Delaying the onset of aging via rejuvenated stem cell responses

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Professor Irina Conboy, PhD Department of Bioengineering, UC Berkeley
Delaying the onset of aging via rejuvenated stem cell responses
May 12 2009
47 mins
Delaying the onset of aging via rejuvenated stem cell responses
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  • The 4 C's for Using Cloud to Support Scientific Research Recorded: May 19 2015 46 mins
    Jeff Tabor & Scott Jeschonek
    While cost is a primary "c" driving the adoption of object-based cloud solutions in the life sciences, compute, capacity, and collaboration may all be bigger incentives. In this webinar, we'll examine how to use an Avere Hybrid Cloud NAS infrastructure to gain big benefits in areas like genomics research, personalized medicine, drug discovery, imaging, and other data analysis applications.

    • Compute - Building production environments in the compute cloud without rewriting existing applications

    • Capacity - Modernizing storage archives and disaster recovery by adding object storage for durability while leveraging existing on-premises NAS

    • Collaboration - Using the cloud t o safely and securely share data globally

    • Cost - Using cloud to lower overall costs to keep pace with fast-growing demands of research initiatives
  • Healthcare Analytics in a Disconnected World Recorded: Mar 18 2015 44 mins
    Sven Junkergård, CTO, Zephyr Health
    Some of the most critical data required to solve analytical problems in the healthcare and life sciences world lack the type of keys that we rely on so heavily in other domains. This session will focus on solutions to the fundamental data connectivity challenges in this area and how to enable impactful analytics on a few high value but disconnected healthcare data sources.
  • Compliance Does Not Equal Security – A Risk-Based Plan for ePHI Protection Recorded: Aug 20 2014 63 mins
    Andrew Hicks, Healthcare Practice Director at Coalfire; and Mark Bower, VP Product Mgt, Voltage Security
    With the emergence of big data healthcare analytics, electronic health information exchange, clinical data warehousing, and other technologies for optimizing patient care, the healthcare industry has never been more reliant on electronic data and the strict requirements associated with the data. The advances in business processes, technology and regulations require that data security initiatives evolve to address new and growing threats. Coincidentally, in a recent survey, 69% of organizations felt that provisions of the Affordable Care Act (ACA) have the effect of increasing or significantly increasing risks to patient privacy and security.

    Chasing compliance is an expensive proposition that doesn’t adequately address the current security threats and vulnerabilities. Organizations that simply want to comply with the regulations are already at risk. A more effective program is risk-based -- one where incremental changes to controls can be made in real-time to more effectively combat current threats to your security program. Join us for this webinar where you’ll learn:

    - Why compliance is an outcome of an effective data protection program.
    - Risk assessment, analysis and management – what’s the difference and why you need them.
    - What is considered ‘reasonable’?
    - What leading healthcare organizations are doing today to protect data, with a focus on securing Big Data for healthcare analytics?
    - How data protection can help without getting in the way of patient care.
    - How do you protect from your healthcare organization public loss of confidence?
  • Demonstrating the Value of Sustainable Health Info. Exchange Recorded: Apr 7 2010 35 mins
    Rodney Cain, CIO, HealthBridge
    HealthBridge is a nationally recognized Health Information Exchange based in Cincinnati Ohio that has been in operation since 1997 and is regularly cited as an example of a financial sustainable HIE effort. Rodney Cain, Chief Information Officer will discuss the history and development the HealthBridge with a focus on strategies and lessons learned over the years as the chief technology architect of the HIE effort with an eye to the future and the impacts of HITECH and Meaningful Use.

    HealthBridge has grown to a nationally recognized HIE that includes 24 hospitals and over 5000 physicians in Ohio, Indiana and Kentucky and also provides support via the Collaborative Communities Model to HIEs in Bloomington, Indiana and Springfield, Ohio. HealthBridge was recently selected by the Office of the National Coordinator as one of the initial 32 HIT Regional Extension Centers.

    Rodney is also involved in several HIT standards development processes and HealthBridge is one of the 15 organizations in the ONC Nationwide Health Information Network Collaborative (NHIN) effort.
  • Achieving Meaningful Use: Best Practices and Practical Approaches Recorded: Apr 7 2010 41 mins
    Bill Beighe; CIO, Physicians Medical Group of Santa Cruz
    Learn how a community is successfully pursuing health information exchange, interoperability and meaningful use across small and medium practices, hospitals and facilities using a combination of tools, guidance and incentives. This "Roadmap to Meaningful Use" program helps providers realize the quality, efficiency and financial incentives promised in the ARRA Stimulus funding.
  • Insane Ideas in Healthcare IT Recorded: Apr 7 2010 40 mins
    Christine D. Chang; Ovum, Analyst of Healthcare Technology
    All great ideas sound “insane” at first. This presentation will describe three insane ideas that Ovum believes will transform healthcare in the future including:
    • Telehealth is for everyone, not just the elderly.
    • Patient self-diagnosis is good and should be promoted.
    • Personal health records are not just a passing trend, they are the solution.
  • Fraud & Abuse in the EHR Recorded: Oct 23 2009 36 mins
    Jean Bishop, J Bishop Consulting
    Electronic health records may generate a new set of potential healthcare compliance risks and vulnerabilities. The new risk areas, including, the lack of authentication issues, over-documentation and/or cloning, may have significant ramifications beyond billing and coding. Electronic documentation tools offer exciting features designed to enhance communication for most health record users. The use of the system or specific features without appropriate education, training, infrastructure and monitoring may generate data integrity issues, manufactured documentation, increased risk exposure or even undesirable clinical outcomes. This presentation addresses certain areas of concern and discusses potential approaches for detection, evaluation and corrective action.
  • How Great EHRs Empower Participatory Medicine Recorded: Oct 20 2009 47 mins
    e-Patient Dave deBronkart; Society for Participatory Medicine co-chair
    When I tried to move my health data from my hospital to Google Health, what happened was front page news; the transfer was so bad it was covered by the Information Quality Trainwrecks blog. But that doesn't change my conviction one bit: Good quality data, well managed, can vastly empower the new world of doctor-patient collaboration known as Participatory Medicine.

    As an empowered e-patient, a business process analyst and a day-job data geek, in this talk I'll lay out the Society's vision for the role a good EHR can play in creating more efficient - and more effective - healthcare, in ways that benefit providers and patients alike.
  • Introduction to Clinical Groupware Recorded: Oct 20 2009 49 mins
    David C. Kibbe of AAFP &Vince Kuraitis of Better Health Technologies
    Clinical groupware is a new and evolving model for the development and deployment of health information technology (HIT) platforms and applications having the following characteristics:
    Use of the Internet and the web for EHR technology.
    Explicit design for information sharing and online communication among providers and patients/consumers.
    A modular or component architecture upon which applications can be aggregated to meet specific clinical and workflow tasks.
    Patient/consumer engagement tools that facilitate ongoing health management and care coordination.
    Interface and data exchange standards for information sharing that emerge in a market-driven manner.
    The Clinical Groupware Collaborative is in a formative stage organization. To date, representatives from over 50 companies have expressed interest. We are working to be formally incorporated in November 2009.
  • New HIPAA Rules and EHRs: ARRA & Breach Notification Recorded: Oct 20 2009 47 mins
    Raj Goel, Brainlink International; Jim Sheldon-Dean, Lewis Creek Systems
    New HIPAA Rules and EHRs: ARRA & Breach Notification
  • Business Associates Now and Then: HIPAA, EHRs and the HITECH Act Recorded: Oct 20 2009 48 mins
    Susan Miller, Security & Privacy Work Group Chair, WEDI with Jim Sheldon-Dean
    Business Associates first made their appearance in the HIPAA regulations almost a decade ago. During the first few years under the HIPAA regulations business associates used PHI of a HIPAA covered entity to do work for the covered entity including claims processing, data analysis, utilization review, benefit management, and practice management. In other words, the work was in the areas of administration, payment and health care operations. This electronic data sharing was between no more than two or three entities.

    The world has advanced and we now have Electronic Health Records (EHRs), Personal Health Records (PHRs), Regional Health Information Organizations (RHIOs) and Health Information Interchanges (HIEs) that share clinical information electronically. This data sharing is among a much larger universe, among many more entities, through much different technologies.

    Until the HITECH Act PHRs, RHIOs and HIEs were not business associates. Business associates now include these new forms of clinical data repositories and sharing organizations and must keep most of the HIPAA privacy and security requirements as if they are covered entities and not just through a contract, a business associate agreement with a covered entity.

    This session will outline the new world of business associates in clinical information sharing.
  • Kaiser Permanente's Journey and Ultimate Success with Health IT Recorded: Oct 20 2009 46 mins
    Andrew M. Wiesenthal; The Permanente Federation; Associate Executive Director
    There is increasing interest in the United States and abroad in implementing electronic health records as part of an effort to improve the process, cost, and outcomes of health care. Kaiser Permanente has been working toward a goal of automating all health information on its 8.6 million members. Work began, in some ways more than 30 years ago. With focus on a vision for health care in the 21st century, our Kaiser Permanente HealthConnect® electronic health record has been fully deployed in all of our 431 medical offices, and 33 of our 36 hospitals (the remainder will be completed in the first quarter of 2010). We have also deployed a personal health record actively used by more than 3 million members. Along the way to this success, we have made mistakes and learned many hard lessons. The presentation will share that experience and describe some of the benefits of the system.
  • FDA & Internet: Lessons & Scenarios for Biopharma Communicators Recorded: Jul 23 2009 60 mins
    Max Talbott, FDA; Joanna Napp, Jackson Walker; Jeffery Drummond, Jackson Walker
    This panel, moderated by David Maizenberg, will feature former Division Director at FDA and 30 year biopharma veteran, Max Talbott, Joanna Napp, Healthcare and IP partner at Jackson Walker, and health care law expert Jeffery Drummond. The discussion will cover FDA regulation of Internet-based communications by biopharmaceutical companies, starting with the recent keyword advertising warning letters and subsequent draft regulations. The panel will also delve into possible scenarios for biopharmaceutical company participation in conversational and social media: the next frontier for communications with doctors, patients and wider communities of interest.
  • When does Discovery become Patentable Invention? Recorded: Jul 23 2009 44 mins
    John Richards, Ladas & Parry LLP
    The patent system is based on a social contract between the inventor and the state. In return for a disclosure of the invention by the inventor, the state grants the inventor or his assignee a period in which he can exclude others from using his or her invention. The two sides of this contract are reflected in the two principle parts of a patent:1) the description of the invention and how to put it into practice and 2) the claims or definition of the invention which determine who one can sue for trespassing onto one's invention. In recent years the courts have placed increased emphasis on trying to establish a proper balance between the contribution made by the description and the permissible breadth of the definition set out in the claims. Different countries can take different views as to where the balance point should lie. In today's global marketplace, such differences can be very important.

    In this presentation we will look at how pharmaceutical inventions may be defined and the requirements of the disclosure in order to support such definitions with particular emphasis on issues that arise as one moves from an appreciation of the significance of a new biochemical discovery to using that discovery as a basis for treatment. If one files a patent application too early with insufficient disclosure the courts may conclude that one is merely speculating and not entitled to a patent because "the invention" has not yet been made. If one waits too long, noe may lose the race to the patent office. The presentation will try to untangle the issues involved.
  • Open Notebook Science for Collaborative Drug Discovery Recorded: Jul 23 2009 39 mins
    Jean-Claude Bradley, Associate Professor, Drexel University
    Open Notebook Science for Collaborative Drug Discovery
  • Developing Therapeutics: The Path Less Traveled Recorded: Jul 23 2009 45 mins
    John Oyler, CEO, BioDuro
    The current business model for biotech and pharmaceutical companies is broken. Every aspect of R&D has changed over the last 20 years, yet analysis of the industry is still based on oversimplified models. As a result of this global financial crisis, the impact of reduced research budgets of pharmaceutical and biotech companies will be played out for the next 3-5 years. There is a need to develop new therapeutics and appropriate business models that clearly demonstrate the compelling value to invest in, and develop, new therapeutics. Four compelling reasons challenging assumptions on investment and motivations discuss why walking the path less traveled could make all the difference. An opportunity exists; with new business models, collaboration across the industry and hard work, success can be exploited from this situation.
  • Understanding eHealth Sustainability in Developing Countries Recorded: Jul 15 2009 49 mins
    Adesina Iluyemi, Head of Global Health Commission at NEPAD Council
    Understanding eHealth Sustainability in Developing Countries: The Five 'Is' Concept
  • Federal Health Architecture: The CONNECT Solution Recorded: Jul 8 2009 33 mins
    Craig Miller, Federal Health Architecture CONNECT Initiative Chief Architect
    This session will provide attendees with: an update on the CONNECT solution; an overview of how federal agencies are using the solution to tie into the Nationwide Health Information Network; and outline of the benefits that federal participation in the NHIN and will provide to patients, care providers, payers and other health stakeholders. This session will also detail citizen to citizen benefits that a nationwide network of interoperable health IT will provide, ranging from improved healthcare and faster benefits administration to quicker identification and response to public health emergencies.

    Craig Miller

    Miller is the chief architect for CONNECT, a SOA-based solution that connects federal agencies into nationwide health information exchanges. As a strategic advisor to the Federal Health Architecture (FHA) program, he guides the development of CONNECT and other federal solutions based on his expertise in electronic health information exchange, electronic health records and service-oriented architecture. Miller has more than 12 years of enterprise architecture experience at the director level, working with agencies such as HHS, CMS, FDA, USDA and OMB. He was the lead enterprise architect for HHS’ department-wide enterprise architecture initiative, and He led the development of versions 2.0-2.2 of the OMB EA Assessment Framework and was responsible for developing the structure of the Federal Transition Framework.
  • Write an RFP That Delivers ROI Recorded: Jul 8 2009 49 mins
    Ben Dillon, VP, Geonetric
    Too often hospital marketing or IT departments send off requests for proposals (RFPs) that list wanted functionally, and then wonder why their Web site vendor doesn't provide strategic value. The fact is, if you outsource some or part of your online initiatives, it's more important than ever that your vendor is proving their value. Join Geonetric as we help you look at your relationship with vendors in a strategic way, from RFP creation to ensuring continuous return on investment.

    Please attend this Webinar if you want to learn more about:
    - How to implement an effective process for selecting a Web partner
    - What to include in an RFP to attract the right Web partners
    - How to define Web goals and align them with what your Web partner is delivering
    - How to develop long-term strategies with your vendor
  • The Future of Disease & Care Management for the Chronically Ill Recorded: Jul 8 2009 46 mins
    Jaan Sidorov, The Disease Care Management Blog
    The Future of Disease & Care Management for the Chronically Ill
Healthcare Trends and Solutions
This channel will feature presentations by influential representatives from academia, producers, healthcare providers, payers and regulators to explore hot topics in healthcare. Thought leaders will debate the scientific, economical and political challenges and propose viable solutions to optimizing healthcare and medicine.

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  • Title: Delaying the onset of aging via rejuvenated stem cell responses
  • Live at: May 12 2009 5:00 pm
  • Presented by: Professor Irina Conboy, PhD Department of Bioengineering, UC Berkeley
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