The model of biomedical research-by-consortium has gained traction internationally. But many are faced with challenges on demonstrating the value that they provide to their various stakeholders. This presentation was made at the 2014 Science of Team Science conference and more open-access material can be found at a recent Science Translational Medicine article http://bit.ly/STMConsortia
This presentation was made at a large pharmaceutical company's R&D and corporate affairs campus - going a little more indepth than the one from the prior Science of Team Science Conference
Investigator-initiated clinical trials: a community perspectiveARDC
Presentation by Miranda Cumpston, ACTA, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Multi-Stakeholder Dialogues Addressing Needs, HTA Requirements and Good Pract...Office of Health Economics
Despite social, political and economic differences in emerging countries, health systems are characterized by certain common challenges and needs. HTA has been recognize by WHO as a tool to facilitate Universal Health Coverage and Reimbursement decisions and HTAi society have been promoting multi stakeholder dialogues. What impact and actions have emerged from the discussions held to date? This presentation includes Adrian Towse's slides from a panel session that included other contributors.
Author(s) and affiliation(s): Adrian Towse, Office of Health Economics
Conference/meeting: Health Technology Assessment International (HTAi) 2018
Location: Vancouver, Canada
Date: 04/06/2018
Adrian Towse's slides from a session will exploring how the benefits of antibiotics can best be captured in HTA, and how we should pay for them when their value may depend on restricting their use.
Author(s) and affiliation(s): Adrian Towse, Office of Health Economics
Conference/meeting: Health Technology Assessment International (HTAi) 2018
Location: Vancouver, Canada
Date: 03/06/2018
More than an umbrella term, open science is moving towards broadening and integrating the open access movement to scholarly literature on other fronts, such as open scientific data, open scientific tools, open notebook science, open education, and citizen science.
This “movement of movements” transforms the scenario and the dynamics of science collaboration, communication and dissemination, expanding its ability to respond to contemporary new and complex issues, while posing new challenges. On the one hand, new possibilities arise for the generation of social, economic and environmental benefits, as well as innovation, associated to increased reach, speed and quality of production and circulation of scientific knowledge, its results and possible uses. On the other hand, new institutional and technological requirements are imposed on the adoption of open research policies, strategies, and practices (regulations, capacities, infrastructures, and tools), and the costs derived therefrom. A new economics of open science is being developed, together with new business models, with repercussions on the present and future of scientific journals and their relationship with other scientific publication and publicization systems emerging from this framework, as well as with the monitoring, evaluation and research financing apparatuses.
At the same time, it is about facing the challenge of bridging the gap between science (and its various forms of data availability) and policy. Today there is an abyss in this interface that should be narrowing so that, increasingly, political decisions, particularly those that affect social and environmental issues more directly are based on quality and plural science. To strengthen this relationship, efforts are needed to reconcile languages and times that allow virtuous dialogue between these two fields.
In the end, it is also important to recognize the different implications of this changing scenario regarding more and less developed countries, placing new opportunities and barriers for their science, technology and innovation systems and their respective repositioning in the global scenario.
Syllabus
Open science, science communication and the challenges of sustainable development; open publications and innovation; the new economy (politics) of open science and its infrastructures of scholarly communication: costs and benefits (academic, social, and economic); political and institutional requirements; business models emerging from open scientific publications; opportunities and challenges for developing countries.
This presentation was provided by Holly Falk-Krzesinski of Elsevier during the NISO event, "Is This Still Working? Incentives to Publish, Metrics, and New Reward Systems," held on February 20, 2019.
This presentation was made at a large pharmaceutical company's R&D and corporate affairs campus - going a little more indepth than the one from the prior Science of Team Science Conference
Investigator-initiated clinical trials: a community perspectiveARDC
Presentation by Miranda Cumpston, ACTA, to the 'Unlocking value from publicly funded Clinical Research Data' workshop, cohosted by ARDC and CSIRO at ANU on 6 March 2019.
Multi-Stakeholder Dialogues Addressing Needs, HTA Requirements and Good Pract...Office of Health Economics
Despite social, political and economic differences in emerging countries, health systems are characterized by certain common challenges and needs. HTA has been recognize by WHO as a tool to facilitate Universal Health Coverage and Reimbursement decisions and HTAi society have been promoting multi stakeholder dialogues. What impact and actions have emerged from the discussions held to date? This presentation includes Adrian Towse's slides from a panel session that included other contributors.
Author(s) and affiliation(s): Adrian Towse, Office of Health Economics
Conference/meeting: Health Technology Assessment International (HTAi) 2018
Location: Vancouver, Canada
Date: 04/06/2018
Adrian Towse's slides from a session will exploring how the benefits of antibiotics can best be captured in HTA, and how we should pay for them when their value may depend on restricting their use.
Author(s) and affiliation(s): Adrian Towse, Office of Health Economics
Conference/meeting: Health Technology Assessment International (HTAi) 2018
Location: Vancouver, Canada
Date: 03/06/2018
More than an umbrella term, open science is moving towards broadening and integrating the open access movement to scholarly literature on other fronts, such as open scientific data, open scientific tools, open notebook science, open education, and citizen science.
This “movement of movements” transforms the scenario and the dynamics of science collaboration, communication and dissemination, expanding its ability to respond to contemporary new and complex issues, while posing new challenges. On the one hand, new possibilities arise for the generation of social, economic and environmental benefits, as well as innovation, associated to increased reach, speed and quality of production and circulation of scientific knowledge, its results and possible uses. On the other hand, new institutional and technological requirements are imposed on the adoption of open research policies, strategies, and practices (regulations, capacities, infrastructures, and tools), and the costs derived therefrom. A new economics of open science is being developed, together with new business models, with repercussions on the present and future of scientific journals and their relationship with other scientific publication and publicization systems emerging from this framework, as well as with the monitoring, evaluation and research financing apparatuses.
At the same time, it is about facing the challenge of bridging the gap between science (and its various forms of data availability) and policy. Today there is an abyss in this interface that should be narrowing so that, increasingly, political decisions, particularly those that affect social and environmental issues more directly are based on quality and plural science. To strengthen this relationship, efforts are needed to reconcile languages and times that allow virtuous dialogue between these two fields.
In the end, it is also important to recognize the different implications of this changing scenario regarding more and less developed countries, placing new opportunities and barriers for their science, technology and innovation systems and their respective repositioning in the global scenario.
Syllabus
Open science, science communication and the challenges of sustainable development; open publications and innovation; the new economy (politics) of open science and its infrastructures of scholarly communication: costs and benefits (academic, social, and economic); political and institutional requirements; business models emerging from open scientific publications; opportunities and challenges for developing countries.
This presentation was provided by Holly Falk-Krzesinski of Elsevier during the NISO event, "Is This Still Working? Incentives to Publish, Metrics, and New Reward Systems," held on February 20, 2019.
Real World Evidence - getting value from volume with metadataAnn Kelly
Anne Lapkin from Smartlogic and Bill Fox from MarkLogic webinar on Real World Evidence; the value, the opportunity, the problems and the platform of the future
25 January 2022: Webinar on Adverse Outcome Pathway co-operative activities b...OECD Environment
On 25 January 2022, the OECD held a webinar on Adverse Outcome Pathway (AOP) co-operative activities between Scientific journals and the OECD.
This webinar was organised primarily for Scientific Journal editors or publishers who are interested in reviewing/publishing AOPs and collaborating with the OECD in this activity.
The objective of the webinar was to present the basis for cooperation between scientific journals and the OECD and discuss the lessons learnt so far.
Dan Villeneuve (US EPA) presented the AOP framework and challenges being encountered.
Access the webinar replay at: https://oe.cd/testing-assessment-webinars
The Green Park Collaborative (GPC) has developed a new tool to help health care decision makers confidently and consistently use Real World Evidence (RWE) when making tough coverage and care choices. Called RWE Decoder, the spreadsheet-based assessment tool lets users review and evaluate all existing studies and evidence for both rigor and relevance. Informed by these factors, users can assess study quality, and generate a visual summary to help gauge the evidence under review.
Published RWE studies developed from data-rich electronic medical records or medical claims data are increasingly available from health care systems. However, the quality of this research can vary widely, and payers, clinicians and other health care decision makers often dismiss it out of hand. RWE Decoder and its associated user guide and framework, offer a thoughtful approach to helping these decision makers assess whether RWE studies address their questions and can appropriately guide their choices.
The tool, user guide, and supporting white paper are available here: https://goo.gl/AhbHUw
Clinical Trial Data Transparency: Explaining Governance for Public Data SharingHealth Data Consortium
Watch the webinar here: http://www.screencast.com/t/0lATKYlJ8
Dr. Chris Boone, then-VP in Avalere’s Evidence Translation and Implementation Practice, discussed clinical trial data transparency and considerations for governance and open data sharing. Clinical trials are extremely valuable as the primary data source for seeking regulatory approval of products. Historically, regulatory agencie have been the sole recipients of clinical trial data, butthere has been a recent push from various stakeholder groups to open access to clinical trial data to non-regulatory researchers as an act of ethical responsibility to patients, a contribution to public health, and a demonstrated commitment to advancing the science. Some of the barriers include developing a sound approach for de-identifying patient data, adopting universal clinical trial data format, and managing the proactive and non-selective access and security of clinical data once collected. Dr. Boone discusses rationales and benefits/risks of clinical trial transparency, responsible use of publicly sharing this data, barriers and legal implications, and reasonable data sharing models.
Discover more health data resources on our website at http://www.healthdataconsortium.org/
ImpactSense Research Bootcamp - Maximising Your Research Practices for 2020 a...Veronica Massoud
We hosted a Bootcamp on real-world research practices and applicable strategies to implement into your business. It's a is a unique opportunity to explore decades of gathered insight from CX professionals - looking at everything from quant and qual techniques to using machine learning to filter through data.
The issue of open-source models in the cost-effectiveness and disease-level (collaborative) models has been brewing for many years. There has been a marked growth in open science, and funding bodies and publishers increasingly require that research data be made available. As mentioned in our previous Issue Panel, “cost-effectiveness models synthesise a wide range of evidence to facilitate extrapolation over time and from intermediate to final decision endpoints. These models are often statistically sophisticated and require assumptions that are not directly testable. This can lead to decision-makers “discounting” the results of cost-effectiveness analyses, particularly if the developer is seen as partial.” Open-source models, then, would encourage greater transparency in pharmacoeconomic modeling and the reuse and updating of the best/most useful models; they are essential if cost-effectiveness analyses are to be widely accepted to reduce bias, increase transparency, improve model access, and allow for faster access to critical knowledge. The ISPOR-SMDM guidelines and the EUnetHTA joint action projects, are supportive of these views on collaboration, transparency, confidentiality, processes and consistency offered by the availability of open-source models to improve decision-making around health care and reimbursement. With openness and sharing, however, come issues of copyright and access and a need to define how model sharing can be achieved in a fair and equitable manner. There is, therefore, a need to develop an ongoing dialog on openness, especially where the research may be considered precompetitive and not worthy of IP investment. The pros and cons of open source models and the proposed mission of the Open Source Model SIG to curate an ongoing dialog regarding issues around creating, disseminating, sharing, evaluating, and updating open source cost-effectiveness and comparative effectiveness models will be debated amongst SIG members.
Author(s) and affiliation(s): Nancy Risebrough, Senior Principal, ICON plc, Toronto, Canada Jeroen P Jansen; Innovation & Value Initiative; Precision Medicine Group; and Stanford University Lotte Steuten, Vice President & Head of Consulting, Office of Health Economics, UK Renée JG Arnold, PharmD, RPh, ICON plc, New York, NY and Icahn School of Medicine at Mount Sinai, New York, NY, USA
Event: ISPOR 2019 Annual Meeting
Date: 20/05/2019
Consortium metrics discussion with IOM Drug ForumMark David Lim
Presentation made to the IOM Forum on Drug Discovery, Development, and Translation to explore the possibility of metrics that evaluate the performance of biomedical research consortia
Real World Evidence - getting value from volume with metadataAnn Kelly
Anne Lapkin from Smartlogic and Bill Fox from MarkLogic webinar on Real World Evidence; the value, the opportunity, the problems and the platform of the future
25 January 2022: Webinar on Adverse Outcome Pathway co-operative activities b...OECD Environment
On 25 January 2022, the OECD held a webinar on Adverse Outcome Pathway (AOP) co-operative activities between Scientific journals and the OECD.
This webinar was organised primarily for Scientific Journal editors or publishers who are interested in reviewing/publishing AOPs and collaborating with the OECD in this activity.
The objective of the webinar was to present the basis for cooperation between scientific journals and the OECD and discuss the lessons learnt so far.
Dan Villeneuve (US EPA) presented the AOP framework and challenges being encountered.
Access the webinar replay at: https://oe.cd/testing-assessment-webinars
The Green Park Collaborative (GPC) has developed a new tool to help health care decision makers confidently and consistently use Real World Evidence (RWE) when making tough coverage and care choices. Called RWE Decoder, the spreadsheet-based assessment tool lets users review and evaluate all existing studies and evidence for both rigor and relevance. Informed by these factors, users can assess study quality, and generate a visual summary to help gauge the evidence under review.
Published RWE studies developed from data-rich electronic medical records or medical claims data are increasingly available from health care systems. However, the quality of this research can vary widely, and payers, clinicians and other health care decision makers often dismiss it out of hand. RWE Decoder and its associated user guide and framework, offer a thoughtful approach to helping these decision makers assess whether RWE studies address their questions and can appropriately guide their choices.
The tool, user guide, and supporting white paper are available here: https://goo.gl/AhbHUw
Clinical Trial Data Transparency: Explaining Governance for Public Data SharingHealth Data Consortium
Watch the webinar here: http://www.screencast.com/t/0lATKYlJ8
Dr. Chris Boone, then-VP in Avalere’s Evidence Translation and Implementation Practice, discussed clinical trial data transparency and considerations for governance and open data sharing. Clinical trials are extremely valuable as the primary data source for seeking regulatory approval of products. Historically, regulatory agencie have been the sole recipients of clinical trial data, butthere has been a recent push from various stakeholder groups to open access to clinical trial data to non-regulatory researchers as an act of ethical responsibility to patients, a contribution to public health, and a demonstrated commitment to advancing the science. Some of the barriers include developing a sound approach for de-identifying patient data, adopting universal clinical trial data format, and managing the proactive and non-selective access and security of clinical data once collected. Dr. Boone discusses rationales and benefits/risks of clinical trial transparency, responsible use of publicly sharing this data, barriers and legal implications, and reasonable data sharing models.
Discover more health data resources on our website at http://www.healthdataconsortium.org/
ImpactSense Research Bootcamp - Maximising Your Research Practices for 2020 a...Veronica Massoud
We hosted a Bootcamp on real-world research practices and applicable strategies to implement into your business. It's a is a unique opportunity to explore decades of gathered insight from CX professionals - looking at everything from quant and qual techniques to using machine learning to filter through data.
The issue of open-source models in the cost-effectiveness and disease-level (collaborative) models has been brewing for many years. There has been a marked growth in open science, and funding bodies and publishers increasingly require that research data be made available. As mentioned in our previous Issue Panel, “cost-effectiveness models synthesise a wide range of evidence to facilitate extrapolation over time and from intermediate to final decision endpoints. These models are often statistically sophisticated and require assumptions that are not directly testable. This can lead to decision-makers “discounting” the results of cost-effectiveness analyses, particularly if the developer is seen as partial.” Open-source models, then, would encourage greater transparency in pharmacoeconomic modeling and the reuse and updating of the best/most useful models; they are essential if cost-effectiveness analyses are to be widely accepted to reduce bias, increase transparency, improve model access, and allow for faster access to critical knowledge. The ISPOR-SMDM guidelines and the EUnetHTA joint action projects, are supportive of these views on collaboration, transparency, confidentiality, processes and consistency offered by the availability of open-source models to improve decision-making around health care and reimbursement. With openness and sharing, however, come issues of copyright and access and a need to define how model sharing can be achieved in a fair and equitable manner. There is, therefore, a need to develop an ongoing dialog on openness, especially where the research may be considered precompetitive and not worthy of IP investment. The pros and cons of open source models and the proposed mission of the Open Source Model SIG to curate an ongoing dialog regarding issues around creating, disseminating, sharing, evaluating, and updating open source cost-effectiveness and comparative effectiveness models will be debated amongst SIG members.
Author(s) and affiliation(s): Nancy Risebrough, Senior Principal, ICON plc, Toronto, Canada Jeroen P Jansen; Innovation & Value Initiative; Precision Medicine Group; and Stanford University Lotte Steuten, Vice President & Head of Consulting, Office of Health Economics, UK Renée JG Arnold, PharmD, RPh, ICON plc, New York, NY and Icahn School of Medicine at Mount Sinai, New York, NY, USA
Event: ISPOR 2019 Annual Meeting
Date: 20/05/2019
Consortium metrics discussion with IOM Drug ForumMark David Lim
Presentation made to the IOM Forum on Drug Discovery, Development, and Translation to explore the possibility of metrics that evaluate the performance of biomedical research consortia
mHealth and Wireless Technology Conference Partnering with academic organizat...P. Kenyon Crowley
How companies can partner with research organizations to accelerate research and development, evaluation of products, enhance usability, and create value. Includes funding relevant to mobile health companies.
Gather evidence to demonstrate the impact of your researchIUPUI
This workshop is the 3rd in a series of 4 titled "Maximize your impact" offered by the IUPUI University Library Center for Digital Scholarship. Faculty must provide strong evidence of impact in order to achieve promotion and tenure. Having strong evidence in year 5 is made easier by strategic dissemination early in your tenure track. In this hands-on workshop, we will introduce key sources of evidence to support your case, demonstrate strategies for gathering this evidence, and provide a variety of examples. These sources include citation metrics, article level metrics, and altmetrics as indicators of impact to support your narrative of excellence.
EcoZD research units: Bridges and barriers to integrative research approachesILRI
Presented by Rainer Asse to the Progress Meeting on Ecosystem Approaches to the Better Management of Zoonotic Emerging Infectious Diseases in the South East Asian Region, Bangkok, 10-13 December 2011.
LITA’s Altmetrics and Digital Analytics Interest Group is proud to present Heather Coates, Richard Naples, and Lauren Collister in our second free webinar of the season. Heather will introduce the concept of altmetrics with a quick "Altmetrics 101," Richard will discuss the Smithsonian's implementation of Altmetric, and Lauren will share the University of Pittsburgh's experience with Plum Analytics.
The NIHR Research Design Service provides support to NHS staff and academics preparing research proposals for submission to peer-reviewed funding competitions for applied health or social care research.
We describe what we have learned from four years of collaborating across the industry/not-for-profit boundary. Over this time we pursued multiple projects and some of the lessons learned are described here.
Many large pharma companies have reduced their research activity at the very early, hit- and lead- seeking phase of research. To compensate, organisations are becoming more porous and working more collaboratively in risk-sharing arrangements. Both parties need to give up some control, but gain a great deal in return
Shift Health co-hosted a Product Development Boot Camp with the Global HIV Vaccine Enterprise. The Boot Camp afforded workshop participants an opportunity to discuss best practices, to learn from the experience of other experts and to create an enduring resource and toolkit that will serve the HIV vaccine field and beyond.
Product development refers to the multifaceted, long-term, highly regulated process that brings promising new drugs, vaccines and medical devices to the populations who most need them. In fields such as HIV vaccine development, where the absence of commercial incentives can make it difficult for companies to lead this process on their own, inventors need to work in partnership with diverse stakeholders and funders to maximize the social and economic impact of their research.
Ryan Wiley, PhD, President at Shift Health, delivered an overview of product development partnerships, which exhibit three common elements:
Defined governance mechanisms that enable appropriate participation in decision-making
Disciplined approach to communication among partners and with stakeholders
IP policies that balance the needs of individual partners with the objectives of the partnership.
Senior Project and Engineering Leader Jim Smith.pdfJim Smith
I am a Project and Engineering Leader with extensive experience as a Business Operations Leader, Technical Project Manager, Engineering Manager and Operations Experience for Domestic and International companies such as Electrolux, Carrier, and Deutz. I have developed new products using Stage Gate development/MS Project/JIRA, for the pro-duction of Medical Equipment, Large Commercial Refrigeration Systems, Appliances, HVAC, and Diesel engines.
My experience includes:
Managed customized engineered refrigeration system projects with high voltage power panels from quote to ship, coordinating actions between electrical engineering, mechanical design and application engineering, purchasing, production, test, quality assurance and field installation. Managed projects $25k to $1M per project; 4-8 per month. (Hussmann refrigeration)
Successfully developed the $15-20M yearly corporate capital strategy for manufacturing, with the Executive Team and key stakeholders. Created project scope and specifications, business case, ROI, managed project plans with key personnel for nine consumer product manufacturing and distribution sites; to support the company’s strategic sales plan.
Over 15 years of experience managing and developing cost improvement projects with key Stakeholders, site Manufacturing Engineers, Mechanical Engineers, Maintenance, and facility support personnel to optimize pro-duction operations, safety, EHS, and new product development. (BioLab, Deutz, Caire)
Experience working as a Technical Manager developing new products with chemical engineers and packaging engineers to enhance and reduce the cost of retail products. I have led the activities of multiple engineering groups with diverse backgrounds.
Great experience managing the product development of products which utilize complex electrical controls, high voltage power panels, product testing, and commissioning.
Created project scope, business case, ROI for multiple capital projects to support electrotechnical assembly and CPG goods. Identified project cost, risk, success criteria, and performed equipment qualifications. (Carrier, Electrolux, Biolab, Price, Hussmann)
Created detailed projects plans using MS Project, Gant charts in excel, and updated new product development in Jira for stakeholders and project team members including critical path.
Great knowledge of ISO9001, NFPA, OSHA regulations.
User level knowledge of MRP/SAP, MS Project, Powerpoint, Visio, Mastercontrol, JIRA, Power BI and Tableau.
I appreciate your consideration, and look forward to discussing this role with you, and how I can lead your company’s growth and profitability. I can be contacted via LinkedIn via phone or E Mail.
Jim Smith
678-993-7195
jimsmith30024@gmail.com
Oprah Winfrey: A Leader in Media, Philanthropy, and Empowerment | CIO Women M...CIOWomenMagazine
This person is none other than Oprah Winfrey, a highly influential figure whose impact extends beyond television. This article will delve into the remarkable life and lasting legacy of Oprah. Her story serves as a reminder of the importance of perseverance, compassion, and firm determination.
Artificial intelligence (AI) offers new opportunities to radically reinvent the way we do business. This study explores how CEOs and top decision makers around the world are responding to the transformative potential of AI.
The Team Member and Guest Experience - Lead and Take Care of your restaurant team. They are the people closest to and delivering Hospitality to your paying Guests!
Make the call, and we can assist you.
408-784-7371
Foodservice Consulting + Design
The case study discusses the potential of drone delivery and the challenges that need to be addressed before it becomes widespread.
Key takeaways:
Drone delivery is in its early stages: Amazon's trial in the UK demonstrates the potential for faster deliveries, but it's still limited by regulations and technology.
Regulations are a major hurdle: Safety concerns around drone collisions with airplanes and people have led to restrictions on flight height and location.
Other challenges exist: Who will use drone delivery the most? Is it cost-effective compared to traditional delivery trucks?
Discussion questions:
Managerial challenges: Integrating drones requires planning for new infrastructure, training staff, and navigating regulations. There are also marketing and recruitment considerations specific to this technology.
External forces vary by country: Regulations, consumer acceptance, and infrastructure all differ between countries.
Demographics matter: Younger generations might be more receptive to drone delivery, while older populations might have concerns.
Stakeholders for Amazon: Customers, regulators, aviation authorities, and competitors are all stakeholders. Regulators likely hold the greatest influence as they determine the feasibility of drone delivery.
5. Sci. Trans. Medicine, June 2014
http://bit.ly/STMConsortia
Operational Framework Landscape
consortiapedia.fastercures.org
• Mission/governance
• Financing
• Data-sharing
• Intellectual property
• and others…
Database
369 consortia
• Disease focus
• Types of tools
• Where and who
• Why
Planned release:
end of 2014
• Consortium-provided
content
• Cross-comparison of
consortia
• Point-of-contact
6. Who and what
Sci. Trans. Medicine, June 2014
http://bit.ly/STMConsortia
7. More than half focused on disease/condition
Sci. Trans. Medicine, June 2014
http://bit.ly/STMConsortia
Sharing comparator arm
data from clinical trials
Research assays,
animal models
Genomic/clinical
databaseT2D patients
AgedBrainSYSBIO
Age-associated
pathways
9. Consortium lifespan: 5 - 6 years
Inception
Ramp up
Mid-stream
Wind down
Closure
| 1 year | 2 - 3 years | 1 year |
Scientific challenge
Sponsor engagement
Governance
Agreements
Tool concept
Engaging tool-builders
Project plan
Project launch
Team culture
Infrastructure
Project execution
Milestones Deliverables
Licensing/IP
Dissemination Data management
Licensing/IP
Dissemination
Royalties
10. Evaluation = Support
Inception
Ramp up
Mid-stream
Wind down
Closure
| 1 year | 2 - 3 years | 1 year |
Financial and in-kind commitment
Monitoring & Evaluation
Steering
Committee
Board of
Directors
11. Complex virtual relationships
Board of directors
Steering
committee
Oversight
Management
President /
Executive director
Project manager
Project Team
Project manager Scientific team
14. Whose value-add?
Government • public health
• regulatory science
• de-risk innovation
• economic growth
Industry • accelerate pipeline
• new therapeutic area
• access resources
• de-risk innovation
• access intellectual
capital
Academia • access resources
• opportunities for
publications
• training opportunities
• identify collaborators
Patient
organizations
• accelerate pipelines
• advance basic
research
• de-risk medical
product development
Consortium
researchers
• simplify day jobs
• access resources
• networking
• training / education
15. Bibliometrics
is this all we can measure?
• By the end of 2013, IMI projects had
delivered over 600 scientific
publications in over 300 journals
• The citation index of papers from IMI
projects is twice the world average,
and higher than the EU average.
.
Data & analysis: Thomson Reuters (Custom Analytics & Engineered Solutions), 2013
16. Bibliometrics and collaboration
Pre IMI funding award Post IMI funding award
Data & analysis: Thomson Reuters (Custom Analytics & Engineered Solutions), 2013
17. Collaborations – who / what
Co-authorship – 69%
Cross-sector collaboration – 42%
Cross-project collaboration – 37%
Cross-disease collaboration – 31%
IMI researcher networks by sector
Data & analysis: Thomson Reuters (Custom Analytics & Engineered Solutions), 2013
18. Not all consortium outputs are “publishable” – licenses, databases
Publications are retrospective, often-times at completion of project
Virtual collaborations - no dedicated laboratory/workspace
Bias: "Sexiness" of the science
Different stakeholders = different expectations
Semi-committed teams - not their day jobs
Human capital - turnover, advancement
Numerous consortia, different operational models
- cross comparison?
Complexities for evaluation
#
19. Consortium landscape
Hub-and-spoke model – central management, source of info
Innovative Medicines Initiative, Critical Path Initiative,
Foundation for the National Institutes of Health, etc
Annual reports, bibliometric analysis,
Projects that result in change in policy (guildelines)
Press releases
Twitter, Facebook, Youtube, LinkedIn
20. Defining metrics for value-add
Mid-stream analysis: Consortium on-track for deliverables?
- metrics: efficiency, project management, effective collaboration model
- indirect benefits: access resource/expertise
- users: stakeholders, consortium managers
- impact: financing, engagement of participants, additional support
Constraints:
- minimize bias
- scientific goals
- size/financing
- industry as first stakeholder
- generalizable to multiple "similar" consortia
Implementation:
- scope (pre-clinical vs. clinical, by type of output)
- metrics to evaluation
- cross-consortia measurements?