Latest project updates
- Improvements needed in recording brand and batch numbers for biological medicines to ensure patient safety
- New Leading Article about the challenges and opportunities for the traceability of (biological) medicinal products
- Disconnect between European and national regulation major barrier for advancing innovative medical therapies
Escher was launched in 2007 by TI Pharma – now Lygature – with the aim of helping to bring about a more efficient and effective regulatory system. It offers an independent research platform, with a pan-European focus, that promotes multi-stakeholder dialogue.
18+
scientific publications
16
PhD theses published
The Escher platform
Escher’s mission is to promote research and international debate in the field of policy and regulations, relating to development, market authorization, reimbursement, and use of medicines and medical technology. To this end, Escher initiates and conducts its own research into regulatory and health technology assessment topics. The platform also plays an active role in assignments undertaken by Lygature for external parties, for example within the ADAPT SMART project. In all cases, outcomes are translated into publications and/or practical proposals for regulatory and policy innovation, in order to facilitate patient access to medicines that address public health needs.
Providing neutral ground for multi-stakeholder dialogue and research
Scientific research and collaboration between public and private partners have been essential to Escher from the start. The platform reaches out to many different stakeholders, with partners from industry academia, government, NGOs and elsewhere. The broad range of activities that TI Pharma provided to support multi-stakeholder dialogue and research will be continued under the Lygature brand from January 2016, and include:
- Governance and coordination. Lygature is the legal entity responsible for the Escher platform and provides the chair of the Steering Committee, which decides whether and how a research project should be executed. Lygature also involves Escher when coordinating third-party assignments on regulatory topics, such as ADAPT SMART.
- Research activities. The Escher platform can offer an independent perspective on policy and regulatory topics. It initiates and conducts research projects, such as ‘Improving the EU system for marketing authorization’ and ‘Traceability of biologics’ (both now completed).
- Platform for dialogue. Lygature allows Escher to provide a multi-stakeholder home for regulatory innovation. The platform promotes dialogue on relevant policy topics, fueled by the evidence generated during research projects.
Escher is a unique platform that brings together a wide variety of stakeholders in strategic policy projects and research initiatives. It generates benefits by applying an understanding of both scientific and regulatory issues. Escher is a significant component in the wider Lygature mission to coordinate multi-stakeholder dialogue, and to help create more efficient and effective regulatory system.
Current projects
Escher is currently working on one large project, executed in collaboration with research institutions in the Escher network and supported by expertise and data from public and private stakeholders. Still more projects are progressing through the planning phase.
Completed projects
In order to maintain a strategic focus, Escher concentrates on projects that align with four main research themes. Within each main theme, a number of projects have been completed:
- The UK BIO-TRAC study: An evaluation of product and batch traceability in UK clinical practice and reporting of adverse drug reactions
- Evidence generation methods and evidence requirements
- Scientific dialogue and stakeholder interaction
- The decision-making process and benefit-risk assessment
- Evaluating the regulatory system
Outputs from Escher
Escher is focused not only on generating new evidence, but also on disseminating it as effectively as possible. The goal is always to do everything possible to help translate research findings into real-world regulatory improvements, creating benefits for patients.
Results are therefore presented in many different ways. These include formal scientific papers in leading journals and PhD theses, but they extend much further. Events are hosted to encourage face-to-face discussion, policy reports are written to stimulate debate and press releases raise awareness of the progress made in the projects.
Project updates
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TI Pharma coordinates European research project on market access of innovative medicines
Innovative medicines may be brought to patients faster. How this can be achieved is investigated by ADAPT SMART, a public-private partnership between 32 European partners with funding from the Innovative Medicines Initiative. The project that launched last week is coordinated by the TI Pharma platform for regulatory innovation 'Escher'.
Click here for the press release (in Dutch).
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Workshop Report - Pharmacovigilance of Biologics
On the 20th of May, Escher hosted a workshop in Amsterdam to address current challenges in the brand name/batch traceability of biologics in clinical practice. The report highlights the key findings from the discussions and possible ways forward.
Read the report here.
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Escher will present at the DIA Euromeeting, 13 – 15 April 2015
Escher has been invited to present at the 27th Annual Euromeeting to be held from 13 – 15 April 2015 in Paris (http://www.diahome.org).
In Theme 5 (Collaborative consortia, IMI and the Way to Horizon 2020) André Broekmans, director of the Escher Platform will give a talk on “Collaborative learning from the Regulatory System of Medicines. Results from the Escher Project” on Tuesday 14 April and he will participate in a panel discussion with public-private partnership stakeholders on Wednesday 15 April.