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Browsing the "CASMI Views" Category

Reflections on a Health Crisis

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Ebola is worrying, very worrying. The worst outbreak of recent times has taken thousands of lives in four West African countries and the virus has begun to appear in the US and Europe – and in one case transmitted to a local healthcare worker. The death rate from this terrible [...]

October 13, 2014 Andrea Hodgetts CASMI Views 0

How to Succeed at Open Innovation – Rosie Pigott’s Blog for Wellcome Trust

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Blog repost from the Wellcome Trust. Read the original article here Today we launch “Shaping the Future of Open Innovation: A practical guide for life sciences organisations”, a new resource created by a collaboration led by the Wellcome Trust, the Centre for the Advancement of Sustainable Medical Innovation (CASMI) and Kinapse.Rosie Pigott from CASMI, [...]

September 4, 2014 Andrea Hodgetts CASMI Views 0

“We are gradually going to move away from fully fledged HTAs towards more European collaboration.”

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National associations throughout Europe are engaging with governments in a whole new way. At a recent Eyeforpharma event, Richard Bergstrom, Director General of EFPIA, spoke about: – How the regulatory model is changing – The benefits of sharing expectations and the strengths and weaknesses of company data with regulators, payers and patients [...]

August 13, 2014 Andrea Hodgetts CASMI Views 0

Putting Patients at the Heart of Medical Innovation

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It’s time that we truly put patients at the heart of medical innovation. When I say that, I don’t mean adding a token patient to a conference speaker panel or ‘box ticking’ that a pharmaceutical company has consulted a patient group. What I mean is that we need to completely [...]

June 10, 2014 Andrea Hodgetts CASMI Views 0

CASMI Fellow Speaks about ‘Patient Participation in Melanoma Clinical Research’

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CASMI Associate Fellow Dr Sarah Garner spoke at the Joint M-icab/ESO Conference in Brussels last weekend. Upon a joint invitation from m-icab, (Melanoma Independent Community Advisory Board), and ESO, (European School of Oncology) about 90 stakeholders – Melanoma patients and advocates, clinicians, representatives from the regulatory and Health Technology Assessment [...]

April 4, 2014 Andrea Hodgetts CASMI Views 0

Podcast: Reaching a Personalized Medicine Milestone

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With the recent news that Illumina’s latest sequencers have broken the $1,000 genome barrier, there’s great anticipation about the acceleration of personalized medicine. The Burrill Report spoke to Ed Abrahams, president of the Personalized Medicine Coalition, about the significance of the milestone, the move of whole genome sequencing to the [...]

February 4, 2014 Andrea Hodgetts CASMI Views 0

Tufts study: Data suggest breakthrough therapy designation meets goals

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Nearly 18 months after its launch by the FDA, the breakthrough therapy designation (BTD) is showing the potential to meet the agency’s stated goal of speeding the development and review of drugs that show early evidence of offering substantial improvement over existing therapies on a clinically significant endpoint. By approving [...]

February 4, 2014 Andrea Hodgetts CASMI Views 0

Podcast: Pharma Faces Shrinking Returns from Innovation

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The biggest pharmaceutical companies are successfully bringing new products to market, but are struggling with diminishing returns on investment, according to a new report from Deloitte and Thomson Reuters. The Burrill Report spoke to Neil Lesser, principal of life sciences strategy for Deloitte, about the industry’s efforts to remake R&D, [...]

December 11, 2013 Andrea Hodgetts CASMI Views 0

FDA on Personalised Medicine

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Stratified Medicine (personalising treatments to distinct patient populations) is the topic of this week’s BioCentury videocast. The FDA recently approved Illumina’s Next Generation Sequencing Technology, which rapidly and affordably sequences a patient’s genome, allowing doctors to make tailored treatment decisions after a single test. Following this decision, FDA Commissioner Margaret [...]

November 25, 2013 Andrea Hodgetts CASMI Views 0

Cut EU Red Tape: Report from the Business Taskforce

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CASMI contributed to the latest report from the Business Taskforce written for British Government, which calls for cutting red tape in clinical trials and making flexibilities in licensing more visible. This is particularly relevant for our Adaptive Licensing project, which uses existing legislation to grant patients earlier access to new medicines, [...]

October 17, 2013 Andrea Hodgetts CASMI Views 0