{"id":49611,"date":"2015-04-24T00:00:00","date_gmt":"2015-04-23T23:00:00","guid":{"rendered":"http:\/\/www.pcb.ub.edu\/is-flexible-planning-possible-in-clinical-development\/"},"modified":"2020-11-18T14:55:58","modified_gmt":"2020-11-18T13:55:58","slug":"is-flexible-planning-possible-in-clinical-development","status":"publish","type":"post","link":"https:\/\/www.pcb.ub.edu\/en\/is-flexible-planning-possible-in-clinical-development\/","title":{"rendered":"Is flexible planning possible in clinical development?"},"content":{"rendered":"<p>The second session of Lessons Learned \u2013organized by\u00a0Biocat\u00a0and\u00a0<a href=\"http:\/\/cataloniabio.org\/\" target=\"_blank\" rel=\"noopener noreferrer\">CataloniaBio<\/a>\u2013 was a total success, with more than 50 participants from pharma companies, biotech SMEs, health consultancies and hospitals. Over the 4-hour session, experts \u2013moderated by\u00a0<a href=\"http:\/\/www.vcnbiosciences.com\/\" target=\"_blank\" rel=\"noopener noreferrer\">VCN Biosciences<\/a>\u00a0CEO\u00a0Manel Cascall\u00f3\u2013 expressed their points of view and explained their experience with the questions your must ask yourself and how to approach the design of this complex development process in order to make yourself attractive to capital investors and benefit society.<\/p>\n<p>Gemma Estrada, director of the Biocat Barcelona Clinical Trials Platform (BCTP), spoke about the new tools and technology that allow researchers to accumulate data from different origins, and to interpret and exploit the information more quickly and efficiently. She also highlighted the importance of resolving \u2013when designing a study- the 3P needs: patients, payers and promoters.<\/p>\n<p>Additionally,\u00a0Josep Llu\u00eds Falco, senior manager at\u00a0<a href=\"http:\/\/www.antares-consulting.com\/es_ES\/\" target=\"_blank\" rel=\"noopener noreferrer\">Antares Consulting<\/a>, explained that strategy comes first; developing a plan is second. It is important to start off with a good strategy and then, above all, to have a feasible clinical design in mind.<\/p>\n<p>Joan Perell\u00f3, CEO and founder of Laboratoris\u00a0<a href=\"http:\/\/www.sanifit.com\/web\/\" target=\"_blank\" rel=\"noopener noreferrer\">Sanifit<\/a>, discussed the impact designing a clinical plan has on attracting investment and explained the \u201cimportance of finding a segment of the population to do a quick proof of concept.\u201d<\/p>\n<p>Participants also had the opportunity to hear from\u00a0<a href=\"http:\/\/www.trifermed.com\/\" target=\"_blank\" rel=\"noopener noreferrer\">Trifermed<\/a>\u00a0CEO\u00a0Sergi Trilla\u00a0about the lessons learned through real partnering cases at different stages of development. Trilla highlighted the importance of having clear ideas on several issues: a value-based business model that addresses a market need; understanding market forces and main trends; and finding a good partner to help create and attract value, as well as the advantages of internationalization.<\/p>\n<p>Finally,\u00a0Ra\u00fcl Insa, CEO of\u00a0<a href=\"http:\/\/www.sombiotech.com\/\" target=\"_blank\" rel=\"noopener noreferrer\">SOM Biotech<\/a>, pointed out three important aspects to take into account when creating a good clinical development plan: not losing sight of what the client wants and being rigorous in regulatory compliance and creative in design.<\/p>\n<p>Sharing experiences to boost competitiveness<\/p>\n<p>The Lessons Learned sessions are a knowledge and networking forum geared towards professionals from companies in the life sciences arena. They aim to be a place to share experiences and reflections on the different strategic areas of knowledge and skills needed to boost the competitiveness of biotechnology companies.<\/p>\n<p>Four more sessions will be held in 2015 covering various topics: IP and strategy (21 May), Negotiating with investors and licensing (9 July), Taxation and MAB crowdfunding (8 October) and Nutraceutics (12 November).<\/p>\n","protected":false},"excerpt":{"rendered":"<p>The importance of a solid clinical development plan and the possibility of shortening it or making it cheaper \u2013in addition to the various collaboration models to fund clinical trials- and the role of partnering were some of the topics discussed by experts and professionals from the sector, debating and sharing experiences at the\u00a0Lessons Learned\u00a0session held on Tuesday at the\u00a0Parc Cient\u00edfic de Barcelona\u00a0(PCB).<\/p>\n<p>\u00a0<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"inline_featured_image":false,"footnotes":""},"categories":[8],"tags":[],"class_list":["post-49611","post","type-post","status-publish","format-standard","category-uncategorized"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Is flexible planning possible in clinical development? 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