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Research Paper Volume 6 Issue 4 333 - 345 August 11, 2024

Comparative Analysis of Gene Editing and Patenting Laws: India vs. EU

Lead author · Corresponding
Archana Viswanath
Pursued LL.M. from Queen Mary University of London
Abstract

This paper provides a comparative analysis of the legal and ethical frameworks governing gene editing and patenting in India and the European Union (EU). Both regions welcome advancements in gene editing but impose stringent restrictions to maintain ethical compliance and public safety. The Indian Patent Act, with Sections 3(b), 3(c), and 3(j), and the EU's morality and ordre public doctrines limit the patentability of genetic modifications. While India permits gene editing in plant biotechnology, biomedical research faces tighter regulations under the Indian Council of Medical Research (ICMR) and the Department of Biotechnology (DBT). Similarly, the EU's regulatory bodies maintain strict oversight to prevent unethical practices. This paper discusses the evolving guidelines, including India's 2020 draft by DBT and CDSCO, and the EU's established frameworks, highlighting their approaches to balancing innovation and ethical integrity. By comparing these regulations, the paper elucidates how both regions navigate the complexities of gene editing to foster advancements while safeguarding societal values.

Type
Research Paper
Information
International Journal of Legal Science and Innovation, Volume 6, Issue 4, Page 333 - 345
Creative Commons
CC BY-NC 4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution–NonCommercial 4.0 International (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/), which permits remixing, adapting, and building upon the work for non-commercial use, provided the original work is properly cited.
Copyright
Copyright © IJLSI 2026
Disclaimer
The views and opinions expressed in this manuscript are those of the author(s) alone and do not reflect the views, policies, or position of the Journal.

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