India-UK Trade Agreement Raises Concerns
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Article Summary
The article elaborates on the implications of the India-United Kingdom Comprehensive Economic and Trade Agreement (CETA), specifically focusing on the provisions related to intellectual property, particularly concerning access to affordable medicines through licensing mechanisms. Here is a detailed summary:
Summary:
CETA Overview:
- The India-UK CETA has raised concerns over India's commitments, especially in Chapter 13, which addresses intellectual property.
- Article 13.6 specifically emphasizes the preference for voluntary licensing over compulsory licensing for ensuring access to medicines.
Compulsory vs. Voluntary Licensing:
- India traditionally advocated for compulsory licensing to combat high prices of patented medicines, allowing local production to improve affordability.
- A significant case was the 2012 grant of compulsory license to Natco Pharma for sorafenib tosylate, which reduced treatment costs from ₹2,80,428 to ₹8,800.
Legislative Background:
- India's Patents Act was amended to align with the WTO TRIPS Agreement, which permits compulsory licensing after three years from the patent grant.
- The legislation allows compulsory licenses if the patented invention is either not satisfying reasonable public requirements or not available at affordable prices in India.
Impact of CETA:
- India's commitment to voluntary licensing as per CETA would undermine its longstanding position advocating for compulsory licensing in international forums.
- This shift weakens a key provision of the 2001 Doha Declaration, which allows member countries to issue compulsory licenses amid public health crises.
Concerns with Voluntary Licensing:
- Critics argue that voluntary licensing does not adequately ensure affordable access to medicines, citing the weak negotiating power of domestic companies against multinational pharmaceutical firms.
- The experience with Cipla's remdesivir, produced under a voluntary license from Gilead Sciences, showed pricing higher than that set by Gilead in the U.S., highlighting the limitations of voluntary arrangements.
Technology Transfer Issues:
- CETA's provisions may compromise India's demand for technology transfer on favorable terms, a demand reiterated in various multilateral discussions, including the UN's NIEO resolution (1974), aimed at facilitating technology sharing with developing nations for industrialization.
- India's Fourth Biennial Update Report to the UNFCCC (2024) noted that barriers such as slow technology transfer and stringent IPR impede the adoption of climate-friendly technologies.
Constitutional and International Implications:
- The change in stance might affect India's leverage in future negotiations regarding technology transfer essential for tackling climate change and promoting industrial development.
- The article emphasizes the need for India to reassess its position on compulsory licensing to ensure health security and sustainable technological advancements.
Key Points:
- The India-UK CETA impacts India's position on intellectual property, particularly concerning medicines access.
- Voluntary licensing is favored in CETA, opposing India's historical support for compulsory licensing.
- Compulsory licensing was pivotal in reducing medicine prices significantly in the past.
- The Doha Declaration reaffirms the right to issue compulsory licenses, a stance India now weakens by conceding to voluntary licensing.
- Concerns about the effectiveness of voluntary licensing highlighted by price disparities in past cases.
- Technology transfer issues related to climate change and industrialization are at risk due to concessions made in CETA.
- India's demands for favorable terms in technology transfer could be adversely affected, impacting its developmental strategies.
The article indicates the necessity for India to strike a balance between complying with international trade agreements while safeguarding public health interests and advancing its industrial capabilities.
Key Terms & Concepts
| India-United Kingdom Comprehensive Economic and Trade Agreement | Main focus of the article |
| TRIPS | Intellectual property framework |
| compulsory licensing | Key safeguard for access |
| World Trade Organization | Regulatory body |
| Patents Act | Legislation on patents |
| Médecins Sans Frontières | Critique on licensing terms |
| Gilead Sciences | Patent holder of remdesivir |
| Fourth Biennial Update Report | Report on technology transfer |
| United Nations | International organization |
| climate change | Subject of international concern |




