomics will be presented along with Trust. Trust, and not technology is the singular issue that will determine the progress of Genomics into the practice of Precision Medicine.Read more >
Fueled by the life-changing technologies of genomic sequencing, genotyping, gene expression analysis, and bioinformatics, Life Sciences organizations are experiencing intense growth in data. Life Sciences researchers are generating massive amounts of data with storage retention requirements from two years minimum to perpetuity. The technologies and tools driving biomedical research and drug development such as next generation sequencing (NGS), genomic analysis, proteomics, and high content screening (HCS) also pose immense challenges to managing data throughout the data lifecycle - from generation, to analysis, to archive.Read more >
Watch and discover the five essential best practices for implementing an electronic document management system for Life Sciences organizations.Read more >
Watch this on-demand webinar to learn how you can get to market sooner with simple, secure, and fully digital workflows using DocuSign – and how you can do so in accordance with Part 11 regulations.Read more >
As the molecular profiling Caris Life Sciences performs for cancer patients has advanced, the company’s needs for managing high-performance analytics and storage have grown exponentially. Its next-generation sequencing (NGS) processes are now fully supported by IBM supercomputing technologies, including processing by IBM NeXtScale System servers.Read more >
To quickly bring life-saving therapies to market, the drug development process relies on secure collaboration across the extended enterprise. However, organizations find that today's legacy content management systems lead to silos between their regulated and unregulated content.
With Box GxP Validation, pharma and life sciences companies can now validate Box so they can collaborate on, manage and distribute regulated clinical, lab and manufacturing content in Box. That means all of your content is standardized on a single content platform that meets regulatory and compliance standards, so you can eliminate inefficient silos, enable seamless collaboration and accelerate the validation process.
Join our upcoming webinar to learn how to:
- Leverage Box for your GxP content — such as collaborating with CROs — and consolidate expensive GxP-specific systems
- Cut validation time in half and save up to 75% in validation costs with always-on testing
- Meet CFR Part 11 requirements by integrating Box with e-signature providers, such as DocuSign
Hear about this new game-changing model for maintaining GxP compliance in the cloud with Riju Khetarpal, Life Sciences Managing Director at Box, and Manu Vohra, VP of Content Management at USDM Life Sciences.
La tecnología está transformando nuestra sociedad pero trae consigo varios retos. Abundan las noticias falsas, hay un crecimiento del uso de chatbots y una preocupación por la seguridad de los datos. En ese entorno ¿cómo las marcas pueden construir y mantener la confianza de los consumidores?
Participa el próximo 16 de noviembre en el webinar de Connected Life, Hidden dangers: Trust in a Connected World.
- ¿La conectividad está mejorando las relaciones con los clientes?
- ¿Qué impacto tienen los chatbot en el servicio al clientes?
- ¿Cómo pueden generar las marcas nuevas oportunidades de eCommerce al hacer frente a los desafíos de la pérdida de confianza?
Dr Lisa Haile presents this webinar exploring issues and strategies for diagnostic and therapeutic patents and licenses.
This webinar will address questions such as:
Are diagnostic tests patentable?
What are the effects of the Alice ruling and the Myriad Genetics case on patents?
What strategies can be used to avoid the pitfalls associated with patenting around "laws of nature"?
What are the latest rulings and precedents around diagnostics and genetic markers and how is the landscape evolving?
This is essential viewing for anyone involved with intellectual property and innovation in the life sciences sector.
The process of buying life insurance and receiving post-issue service is becoming increasingly digitized – driven by customer expectations for convenience and ease. Electronic signatures are enabling this digital transformation.
In response to the accelerated adoption, Celent recently published the report, “Putting a Lock On Straight-Through Processing – Life Insurance E-Signature Vendors 2017”. The research aimed to answer the questions: “how is e-signature technology transforming the life insurance customer experience”; “who are the main vendors?”; and “what are the common components of a solution?”.
The answers to these questions are shared in this on-demand webcast, hosted by LOMA. Watch it to learn what to look for in a solution, hear an update on how the vendor landscape has changed and takeaway these highlights:
Top e-signature solution requirements
How to evaluate and differentiate vendors
Perceived and real obstacles to continued adoption
E-Signature Case Studies in Life Insurance
- Colleen Risk, Senior Analyst - Celent
- Andrea Masterton, Director Corporate Marketing - eSignLive by VASCO
Senior level expert panel debate on the likely impacts of a hard v soft Brexit for life sciences companies in Britain.Read more >
The #1 question for people everywhere:
How to design & deliver a work-life balance that maximizes our best efficiencies at work and our most meaningful life outside work?
George Kinder has specialized in delivering work-life balance to consumers and professionals worldwide through Life Planning and Mindfulness trainings and workshops for 30 years.
The world today requires commitments in more areas than ever before. The requirements for work have been continuously expanded with new daily technologies, constantly competing with family time and lifestyle choices. Balancing a healthy lifestyle is critical for the future success of everyone in the workforce today.
Combining thoughtful financial Life Planning with Mindfulness delivers work-life balance to everyone. Mindfulness gives you the ability to recognize where you sacrifice your work-life balance. Life Planning defines the balance you really want and the financial elements needed to secure it. Join this webinar and learn how to design the best of lives for yourself, your employees or your clients that simultaneously maximizes efficiencies at work.
You will learn:
1.How to deliver work-life balance to yourself, your clients and your employees
2.How Mindfulness & Life Planning are key elements to your work-life balance
3.Learn how to begin the process of creating a financial Life Plan to support your work-life balance
4.Strategies for finding more time to support a good work-life balance
Can’t Miss Takeaways - You will:
1.Do the famous GK 3-Questions facilitated by George Kinder
2.See and receive access to a Free consumer Life Planning website
3.Receive a Free “Life Planning for You” book by George Kinder
4.Have access to an audio guide to a daily Mindfulness practice.
Who should attend?
Anyone seeking to improve their personal work-life balance or to help their clients or employees improve their work-life balance.
Life sciences industry is undergoing a major transformation. The growing number of FDA approved targeted therapies on one-side and an increasing number of pay-for-performance deals between big pharma and payers signals the dawn of value-based precision medicine. Clinical trials are no longer limited to data snapshots gathered during trial site visits. Real-time data streaming from wearables enable remote patient monitoring during trials and beyond. Aggregating patients RWD (Real World Data) such as health information from EMRs, genomics, wearables, and mobile apps can enable advanced data analytics for R&D and commercial use cases.Read more >
ICTFOOTPRINT.eu is organising its 5th webinar on 27th April 2017, 12:00 CEST to help you manage the energy consumed by ICT and know how Life Cycle Assessment (LCA) can guide you to make your ICT more sustainable. All those who want to become more sustainable in ICT are welcome to join us in this exciting webinar.
Jean-Marc Alberola, Group Energy Strategy leader at Airbus & Vice Chairman of ETSI ISG OEU (Industry Specification Group Operational Energy Efficiency For Users). Jean-Marc will speak about the work developed by ETSI ISG-OEU, operative KPIs that enable the monitoring of the energy management performance in data centres and ICT sites. After a short description of the global KPI DCEM, the presentation will focus on the implementation of these KPI’s in an industrial area of corporate ICT sites.
Fadri Casty & Tereza Lévová, both from EcoInvent, , the world's most consistent & transparent Life Cycle Inventory database. The ecoinvent database provides well documented process data for thousands of products, helping you make truly informed decisions about their environmental impact. Fadri and Tereza will demonstrate the value of doing LCA on ICT equipment.
Berina Delalic, from multEE will introduce the Monitoring & Verification Platform (MVP), a web based tool developed to calculate and store data about energy and CO2 savings resulting from implemented energy efficiency measures. Having in mind central role of ICT especially in the commercial sector, some methods are developed for improving ICT’s energy efficiency, and therefore achieving CO2 emission reduction. The presentation will show how MVP can be used for measuring results from the activities that enable more efficient use of energy for ICT in commercial buildings.
The webinar will be moderated by Silvana Muscella (Project Coordinator of ICTFOOTPRINT.eu and CEO of Trust-IT Services) who has broad experience in stimulating topics in the ICT sector.
During the weekly webinar series Technology Tuesdays, LeClair Group's insurance analyst Margaret Lett, Ph.D., shares tips with insurance advisors on how to navigate and take advantage of the Advisor tools provided on LeClair Group's Advisor Advantage website. During the webinar Margaret, with the assistance of LeClair Group's Life Insurance product expert Bob Hertz, will demonstrate how to use iGo with Life Insurance products on the LeClair Group's Advisor Advantage website.iGO is a fillable form and data gathering solution that is designed to streamline and accelerate the selling of Life Insurance insurance. iGO enables career and independent producers to improve efficiency and productivity by eliminating errors and producing 100% in Good Order submissions.Read more >
During Technology Tuesdays,LeClair Group's insurance analyst Margaret Lett, will share more tips for insurance advisors. This week the topic will be the Term Life quote engine that is available to licensed insurance advisors.Read more >