Second Health Technology Assessment (HTA) Conference

Date(s) And Time(s):
Nov 4 2010 8:00AM - Nov 5 2010 5:30PM

Location:
Radisson Blu Hotel Paris Charles De Gaulle Airport
Rue de La Chapelle
77990 Le Mesnil Amelot, Paris
France

Interest Area(s):
Comparative Effectiveness/Health Technology Assess,Regulatory Affairs,Research & Development

Overview:

Key Topics
• Mapping the HTA Landscape in Europe
• Risk-sharing Schemes and Conditional Reimbursement
• Methodologies to Generate the Right Data
• Building “Benefit Management Plans”

Overview
The Health Technology Assessment (HTA) landscape in Europe is currently under the spotlight more than ever before. It is changing, evolving and is in an increasingly dynamic state of flux, as agencies here and globally try to figure out the right pathway forward to ensure that the right treatments are made available to patients in sustainable healthcare frameworks.

HTA is also increasingly, therefore, becoming the focus of the stakeholders involved all stages of the medicines development process. Patients are proactively engaging with evaluators and payers. Innovative medicines manufacturers are working to build understanding of the value of their products – not only value to the patients, but also to the healthcare systems and to society as a whole. Decision-makers in the countries, whether they are governments or payers, are working to understand how to evaluate whether what they are paying for is worth the price-tag that is being asked. And, increasingly, countries are working together to create a more coordinated HTA assessment model.

The time is more than ripe to start figuring out how all of these different forces are going to work together in practice, and what the resulting outcomes will mean for patients, innovators, governments and payers alike. Because, while 10 years ago, the EU created a single market in reviewing and approving medicines from a clinical scientific perspective to facilitate uniform access to European patients, increasingly the subsequent scientific evaluation of the value of a product is now fragmented into different methodologies and different approaches post-approval. This means that, if we are to continue to realise the concept of a single EU and to support equity between patients in Europe, something must be do to have some degree of similarity in the approach.

The question is – how is all this going to be achieved and in what framework? Where are the multiple cooperative and EU-coordinated projects in HTA going? And how can we ensure that they do achieve this ultimate aim of getting needed, innovative treatments to the waiting patients?

This workshop will bring together all stakeholders – from regulators to governments, from national competent authorities to the European Medicines Agency in London and from industry, payers and – the ultimate beneficiary of a successfully functioning system – the patients who stand to benefit from the fruits of innovative R&D. The objective is to move from a “What is happening?” to “How will we make this ‘what’ into a functioning reality that achieves the multiple different objectives from all involved stakeholders?”

Target Audience:
The aim of this one and a half day conference is to bring together professionals working in the following areas:
• Pharmacoepidemiology / Quality of Life / Health Economics / Outcomes Research /Managed Healthcare
• Public Policy / Law
• Regulatory Affairs / Policy / Drug or Device Approval
• Clinical Research and Development
• Research and Development / Strategic Issues
• Government

Event Code:
10111

Contact Information:
DIA EUROPE
PHONE: +41 61 225 51 51
FAX: +41 61 225 51 52

E-MAIL: DIAEUROPE@DIAEUROPE.ORG

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