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      THURSDAY 5 JUNE, 2025

      SCIENCE MUSEUM, LONDON

      Prix Galien UK Forum
      Program

      PG_LOGO_edited_Grey-1

      2024 Program


      Mike Rosenblatt
      OPENING REMARKS
      Mike Rosenblatt

      7:40 AM - 7:45 AM

      GALIEN FORUM CO-ChairS

      Michael Rosenblatt
      Galien Forum Co-Chair; Prix Galien Committee Chair (Categories: Pharma, Biotech, Rare/Orphan); Advisory Partner, Ascenta Capital; Senior Advisor to Bain Capital Life Sciences and Flagship Pioneering

       

      Phillip A. Sharp
      Nobel Laureate; Galien Forum Co-Chair; Institute Professor and Professor of Biology Emeritus, Koch Institute for Integrative Cancer Research, MIT

       

      Womens_Health
      PANEL 1
      Womens_Health

      7:45 AM - 9:00 AM

      Women’s Health / Generational Health

      Chair

      Julie Louise Gerberding
      President and Chief Executive Officer, Foundation for the National Institutes of Health

      PANELISTS
      Diana W. Bianchi
      Director, Eunice Kennedy Shriver, National Institute of Child Health and Human Development, NIH
       
      Mary-Ann Etiebet
      President and Chief Executive Officer, Vital Strategies
       
      Elizabeth I. O. Garner
      Former Chief Scientific Officer, Ferring US; Immediate Past President, American Medical Women’s Association

      Sandra Milligan
      President, Aspira Women's Health, Organon

      Sans Thakur
      Founder and Chairwoman of TOWER Capital Group and the pioneer of Generational Health 

      Background and Topics for Discussion:

       

      Decades of institutional neglect and cultural indifference have left a glaring gap in the breadth of knowledge and data on the health of women as compared to men. Improving women’s health is, at its core, an issue of health equity and inclusivity, and would raise the quality of life for women. Such advances would also benefit the global economy and the health of future generations. The McKinsey Health Institute recently published a comprehensive analysis of the impact that a greater investment in women’s health would have on the global economy, along with addressing a significant societal moral benefit. Specifically, an investment to improve women’s health would provide a $1 trillion benefit to the global economy by 2040.

       

      Evidence suggests the value contributions added by women at home, at work, and in the neighborhood increases when their disease burden decreases. A lower incidence of the many health challenges facing women before, during, and beyond their reproductive years could have multiple beneficial effects, including raising economic growth and social resiliency.

       

      As the science behind regenerative medicine improves, gender-specific innovations allow more women to live longer, healthier lives and promise to leave a better genetic footprint for future generations. Such contributions are only now being acknowledged, prioritizing women’s health around a holistic, cross-disciplinary construct called “generational health.” The aim is to emphasize identifying and treating the gender-specific needs of women throughout their life span, beyond their reproductive years.

       

      Prioritizing women’s health remains a work in progress. The good news is many initiatives are being launched to redress the imbalance in women’s health, not only in the levels of public research funding but also in developing new technologies and tools, such as large datasets to allow evaluation of sex and gender differences to treatment response for various diseases. Yet other institutional barriers remain, such as the biopharma industry’s struggle to find a sustainable, long-term commercial business model centered on women’s health. Addressing ingrained, gender-driven resource inequities and recognizing the impact that a greater investment in women’s health would have on the global economy and society is a step forward.

       

      Topics the panel will address include:

       

      • Investment gaps in women’s health: What is the relationship between the prioritization of the social drivers of women’s health and what health systems actually invest in? What is being done to address the scarcity of data on women’s health that perpetuates gender bias and prolongs the underfunding of gender-specific research? Where are we still falling short?
      • Addressing “full spectrum” of women’s health needs: Women’s health traditionally has focused on reproductive health. Has this emphasis led to a neglect of the full spectrum of women’s health needs? Can better health outcomes for women worldwide be secured without an accompanying transformation of the “gender gap” between men and women? Is changing the cultural and socio-economic status of women a public health challenge?
      • Reset of business model to solely focus on women’s health: Are life sciences companies and venture capital funders more –or less– engaged in women’s health now that a reset of the biopharma business model is underway after the pandemic? Is it possible to build a profitable, stand-alone business focused on women’s health?
      Global_Warming_Air_Pollution
      PANEL 2A
      Global_Warming_Air_Pollution

      9:05 AM - 10:05 AM

      Climate Change & Health

      Opening Remarks & Chair

      Rohit Aggarwala
      Chief Climate Officer, City of New York

      PANELISTS
      John Balbus
      Deputy Assistant Secretary for Climate Change and Health Equity and Director, Office of Climate Change and Health Equity, U.S. Department of Health and Human Services
       
      Awa Marie Coll-Seck
      Chair of the Galien Africa; Former Senior Minister to the President of the Republic of Senegal; Former Minister of Health, Republic of Senegal

      Ruxandra Draghia-Akli
      Executive Leader in Life Sciences Innovation and Global Health; Chair of the Scientific Advisory Board, INTREPID Alliance 
       
      Jodi Sherman
      Co-Chair, Lancet Commission on Sustainable Healthcare, Yale
      Panel Background:

      Climate change is disrupting the contours of human health in ways that are only now being assessed and quantified. The markers of mortality and morbidity are legion, from heat-related illnesses that contribute to edema and cardiovascular failure; respiratory ailments like asthma and allergies from airborne pollutants; fatalities, injuries, mental illness and habitat loss from severe weather events; changes in vector ecology that spread malaria, dengue fever and  a host of other pathogens while enhancing prospects for zoonotic disease transmission; water quality impacts, led by cholera; and increased malnutrition induced by climate pressures on the natural environment, farming and the food supply.

      In May, the World Health Assembly (WHO) reiterated its position on climate change as humanity’s single biggest health threat, forecasting 250,000 additional deaths per year worldwide between 2030 and 2050.  The WHO estimates that direct damages to health system infrastructure from extreme weather events alone will total $4bn annually by 2030, a trend destinated to waylay the organization’s plans to introduce a basic global platform of universal health coverage, including access to affordable essential medicines for all, the same year. 

      Vulnerable populations like the poor, children and the elderly will be disproportionately affected. Beyond the documented income losses, climate change undermines many of the basic social determinants of health, such as equality and access to care as well as the local community support structures that act as a hedge against economic displacement and mass migration.

      Pressure is mounting on business and the private-sector to do more to address climate change.  The Intergovernmental Panel on Climate Change (IPCC) has resolved that, to avert a truly catastrophic trajectory to unsustainable weather patterns, action must be taken now to limit carbon emissions and prevent further rises in global temperature by no more than 1.5 C by 2050. Accomplishing this goal depends heavily on the private-sector to help finance a global “green transition” tied to major new investments in renewable, zero-carbon energy technologies that don’t rely on fossil fuels. The IPCC now estimates $2.4 trillion a year in combined global and country financing/investment commitments will be needed well into the next decade to jump start the transition.   

      There is also an expectation that at least a part of this investment be earmarked for countries of the global south, with the preferred vehicle being public-private partnerships involving key multilateral lenders like the World Bank. The idea is to leverage such partnering as a way to “de-risk” the exposure for companies investing in geographies where business confidence is low.

      The health impacts of climate change pose particular challenges for the pharma and biotech sector.    The extensive global supply chains that big pharma companies rely on in the manufacture and distribution of medicines have led to scrutiny by climate change advocates, who are demanding a higher level of “resource stewardship” from management. There is also pressure on the shareholder front to ramp up environmental disclosures and compliance under voluntary company ESG commitments.

      More important, government regulators like the US Securities and Exchange Commission (SEC) and the European Commission are moving forward with plans for even more transparency on industry actions to address climate change.  The SEC rule mandates public companies to report annually on carbon emissions levels, exposure to risks from global warming and the status of strategies to address it.  The EU rule is more prescriptive and calls for evidence on how the company business model and commercial strategies are compatible with the climate reduction provisions of the 2015 Paris Agreement of the UN Framework Convention on Climate Change, including impacts on atmospheric pollution; water and marine resources; and land-based biodiversity and ecosystems – at every step of the company value chain.   

      Overall, climate change makes for more uncertainty for big pharma in operating an essential complex business with numerous customer touchpoints, at scale and across diverse geographies. Extreme weather conditions alone promise supply bottlenecks and product shortages from the loss of manufacturing capacity around temperature-sensitive products with limited shelf life. Long term, the industry will have to confront external demands for changes in its R&D portfolio, in some cases for conditions accentuated by climate change that carry a lower profitability ratio than other disease areas.  Finally, coping with these climate-related risks will require significant new investments in due diligence and hazard avoidance capabilities, extending deep into the third-party supply and support networks where compliance has always been hard to establish. 

      Topics for Discussion:

      • Current state of academic and institutional research on the relationships between climate change and human health – what does the evidence show? Real world implications for health status, public health provision and disease spread if countries fail to meet UN Paris Convention commitments to limit growth in fossil fuel emissions by 2050.
      • Scientific researchers have found a way for plant seeds to effectively fertilize themselves, a discovery with the potential to reduce reliance on fossil fuel-based fertilizers in agriculture. Are there similar impactful innovations underway to address the harmful effects of climate change on disease and other key public health parameters?
      • In the US, just under 10% of our national carbon footprint can be attributed to business practices of the health care industry. Is the industry moving at an appropriate pace to lower its carbon profile?  What additional actions can the pharmaceutical and biotech sector take to address the challenge? Do the standardized company reporting guidelines that allow the public to assess and compare progress on climate change act as an incentive or as a burden, in terms of doing more?  
      • Is the international negotiating framework now in place for addressing climate change sufficiently enabled to tackle the public health aspects of the threat? Are government negotiators sufficiently aware of the private-sector’s commitment and contributions to meeting climate-related targets?
      • Africa is a relatively poor continent which contributes marginally to global warming but whose livelihoods are disproportionally damaged by its effects.  What can the region’s experience tell us about what works and what doesn’t in addressing what is now an existential global challenge?  Is progress simply an issue of extracting more concessional aid through a revamp of the current international financing system?  What can we learn from local approaches built around community awareness and empowerment?  Can the continent achieve a better balance between exploiting abundant extractive industry resources and transitioning to greener, renewable technologies?    
      BPMs
      PANEL 2B
      BPMs

      9:05 AM - 10:05 AM

      BioPharma Pressure Points: PBMs, Pricing, Access, and the Global Supply Chain

      Chair

      Ezekiel J. Emanuel
      Vice Provost for Global Initiatives; Co-Director, Healthcare Transformation Institute; Diane v.S. Levy and Robert M. Levy University Professor; Perelman School of Medicine and The Wharton School; University of Pennsylvania

      PANELISTS
      Ariel Katz
      Co-founder and Chief Executive Officer, H1 
       
      Daniel Mendelson
      Chief Executive Officer, Morgan Health, JPMorgan Chase & Co. 
       

      John M. O'Brien
      President and Chief Executive Officer, National Pharmaceutical Council 

       

      Janet Woodcock
      Former Principal Deputy Commissioner, U.S. Food & Drug Administration

      Background and Topics for Discussion:

      Health care in the US continues to adapt to the structural weaknesses exposed by the Covid-19 pandemic.  Industry has responded with initiatives to consolidate market positions and test out new business models, all with the aim of mastering a moving chessboard of competitive challenges.  These include reducing cost exposures, realigning business operations to achieve the long-awaited “digital transformation” and fending off inroads from adjacent players seeking a foothold in an opportunity-rich sector that now accounts for almost one-fifth of US GDP.   

      Also demanding industry attention is the pandemic’s effect on government involvement in health care.  The Biden Administration has positioned access to health as a right, not a privilege, advancing an expansive post-Covid legislative agenda focused on lowering prescription drug costs and insurance premiums; enhancing coverage under the subsidized insurance marketplace option provided through the 2010 Affordable Care Act; more federal funding for the low-income federal-state Medicaid program; and an aggressive legal stance on anti-competitive behaviors. Still in play is a bipartisan congressional effort to impose more transparency on the business practices of the pharmacy benefit manager (PBM) segment that most private-sector employers rely on to manage drug benefit costs – and where three giant PBM companies now control 80% of the US market.

      Big pharma companies are uniquely exposed to provisions enacted in the 2022 Inflation Reduction Act (IRA) which, for the first time, grants the federal government’s Medicare program for seniors authority to negotiate with individual drugmakers the price of the most profitable and widely used branded medicines prescribed to patients.  This, in addition to a steep upward revision of drug manufacturers’ percentage-based cost-sharing contributions to reimbursement under Medicare, means that companies face a much more difficult (and ultimately less profitable) set of calculations in deciding whether to participate in a program that currently accounts for slightly more than half of overall prescription drug sales in the US.   The concern is that the growing weight of government on the industry will “bleed” to the employer-driven commercial payer side.

      Taken together, such changes carry the potential to shift US health care markets, policy and regulation in new, unanticipated directions. The big question for this moment is whether the industry playbook has changed as well.  

      Panelists will discuss these and other issues, including:   

      • Defining the new US healthcare and medicines innovation landscape in the aftermath of Covid-19. What has changed in the calculations required to deliver revenue growth and profitability to industry shareholders and meet the expectations of policy-makers and the public at large?  
      • Ways in which a soaring post-Covid public debt load and mounting federal spending deficits will shape the US health reform debate. What measures are needed to preserve current standards of patient care and fund new drug research and other drivers of medical innovation, where the US leads the world? Will the piercing of the $1 million per drug barrier for gene therapies lead to a more expansive interpretation of accessibility, one based on the lifetime value of a cure? 
      • How will the Biden Administration’s expanded government role in health care financing and delivery play out? Are the impacts of the sweeping 2022 IRA legislation on negotiated Medicare drug pricing sufficiently understood by industry and the public?
      • Viewed from another perspective, can the FDA maintain its independence as industry regulator in a drastically more politicized decision-making environment in Washington?
      • Most working Americans receive health care benefits through private-sector commercial insurance plans. What innovations are taking place in this sector to tackle rising employer cost contributions while maintaining the competitive benefits that workers expect?  Is the PBM controlled network pharmacy and formulary model down for the count?
      • There is an emerging bipartisan consensus to force more transparency on drug pricing and other, often opaque, commercial business practices within the industry overall. What impact will this year’s election have in charting the way forward – and what does it mean for the future of new drug development? Is the US longtime status as preferred first country of launch in jeopardy?
      • Geopolitical risk has emerged as a top issue for the biopharma C-suite – unanticipated disruptions in the global pharma supply chain is just one threat now on the table. What role should regulators and drug companies play in reversing the sharp rise in drug shortages (which reached a record high in the last quarter of 2023) that harm vulnerable patients?  What’s the next step toward joint risk management and regulatory harmonization across the entire supply chain, involving all the key country sources of medicines worldwide?
      • Hazard a guess:  will the US health system look more like those of western Europe in 2030?  Will investing decisions on US drug innovation remain in private-sector hands or in a more dispersed “social partnership” model? 
      COFFEE BREAK

      10:05 AM - 10:15 AM

      Chair
      Ken Frazier
      PRIX GALIEN AWARDS CEREMONY
      Ken Frazier

      11:45 PM - 12:30 PM

      Tribute to Bernard Poussot followed by awards ceremony for the categories: Best Medical Technology, Best Digital Health Solution, Best Incubator/Accelerator/Equity and Best StartUp

      MASTER OF CEREMONY

      Kenneth C. Frazier
      Prix Galien Committee Chair (Categories: Medtech, Digital Health, IAE and Startup); Retired Chairman and Chief Executive Officer, Merck & Co., Inc.; Chairman, Health Assurance Initiatives, General Catalyst 

      LUNCH BREAK

      12:30 PM - 1:00 PM

      Chair
      Big_Biotech
      PANEL 4A
      Big_Biotech

      1:00 PM - 2:00 PM

      Big BioTech - Where Is It Going?

      Chair

      Phillip A. Sharp
      Nobel Laureate; Galien Forum Co-Chair; Institute Professor and Professor of Biology Emeritus, Koch Institute for Integrative Cancer Research, MIT; Co-Chair of the Galien Forum

      PANELISTS
      Ray Dehaies
      Senior Vice President Global Research Emeritus, Amgen 
       
      Pushkal Garg
      Chief Medical Officer and Executive Vice President, Development & Medical Affairs, Alnylam

      Jane Grogan
      Executive Vice President and Head of Research, Biogen
       
      George D. Yancopoulos
      Board Co-Chair, President and Chief Scientific Officer, Regeneron

       

      Background and Topics for Discussion:
       
      One of the most important strategic shifts in the global medicines market is the significant role biotech companies now play through the entire cycle of new drug development, from initial target discovery to end-to-end commercialization and marketing. Small entrepreneurial enterprises launched by physician- scientists in the late 20th century aftermath of the DNA revolution have thrived. Today, these homegrown advocates of foundational science account for a major share of FDA approvals, particularly in emerging areas like regenerative medicine. As an example, just the four companies represented on this panel have within the past two decades brought to market no less than 15 world-class breakthrough-designated products; 14 of these each posted global “blockbuster” sales of more than $1 billion in 2023.

       

      However, what has worked well to date is no guarantee against the uncertainties exposed by a pandemic that no one predicted, eroded what used to be the consensus on the positive role of science in society, and revealed major shortcomings in public health and institutions that support innovation. Responses in the form of a tougher pricing environment will force a significant realignment of priorities toward reimbursements where payers have the momentum. The most innovative gene-based therapies will need to work harder to earn a predicable rate of return, balancing the promise of a cure against the enormous up-front overhead risks assumed by the originator company in safely delivering the therapy to what is often a very small cohort of patients. Building in the technology to make these cost manageable is crucial to the future of patients benefiting from gene-based interventions. A focus on raising operational efficiencies include risk-based capital allocation, financial resilience, talent retention as well as the distractions of replacing legacy data systems with a radical, more strategic approach to information management. An agenda like this sounds much like the path forced over the past few years on an over-bureaucratized “big Pharma:” it raises the question, can the two players – big bio and big pharma – be that far apart?

       

      Panelists will address these and other issues, including:

      • Evolution of the biotech business model since the founding of Genentech in 1976 to commercialize the nascent promise of recombinant DNA technology. Fifty years on, is drug biotech still an emerging industry in search of a sustainable revenue base? Is size, scale and reach the only feasible path to success in today’s era of expensive new science and growing payer consolidation?
      • Looking ahead to the end of this decade, what areas of biologic science applied to drug discovery offer the greatest potential in outcomes that are meaningful to patients and payers?
      • Can we expect AI-leveraged computation and large-scale data sets to serve as the cure-all to persistently high attrition rates in drug development? Or is it just one element in a larger scenario of progress?
      • Is VC and other investor funding streams aligned to the unpredictable payout cycles likely to occur in a fast-evolving therapeutic space? Is the government/regulatory community ready with the expertise, resources and policy commitments to incentivize private-sector risk in taking ground-breaking technologies to timely market approval, and beyond?
      • Managing the operational challenges of making breakthroughs in science more cost-effective, particularly in key areas like biologic drug manufacture and how novel platform therapies like Crispr can be delivered to patients in vivo. How soon will we move gene-editing and CAR-T cell therapy “over the finish line,” as the reliable standard of care for heritable diseases as well as for more common conditions?
      • Message to the next US Administration: what “big biotech” needs to keep succeeding for patients.
      OPENING_REMARKS_MUNIR_PIRMOHAMED
      OPENING REMARKS
      OPENING_REMARKS_MUNIR_PIRMOHAMED

      9:20 AM - 9:30 AM

      PRIX GALIEN UK COMMITTEE Chair

      Prof. Sir Munir Pirmohamed
      David Weatherall Chair of Medicine, University of Liverpool

      PANEL1_HTA_COLLABORATION
      PANEL 1
      PANEL1_HTA_COLLABORATION

      9:30 AM - 10:40 AM

      Advances in International HTA collaboration: How will joint clinical assessments impact patient access to medicines in Europe?

      Chair

      Dr. Mel Walker
      Life Sciences Strategic Advisor and CEO, Access InVivo

      PANELISTS

      European regulatory perspective
      Dr. Steffen Thirstrup
      Chief Medical Officer, European Medicines Agency

       

      European HTA perspective
      Niklas Hedberg
      Chief Pharmacist at the Swedish national governmental authority,
      the Dental and Pharmaceuticals Benefits Agency and Co-Chair, the EU Member States Coordination Group under HTAR

       

      UK HTA perspective
      Dr. Sam Roberts
      Chief Executive Officer, NICE

       

      European Patient perspective
      Valentina Strammiello
      Director of Strategic Initiatives at the European Patients Forum

       

      Global Industry perspective
      Dr. Greg Rossi
      Senior Vice President Oncology Europe and Canada, AstraZeneca

      PANEL2_INDIVIDUALISED_MEDICINE
      PANEL 2
      PANEL2_INDIVIDUALISED_MEDICINE

      11:00 AM - 12:10 PM

      Advances in Individualised Medicine: Are breakthrough therapies for ultra rare diseases within reach?

      Chair

      Dame June Raine
      Chief Executive Officer, Medicines and Healthcare products Regulatory Agency

      PANELISTS

      Research Perspective
      Prof. Matthew Wood
      Professor of Neuroscience, Deputy Head Medical Sciences Division (Innovation), University of Oxford; Director and Chief Scientific Officer Oxford-Harrington Rare Disease Centre; Adjunct Professor of Medicine, Case Western Reserve University School of Medicine

       

      Industry Perspective
      Dr. Gregory Friberg
      Chief Research & Development Officer, BioMarin Pharmaceutical

       

      Regulatory Perspective
      Dr. Janet Woodcock
      Former Director of the Center for Drug Evaluation and Research and Principal Deputy Commissioner of the U.S. Food and Drug Administration

       

       

      The Association of the British Pharmaceutical Industry Perspective
      Dr Dan O’Connor
      Director Regulatory and Early Access Policy, The Association of the British Pharmaceutical Industry

       

      European Patient Perspective
      François Houyez
      Director of Treatment Information and Access, Senior Policy Advisor, EURORDIS

      KEYNOTE_ARA_DARZI
      KEYNOTE
      KEYNOTE_ARA_DARZI

      12:55 PM - 1:45 PM

      Prof. Ara Darzi, Baron Darzi of Denham, Paul Hamlyn Chair of Surgery and Co-Director of the Institute of Global Health Innovation at Imperial College London

      Keynote

      Prof. Ara Darzi,
      Baron Darzi of Denham
      Paul Hamlyn Chair of Surgery and Co-Director of the Institute of Global Health Innovation at Imperial College London



      KEYNOTE_TONY_WOOD
      KEYNOTE
      KEYNOTE_TONY_WOOD

      12:55 PM - 1:45 PM

      Dr. Tony Wood, Chief Scientific Officer, GSK

      Keynote
      Dr. Tony Wood
      Chief Scientific Officer, GSK


      PANEL3_OBESITY
      PANEL 3
      PANEL3_OBESITY

      1:45 PM - 2:45 PM

      Advances in Treatment for Obesity and its Co-Morbidities: Global Challenges and Opportunities for Prevention and Population Health

      Chair

      Prof. Naveed Sattar
      Professor of Cardiometabolic Medicine, University of Glasgow, and Chair of Obesity Healthcare Goals Programme

      PANELISTS

      Clinical Perspective
      Prof. Simon Griffin
      Professor of General Practice, Group Leader in the Medical Research Council Epidemiology Unit, University of Cambridge​

       

      European Patient Perspective
      Vicki Mooney
      Executive Director, European Coalition for People living with Obesity​

       

      Global Industry Perspective
      Prof. Rachel Batterham
      Senior Vice President of International Medical Affairs, Eli Lilly and Company

       

      Global Research Perspective
      Prof. Melanie Davies
      Professor of Diabetes Medicine, University of Leicester; Co-chair of EASD/ADA

      PANEL4_MENTAL_HEALTH
      PANEL 4
      PANEL4_MENTAL_HEALTH

      3:05 PM - 4:15 PM

      Advances in Treatment of Symptoms in Mental Health/Mood Disorders: How can healthcare systems deliver solutions at scale to address the global mental health crisis?

      Chair

      Prof. Kathryn Abel
      Mental Health Mission Co-Chair; European Research Council Fellow and National Institutes of Health Research Senior Investigator​

      PANELISTS

      Lived Experience Perspective
      Dr. Vanesa Pinfold
      Co-Founder/Research Director, McPin Foundation and Chair of the Alliance of Mental Health Research Funders​

       

      Global Industry Perspective
      Catherine Owen Adams
      Chief Executive Officer, Acadia Pharma

       

      Global Digital Health Perspective
      Sanket Shah
      President & Board Member, Otsuka Precision Health

      Academic Perspective
      Prof. Michael Browning
      Lead of Mood Disorders Translational Research Collaboration, Honorary Consultant Psychiatrist and Professor of Computational Psychiatry at the University of Oxford

       

      Futurist Perspective
      Andrew Grill
      Actionable Futurist and Bestselling Author of Digitally Curious

      KEYNOTE_LAWRENCE TALLON
      KEYNOTE
      KEYNOTE_LAWRENCE TALLON

      4:15 PM - 5:00 PM

      Lawrence Tallon, Chief Executive Officer of the Medicines and Healthcare products, Regulatory Agency (MHRA)

      Keynote

      Lawrence Tallon
      Chief Executive Officer of the Medicines and Healthcare products, Regulatory Agency (MHRA)



      CLOSING_REMARKS
      CLOSING REMARKS
      CLOSING_REMARKS

      5:00 PM - 5:15 PM

      PRIX GALIEN COMMITTEE Chair

      Pr Sir Munir Pirmohamed
      David Weatherall Chair of Medicine, University of Liverpool

      AWARDS

      Prix Galien UK Awards Ceremony

      AWARDS
      Natural History Museum, London

      7:30 PM

      KOL

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