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Table of Contents
    Workshop Registration End Date :2025-05-20

    Virtual Workshop

    Bioethics and Legal Regulation of Human Enhancement Technologies

    MODE
    Virtual / Online
    TYPE
    Mentor Based
    LEVEL
    Advanced
    DURATION
    3 Days
    START DATE
    20 -May -2025
    TIME
    1:00 PM IST

    About

    As technology reshapes the boundaries of human capabilities, ethical and legal regulation becomes pivotal. This intensive 3-days workshop delves into the scientific basis of HETs, explores key ethical principles, examines global legal standards, and studies real-world case precedents. Participants will critically engage with regulatory challenges and craft forward-looking policy approaches to emerging bio-enhancement technologies, fostering a nuanced global perspective.

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    Workshop Objectives

    • To introduce the fundamental science behind human enhancement technologies such as CRISPR and neural interfaces.

    • To examine the core bioethical principles and their application in regulating human enhancement.

    • To explore national and international legal instruments governing human enhancement technologies.

    • To discuss landmark cases and regulatory challenges across different jurisdictions.

    • To encourage cross-cultural understanding of ethical debates on biotechnology.

    • To prepare participants to anticipate and engage with the future regulatory needs of emerging biotechnologies.

    Workshop Structure

    Day 1: Foundations pf HETs – Science, Ethics & Global Perspectives

    ● CRISPR, neuro enhancement, and ethical limits under international biomedical law.
    ● Understanding Human Enhancement Technologies Introduction to CRISPR gene editing, brain-computer interfaces, and neural implants
    ● Therapy vs. Enhancement: Drawing the Ethical Line Examining concepts like medical necessity, human dignity, and the transhumanist debate
    ● Core Bioethics Principles in Practice Autonomy, beneficence, non-maleficence, and justice in the context of biotechnology
    ● Cross-Cultural and Religious Perspectives Comparative insights into how diverse ethical systems interpret enhancement technologies

    Day 2: Regulation in Action – Law, Oversight & Global Standards

    ● Global Bio-Legal Instruments UNESCO Declaration, WHO ethics guidance, and the Oviedo Convention
    ● Comparative National Regulations Case studies from the EU, USA, India, China, and Brazil
    ● Governing CRISPR and Genetic Editing Discussion of moratoriums, oversight mechanisms, and permissible practices
    ● Regulating Neuro enhancement and Brain Technologies Brain privacy, cognitive liberty, and informed consent in neurotech

    Day 3: Case Studies, Risks & the Future of Policy Design

    ● Legal Precedents & Landmark Cases Disputes and litigation in human enhancement across jurisdictions
    ● Risk Governance in Emerging Tech Applying the precautionary principle, public trust, and regulatory accountability
    ● The Path Toward Global Harmonization Discussion on treaties, conventions, and cross-border regulatory cooperation
    ● Ethical Futures and Policy Innovation Roundtable on what should be regulated, how, and why

    Intended For

    • Law students, scholars, and practitioners specializing in health law, technology law, and bioethics

    • Biotechnology researchers and professionals

    • Medical professionals interested in ethical aspects of biotechnology

    • Policymakers, regulatory professionals, and think tanks

    • Graduate and postgraduate students from life sciences, legal studies, public policy, and allied fields

    • Anyone interested in the intersection of science, ethics, and global governance

    Important Dates

    Registration Ends

    2025-05-20
    Indian Standard Timing 11:00 AM

    Workshop Dates

    2025-05-20 to 2025-05-22
    Indian Standard Timing 1:00 PM

    Workshop Outcomes

    • Critically analyze the ethical implications of emerging human enhancement technologies.

    • Interpret and compare international bio-legal frameworks and conventions.

    • Apply bioethical principles to real-world scenarios involving human enhancement.

    • Evaluate the governance models and risk management strategies for biotechnology innovations.

    • Design policy proposals aimed at harmonizing regulation of HETs across jurisdictions.

    Mentor Profile

    Pulidindi passport 13.11.2018 0000

    Mr. Indra Neel Pulidindi

    Scientific consultant

    Jesus’ Scientific Consultancy for Industrial and Academic Research (JSCIAR)

    more

    Fee Structure

    Student

    INR. 1999
    USD. 50

    Ph.D. Scholar / Researcher

    INR. 2999
    USD. 60

    Academician / Faculty

    INR. 3999
    USD. 70

    Industry Professional

    INR. 5999
    USD. 95

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    Key Takeaways

    • Access to Live Lectures
    • Access to Recorded Sessions
    • e-Certificate
    • Query Solving Post Workshop
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