Keep abreast with law & ethics aspects at the frontiers of health & life science innovation: Join the Inter-CeBIL Master Class!
This course is a part of
What awaits you?
- Explore groundbreaking advances: From AI-powered diagnostics to gene editing, we will discuss the latest health and life science breakthroughs.
- Keep up with regulations: Legislative initiatives like the EU AI Act are reshaping the landscape. Learn how to adapt and thrive.
- Embrace sustainability matters: Discover how health and life science innovation can be economically viable, responsible, and foster inclusivity.
Why choose Inter-CeBIL?
- Leading Expert Instructors: Learn from teachers from prestigious institutions, including the Universities of Copenhagen, Cambridge, Delhi, KCL, Illinois, and Harvard Law School.
- Global Network: Connect with professionals across medical, legal, academic, and policy domains.
- Convenient Learning: Ten sessions, Thursday afternoons (CET), fully online. Mark your calendar from September 2024 to November 2024.
Ready to lead at the forefront of health and life science innovation law? Join us!
The Inter-CeBIL Master Class consists of ten sessions which will run on Thursday afternoons (with one Friday and one Wednesday session) CET between 14:00-16:30, from September 2024 through November 2024. The course is fully online and consists of a series of live lectures, case studies, and interactive discussions led by world-leading experts.
For questions, contact Sebastian Porsdam Mann: Sebastian.porsdam.mann@jur.ku.dk
Course directors
Course details
Kick-off – an overview of the regulatory landscape for bioscience innovation
The course kick-off will be led by Prof. Timo Minssen, Director of CeBIL and PI of the Inter-CeBIL programme, who will provide a brief overview of the Inter-CeBIL program and its studies, followed by two lectures on:
- Regulating medical AI and machine learning in Europe: Core legal and ethical aspects of an evolving eco-system
- Navigating the EU AI Act and its’ interface with the Medical Device Regulation (MDR): Implications for Regulated Digital Medical Products
Introductory session 2.5 hours (3 credits)
Time: 6 September 2024, 14:00 CET
Module 1: Frontiers in Medical Technology
This module provides an in-depth exploration of the legal and regulatory implications of emerging technologies transforming healthcare, such as AI, blockchain, and quantum computing. Participants will examine the EU AI Act and its potential impact on the development and deployment of AI-powered medical devices, as well as the challenges and opportunities presented by quantum computing for drug discovery and personalized medicine.
Instructors:
- Professor I. Glenn Cohen, Deputy Dean, Harvard Law School
- Professor Ole Lund, Department of Health Technology, Technical University of Denmark
- Associate Professor Sara Gerke, University of Illinois Law School
Module length: 3 x 2.5 hours (9 credits)
Time: 12, 19, 26 September 2024, 14:00 CET
Instructor | Date | Time |
---|---|---|
Gerke | 12 September | 14:00 |
Cohen | 19 September | 14:00 |
Lund | 26 September | 14:00 |
Module 2: Regulation, Facilitation, & Innovation
This module focuses on strategies for facilitating scientific progress through effective regulation and policy. Participants will analyze evidence-based approaches to intellectual property policy, incentives for research and development, and legal frameworks for drug repurposing. The module will also cover the lessons learned from the COVID-19 pandemic and the need for proactive and coordinated approaches to pandemic preparedness.
Instructors:
- Professor Kathleen Liddell, Director, Centre for Law, Medicine and Life Sciences, University of Cambridge
- Professor Jacob S. Sherkow, University of Illinois Colleges of Law and Medicine
- Dr. John Liddicoat, Senior Lecturer, King’s College London Dickson Poon School of Law
Module length: 3 x 2.5 hours (9 credits)
Time: 03, 09, 17 October 2024, 1400 CET
Instructor | Date | Time |
---|---|---|
Sherkow | 03 October | 14:00 |
Liddicoat | 09 October | 14:00 |
Liddell | 17 October | 14:00 |
Module 3: Ethical, Sustainable, and Responsible Innovation
The final module addresses the legal and ethical dimensions of promoting sustainable, responsible, and equitable biomedical innovation. Participants will examine strategies for increasing diversity and inclusion in clinical trials, mitigating biases and discrimination in medical AI, and aligning innovation with societal values and environmental sustainability. The module will also cover the role of patient and public involvement in shaping the direction of biomedical research and innovation.
Instructors:
- Susannah Baruch, Executive Director, Petrie-Flom Center, Harvard Law School
- Dr. Kshitij Kumar Singh, Faculty of Law, University of Delhi
- Associate Professor Jakob Wested, Faculty of Law, University of Copenhagen
Module length: 3 x 2.5 hours (9 credits)
Time: 24, 31 October, 7 November 2024, 14:00 CET
Note that the final speaker 7 November, Susannah Baruch, has not yet confirmed this date.
Instructor | Date | Time |
---|---|---|
Wested | 24 October | 14:00 |
Singh | 31 October | 14:00 |
Baruch? | 07 November | 14:00 |
Throughout the Master Class, participants will have the opportunity to engage in live Q&A discussions with the instructors and to network with their peers from diverse professional backgrounds.
More info
Language: English
Format: Online
Certificate of participation:
A certificate of attendance for 30 lessons/credits will be issued after the Master Class based on documented participation. The course has been approved in advance by the Danish Bar Association (Advokatsamfundet) as generally relevant for lawyers, cf. the executive order on ongoing mandatory continuing education for lawyers and trainee attorneys § 2.
Understand Emerging Technologies: Grasp the basic concepts and advancements in healthcare technologies.
Navigate Regulatory Challenges: Describe the fundamental regulatory, legal, and ethical issues related to digital health.
Assess Data Sharing: Identify new opportunities and risks associated with data sharing from various disciplinary perspectives, with a focus on privacy and data protection.
Apply Interdisciplinary Approaches: Explain how interdisciplinary strategies can address problems at the intersection of law and technology.
The Inter-CeBIL Master Class is designed for legal, medical, scientific, and policy professionals who wish to deepen their understanding of the legal and regulatory challenges and opportunities presented by cutting-edge developments in biomedical innovation. The course is particularly relevant for:
- Lawyers and legal professionals advising clients in the life sciences and technology sectors.
- Policymakers and regulators involved in shaping the legal and regulatory framework for bioscience innovation.
- Medical and scientific professionals involved in research and development of new technologies and therapies.
- Executives and entrepreneurs in the biomedical and technology industries
- Patient advocates and representatives from civil society organizations.
A certificate of attendance for 30 lessons/credits will be issued after the Master Class based on documented participation. The course has been approved in advance by the Danish Bar Association (Advokatsamfundet) as generally relevant for lawyers, cf. the executive order on ongoing mandatory continuing education for lawyers and trainee attorneys § 2.
Based on a generous grant from Novo Nordisk Foundation, the course will be tuition-free.
Don't miss this opportunity to learn from and network with leading experts at the forefront of bioscience innovation law!
To register, please use this registration form no later than 5 September 23:59 CET
Location
Faculty of Law
University of Copenhagen
South Campus, Faculty of Law
Njalsgade 76
DK-2300 København S
Denmark
Contact
Faculty of Law
evu@jur.ku.dk
+45 35 32 35 10
Questions about the course content should
be directed to Sebastian Porsdam Mann
E-mail: sebastian.porsdam.mann@jur.ku.dk