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CORDIS - Resultados de investigaciones de la UE
CORDIS

Boosting the reduction of the environmental impact of pharmaceutical products throughout their entire life cycle.

CORDIS proporciona enlaces a los documentos públicos y las publicaciones de los proyectos de los programas marco HORIZONTE.

Los enlaces a los documentos y las publicaciones de los proyectos del Séptimo Programa Marco, así como los enlaces a algunos tipos de resultados específicos, como conjuntos de datos y «software», se obtienen dinámicamente de OpenAIRE .

Resultado final

Report on the standardization landscape and applicable standards (se abrirá en una nueva ventana)

Report summarizing the relevant standardization landscape and appliable standards

Roadmap for adoption of PAT and Digital Twin Technologies (including regulatory compliance requirements) (se abrirá en una nueva ventana)

Report that will consist in a summary review of SoA of PAT and Digital Twin adoption in European Pharmaceutical industry; a SWOT analysis to feed into an Opportunities Roadmap that also takes account of the regulatory hurdles, as well as recommendations for a favorable/enabling regulatory framework, without compromising safety.

"Concept paper on ""compliance-by-design"" key-drivers and roadmap of the possible regulatory pathways or relevant regulatory frameworks for the required ""compliance-by-design"" strategies" (se abrirá en una nueva ventana)

Concept paper that reviews the latest developments in the scientific review, regulation, and marketing authorization procedures in the respective fields (related to the ETERNAL technological processes and developments) to inform a ‘compliant-by-design’ strategy in relation to the developments as part of the ETERNAL cocreation process.

Report on the contribution to standardization (se abrirá en una nueva ventana)

Report outlining the contribution the project has/will make to standards.

Research roadmap and inventory of tools for the integration of existing knowledge into pharma risk assessment (se abrirá en una nueva ventana)

Public report that documents a research roadmap for the integration of scientific and regulatory knowledge into pharmaceutical risk assessment for fate modelling, bioavailability assessment and receptor identification, for regulatory testing and assessment, and inventory of tools for the integration of existing knowledge into pharma risk assessment.

Publicaciones

Project Eternal Overview Presentation (se abrirá en una nueva ventana)

Autores: Ferrer Pérez, Pablo; Sebastia-Luna, Paz; Henderson, John
Publicado en: 2025
Editor: ZENODO
DOI: 10.5281/ZENODO.10688671

A New Collaboration to Establish Safe and Sustainable Pharmaceutical Lifecycles by Design (se abrirá en una nueva ventana)

Autores: Henderson, John; Peeling Robert
Publicado en: 2025
DOI: 10.5281/zenodo.10788903

Organic Solvent Nanofiltration in Pharmaceutical Applications (se abrirá en una nueva ventana)

Autores: Xiaoa, Hui; Feng, Yanyue; Goundry, William R.F.; Karlsson, Staffan
Publicado en: Organic Process Research and Development, 2024, ISSN 0000-0000
Editor: American Chemical Society
DOI: 10.1021/acs.oprd.3c00470

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