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Bora Pharmaceuticals (6472) investor relations material
Bora Pharmaceuticals 44th Annual J.P. Morgan Healthcare Conference summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Strategic growth and global expansion
Achieved 700% market cap growth since 2017, surpassing $2 billion, through organic growth and strategic acquisitions, including Upsher-Smith, Pyros, Emergent's sterile fill and finish facility, and Tanvex, expanding U.S. and biologics capabilities.
Operates 10 manufacturing sites (5 in North America, 5 in Taiwan), exporting to 100+ countries, with 95% of revenue from outside Taiwan and a strong focus on North America.
Became the first Taiwanese company to join the U.S. OTCQX market, enhancing global visibility and investor access, with cross-market trading starting in 2026.
Re-signed multi-year commercial contracts, including a $350 million deal, and made record CapEx and sales/marketing investments in 2025.
Integrated Tanvex BioPharm as Bora Biologics, completing full-service CDMO capabilities in both small and large molecules and entering the large molecule sector.
Operational and financial performance
Fiscal 2025 revenue reached $634 million, with 3Q25 revenue at $195 million; net income from continuing operations was $129 million.
CDMO business grew 53.8% year-over-year to over $340 million, with a 96% OTIF rate and improved efficiency.
EBITDA margin rose to 40% in 2024 from 17% in 2017, with steady ROIC expansion and a focus on value creation.
Discontinued nonprofitable operations, reducing net working capital utilization from 53% to 23.69% and freeing up capital for investment.
Maintained strong cash positions, increased CapEx, paid dividends, and kept a consistent debt-to-EBITDA ratio.
Investments and capacity enhancements
Invested $400 million in U.S. CapEx over two years, focusing on organic growth, integration post-acquisition, and major investments in aseptic technologies and new filling lines across US, Canada, and Taiwan.
Maryland site received a city lab permit in Dec. 2025; cleanroom construction and validation batches scheduled for 2026.
Canadian facility increased derma product capacity by 40%, supporting a dermatology market projected to double by 2030.
New liquid-filled hard capsule capability in Taiwan to be operational in 1Q26, targeting oncology and potent drugs.
Expanded aseptic fill and finish and biologics capabilities in the U.S., with new lines and technologies coming online in 2025–2026.
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