Pharmaceutical and biotechnology products eligible to be evaluated by Prix Galien Greece Award must be built on innovation and developed by chemical, biological or biotechnological methods with details and accuracy in their specifications for the production process and clinical trials\u2019 results. Products nominated for the awards must be marketing authorized (for treatment indication-not necessarily priced<\/strong>), in Greece (through a central, national process or by mutual recognition) until December 31, 2020<\/strong>\u00a0and up to four (4) past calendar years (01\/01\/2017-31\/12\/2020). With regard to the category best medical technology product<\/strong>, in order to be nominated for the awards, their date of marketing authorization in Greece must be until December 31, 2020<\/strong>\u00a0and up to two (2) past calendar years (01\/01\/2019-31\/12\/2020).<\/p>\n Quality Criteria<\/strong><\/p>\n Candidate medicinal products can belong to any therapeutic category. However, the awards shall be bestowed to those which contribute to the improvement of the quality of life or save lives, on the basis of two criteria:<\/p>\n 1. Which was the innovation during the course of the product\u2019s scientific development, the way it acts and its clinical use? Each awarding category shall declare only one winner, however, in the case of a tie in votes of one or more nominees, the judging committee reserves the right to designate a second Hors Prix winner.<\/p>\n <\/p>\n The right to participate in this category have both orphan and non-orphan products approved in the European Union, that have only rare disease indication and are being marketed in Greece.<\/p>\n Candidates\u2019 Summary<\/strong> (up to 1 page) Formatting<\/strong><\/p>\n The total number of pages of each submission in the category in question must not exceed 12\u00a0\u03914 size pages, 1 \u00bd spaced with 12-point Arial type fonts and 2 cm margins.<\/p>\n All documents\/certificates must be submitted on-line<\/strong> together with the participation application.<\/em><\/p>\n For more information regarding the application fee and the sumbission amenities of the\u00a0\u201cBest Orphan Drug (Rare Disease)\u201d<\/strong>, please contact us on\u00a0admin@jpcom.gr<\/strong>\u00a0or call us on\u00a0210-8132828, 210-8132366.<\/strong><\/p>\n
\nThe above category also includes older medicinal products approved for a new innovative treatment indication or a new therapeutic entity (NTE) incorporated, however, in the past four (4) years.<\/p>\n
\n2. Which is the benefit for the future of medical science from the introduction of the product in clinical practice?<\/p>\nSPECIAL PARTICIPATION CRITERIA FOR GREECE<\/h3>\n
\nThis must be a brief summary mentioning the principal treatment indications of the product and the essential content of its proposal for nomination.
\nConcept<\/strong> (up to 3 pages)
\nThis should include :
\n\n
\nThis should outline:
\nExecutive summary of clinical development program, including key facts of mechanism of action, dose-finding and trial design.
\nThe application should not provide information for more than 10 publications (peer-reviewed)
\nConclusions<\/strong> (up to 1 page)
\nThis section is not obligatory but applicants may wish to include conclusions about the merits of the product.<\/p>\nFEE FOR APPLICATIONS<\/h3>\n