Union Minister for Commerce and Industry, Piyush Goyal, called upon the pharmaceutical sector to take advantage of the recently launched Anusandhan National Research Foundation (ANRF) fund to drive innovation and research while speaking at the 63rd Annual Day Celebrations of the Indian Drug Manufacturers' Association (IDMA) in Mumbai themed Innovating Today For Healthier Tomorrow, Union Minister of Commerce and Industry Piyush Goyal on February 8, 2025. Addressing industry leaders, Goyal emphasized that the Rs. 50,000-crore initiative, backed by Prime Minister Narendra Modi, aims to strengthen collaboration between research institutions, academia, and the private sector.
“The
Anusandhan National Research Foundation is a revolutionary step towards making
India a global hub for research and development. I urge the pharmaceutical
industry to actively participate in this initiative and harness its potential
to bring cutting-edge innovations to the market,” Goyal stated.
The
ANRF, established under the ANRF Act 2023, seeks to foster a robust culture of
research and innovation across the country. By investing in ANRF and promoting
private sector involvement, the government aims to boost India’s position in
global innovation rankings and ensure that research translates into economic
and societal benefits. The recently presented Union Budget 2024-25 underscores
the government’s commitment to advancing scientific endeavors, with significant
allocations to the space economy, agricultural research, and nuclear
advancements.
Minister
of State for Commerce and Industry, Anupriya Patel, highlighted the
significance of the foundation in enhancing India’s research landscape. “By
empowering early career researchers and providing necessary resources, we are
building a strong pipeline of innovation that will benefit industries like
pharmaceuticals, biotechnology, and healthcare,” she remarked.
Dr.
Rajeev Singh Raghuvanshi, the Drugs Controller General of India (DCGI), echoed
these sentiments, emphasizing the importance of the pharmaceutical industry's
participation in research initiatives. “India’s pharmaceutical sector has
always been at the forefront of global healthcare solutions,” he noted.
He
further added, “There is a need for focused interventions in areas like
dissolution, assay content, microbial control to improve drug quality.
The
Prime Minister’s Early Career Research Grant, a flagship initiative under ANRF,
offers up to Rs. 60 lakh plus overheads over three years to support emerging
researchers. The program provides flexibility in resource allocation, manpower
recruitment, and travel allowances, including international travel for
project-related activities. A maximum of 700 grants will be awarded annually
across various subject areas, ensuring a steady influx of research-driven
advancements.
Goyal
emphasized that the ease of doing research measures introduced under ANRF, such
as enhanced funding for open access publications, patent filings, and
contingency support, will significantly benefit industries reliant on
innovation. “With these strategic initiatives, we are creating an ecosystem
that fosters ground-breaking research, accelerates scientific advancements, and
positions India as a leader in global R&D,” he added.
With
the launch of ANRF, India is set to make significant strides in research and
innovation, paving the way for transformative discoveries and strengthening its
position in the global knowledge economy.
“Our
members have successfully ensured that India continues to have the largest
number of WHO Prequalified Finished Pharmaceutical Products Manufacturers under
various medical verticals and is also rated the largest supplier country of
generic drugs by UNICEF,” informed Dr. Viranchi Shah, national president, IDMA.
Daara
Patel, secretary general of IDMA convened the proceedings of the Annual Day
Celebration.
The
Indian pharmaceutical market will reach US$ 65 billion by 2024 and further
expand to reach US$ 120-130 billion by 2030. IDMA Members' Export Record
approximately 75% in formulations and 85% in APIs. India thus has maintained
its global regulatory approval dominance with 700 US FDA Sites. Highest in any
country outside the US, 650 EU GMP certified sites and 1800+ WHO GMP certified
units.
“Timely
and effective representations to Government authorities for quick resolutions
of issues and quick response to Members' queries are one of our main
strengths,” Dr. Shah added.
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