Thought Leader Interview: Dr Tõnu Esko, PhD, is Deputy Director of Research, Estonian Biobank, Estonian Genome Center, University of Tartu.

March 8, 2016 If you can gather all this data together – from historical data i.e. disease history, to the ‘omics’ data and genetic data – we could, for instance, develop a web-based service where patients could see how their past and current lifestyle decisions affect their disease risks. For example, if a patient knows he has a higher risk for smoking-induced cancer, that might motivate him to stop smoking – or if he has a genetic tendency to become obese in later life, then maybe that will motivate him to follow a healthier lifestyle.

Thought Leader Interview: Janet Addison, Senior Manager & Product Lead, Centre for Observational Research at Amgen

March 8, 2016 Patient data, at the end of the day, belongs to individual people. We are sensitive to that and I think having the input of an independent external ethical advisory board shows just how careful we are being, which is important for the public to know. Having convened that group and meeting with them regularly is a very big step forward.

RWE and Health Data in the EU: viable public policy vs. political overreach


February 7, 2016
When asked about the issues around harnessing health data in Europe in Washington DC on October 27th, Prof Hans Georg Eichler, Senior Medical Officer of the European Medicines Agency responded, "I come from an area with hysterical data protection.”[1] Why would a regulator feel this way? Surely, Europe’s public health systems have access to health data that is second to none?

Thought Leader Interview: Bart Vannieuwenhuyse, Senior Director Health Information Sciences, Janssen Pharmaceutica; Coordinator EMIF


January 27, 2016
When it comes to sharing health data, solving the technical solutions of data sharing is more straightforward than structuring workable collaboration models that satisfy both data owners and researchers alike, says Bart Vannieuwenhuyse, Senior Director Health Information Sciences, Janssen Pharmaceutica; Coordinator EMIF.

4th EMA-EBE joint Regulatory Policy Seminar: Emerging Medicinal Products – from Laboratory to Patient use


December 14, 2015
Europe’s world-leading science base is fuelling innovation in advanced therapies, which a growing volume of clinical data indicates will address a diversity of unmet medical needs, delivering better health and generating economic benefits.



Interview with Keith Thompson, CEO of the UK Cell Therapy Catapult: Advanced therapies stand poised to change the drug discovery and development paradigm


November 25, 2015
After years of painstaking research, cell, gene and tissue therapies are turning in unprecedented evidence of efficacy in phase I/II. Unlike the old model, where the sole focus would now be on phase III, companies need to work simultaneously on manufacturing, logistics, pricing and getting the product to the patient, says Keith Thompson.

Views from Eduardo Bravo of TiGenix: Allogeneic stem cell therapy makes a breakthrough in the clinic and is poised to address unmet medical need


November 25, 2015
Positive data in the phase III trial of TiGenix’s Cx601 allogeneic cell therapy indicates it could provide a one-off treatment for complex perianal fistulas, a complication of Crohn’s disease. The results open up a completely new avenue for treatment of patients who do not respond to existing therapies, says Eduardo Bravo, CEO of Tigenix.

Interview with Emil Pot, co-founder of ActoGeniX: Europe needs larger investment funds to create a funding escalator from phase II to phase III


November 19, 2015
With more companies advancing innovative therapies to the end of phase II, the funding requirements of European biotech are spiralling. A new initiative is required to create large and liquid funds to support the next stage of growth and ensure Europe reaps the benefits – both medical and commercial – of its excellent research, says Emil Pot.

Report from the Alliance for Regenerative Medicine (ARM) Investor Day in London: As cell and gene therapies turn in positive clinical data, attention turns to delivery to patients


November 12, 2015 - London
After huge investment in the basic science and translation to the clinic, Europe’s advanced therapies companies are accumulating data, which indicate these products have an unprecedented effect. Now effort is needed to develop manufacturing, organise logistics, agree reimbursement and ensure patients get the benefits. Vital Transformation reports for EBE from the ARM Conference.

Press Release: Better Science, Better Health Conference to Promote International Collaboration to Accelerate New Models in Healthcare


October 22, 2015 – Washington D.C.
Vital Transformation is pleased to announce the Better Science, Better Health: New Healthcare Models Conference, which aims to promote international collaboration to accelerate new models in healthcare. Taking place in Washington D.C., from 27-28th October, the Conference features thought leaders who will help shape the future of healthcare in both Europe and the United States.

Go to Top