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DTSTART;TZID=Europe/Rome:20240111T103000
DTEND;TZID=Europe/Rome:20240111T113000
DTSTAMP:20260410T232019
CREATED:20231219T101506Z
LAST-MODIFIED:20231219T101506Z
UID:11428-1704969000-1704972600@biopmed.eu
SUMMARY:Intellectual Property Rights (IPR) and Management
DESCRIPTION:🚀 Join us for the 3rd webinar of our Health InnoFacilitator series on Intellectual Property Rights (IPR) and Management. Whether your field is healthcare\, legal\, or innovation\, this webinar will help you understand how to effectively manage intellectual property in collaborative healthcare projects. \nEnhance your understanding of contract issues and protect intellectual property in the dynamic world of health innovation. \n🌐 Topic: “IPR Management: Contractual Issues in the Context of Open Innovation and Other Co-creation Tools” \n🗓 Date: 11 January 2024 🕥 Time: 10:30 – 11:30 AM \n🎙 Lecturers: \n\nValentina Gazzarri\, Lawyer in Intellectual Property at BUGNION SpA\nElisabetta Guolo\, Lawyer and Consultant in Trademarks and Designs at BUGNION SpA\n\n🔗 Sign up here: https://lnkd.in/dZtnEmT6
URL:https://biopmed.eu/en/evento-en/intellectual-property-rights-ipr-and-management/
LOCATION:Online
CATEGORIES:bioPmed events
ATTACH;FMTTYPE=image/jpeg:https://biopmed.eu/wp-content/uploads/2023/12/1702462669182.jpeg
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DTSTART;TZID=Europe/Rome:20240123T110000
DTEND;TZID=Europe/Rome:20240123T120000
DTSTAMP:20260410T232019
CREATED:20240109T114013Z
LAST-MODIFIED:20240214T143330Z
UID:11426-1706007600-1706011200@biopmed.eu
SUMMARY:MDR & IVDR certification: where are we?
DESCRIPTION:During the meeting we will discuss regulatory updates regarding the registration process of medical devices (MDR) and in particular in vitro medical devices (IVDR). We will discover the necessary steps to submit certification requests to notified bodies (NB) proposing winning strategies to keep up with the deadlines set by Regulation 2023/607. Finally\, we will provide an overview of the current European situation.\nRegister \nTarget group\n\nQuality and RA Manager\nR&D\nCompany managers\n\nWhat we learn from the webinar\n\nIVDR – current situation Italian market and NB\nMDR focus on Regulation 2023/607 – MDD extension mode\nTesting active medical devices – activity promotion IMQ laboratories\nHow IMQ wants to support companies in keeping up with the times: IMQ MED UP\n\nProgram\nWe will talk about the current regulatory situation at the beginning of 2024 on the subject of IVDR and MDR to understand the critical issues and necessary actions to be taken to comply with the deadlines dictated by Regulation 2023/607. It is essential to understand the stages within which manufacturers must send applications to the NB and the European situation.\nSpecifically we will talk about the Active medical device world to treat the continuous regulatory update of the standards for electrical safety and electromagnetic compatibility and what IMQ laboratories can offer.\nThis is linked to the new format launched by IMQ (IMQ MED UP) with the aim of offering a tool to companies to stay up to date in the regulatory field. \nLecturer\nAndrea Santoleri. Andrea Santoleri is the current Sales Manager of the Medical Devices Division of IMQ Spa.\nBiomedical engineer\, he graduated from Politecnico di Milano with a specialization in Cells\, Tissues and Biotechnology and a thesis at the University of Arizona in the field of microfluidics. \nRegister
URL:https://biopmed.eu/en/evento-en/mdr-ivdr-certification-where-are-we/
LOCATION:Online
CATEGORIES:bioPmed events
ATTACH;FMTTYPE=image/png:https://biopmed.eu/wp-content/uploads/2024/01/MDRIVDR.png
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