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CORDIS - Forschungsergebnisse der EU
CORDIS

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

CORDIS bietet Links zu öffentlichen Ergebnissen und Veröffentlichungen von HORIZONT-Projekten.

Links zu Ergebnissen und Veröffentlichungen von RP7-Projekten sowie Links zu einigen Typen spezifischer Ergebnisse wie Datensätzen und Software werden dynamisch von OpenAIRE abgerufen.

Leistungen

Report on the standardization landscape and applicable standards (öffnet in neuem Fenster)

Report summarizing the relevant standardization landscape and appliable standards

Roadmap for adoption of PAT and Digital Twin Technologies (including regulatory compliance requirements) (öffnet in neuem Fenster)

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" (öffnet in neuem Fenster)

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 (öffnet in neuem Fenster)

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 (öffnet in neuem Fenster)

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.

Veröffentlichungen

Project Eternal Overview Presentation (öffnet in neuem Fenster)

Autoren: Ferrer Pérez, Pablo; Sebastia-Luna, Paz; Henderson, John
Veröffentlicht in: 2025
Herausgeber: ZENODO
DOI: 10.5281/ZENODO.10688671

A New Collaboration to Establish Safe and Sustainable Pharmaceutical Lifecycles by Design (öffnet in neuem Fenster)

Autoren: Henderson, John; Peeling Robert
Veröffentlicht in: 2025
DOI: 10.5281/zenodo.10788903

Organic Solvent Nanofiltration in Pharmaceutical Applications (öffnet in neuem Fenster)

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

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