ENVALITH
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KOA SHOJI HOLDINGS CO.,LTD.

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コーア商事ホールディングス株式会社 logo
KOA SHOJI HOLDINGS CO.,LTD.9273

Business

Koa Shoji Holdings is a pharmaceutical group comprising three consolidated subsidiaries under a holding company structure. It consists of two segments: the API Sales Business, in which Koa Shoji Co., Ltd. imports active pharmaceutical ingredients (APIs) from more than 90 overseas suppliers across 10 countries worldwide and supplies them to over 100 domestic pharmaceutical companies; and the Pharmaceutical Manufacturing and Sales Business, in which Koa Isei Co., Ltd. and Koa Biotech Bay Co., Ltd. manufacture and sell injectable formulations—centered on Prefilled Syringe Formulations—both in-house and on a contract manufacturing basis. Benefiting from the national policy tailwind of expanding generic drug adoption, the group has built an integrated supply system spanning stable API procurement through to formulation manufacturing. Its main customers are domestic generic drug manufacturers, with its largest customer, Fuso Pharmaceutical Industries, Ltd., accounting for 21.6% of sales.

Business Model

In the API Sales Business, the company adds quality assurance—provided by its in-house analysis functions (such as the Osaka Pharmaceutical Analysis Center)—to APIs imported from overseas suppliers, then sells them to domestic pharmaceutical companies, earning a trading margin. In the Pharmaceutical Manufacturing and Sales Business, in addition to manufacturing and selling its own in-house developed generic drugs, the company undertakes contract manufacturing (CMO/CDMO) for major domestic manufacturers, earning a manufacturing margin. Through group synergies between the two businesses, the company maintains a system capable of providing integrated value, from API procurement through to formulation manufacturing.

Company Strengths

Koa Shoji Co., Ltd. has built trading relationships with over 90 overseas suppliers in 10 countries worldwide since its founding. It has achieved stable procurement and price competitiveness through a multi-supplier purchasing system, and maintains a supply base covering over 100 domestic pharmaceutical companies. Its ownership of in-house analytical functions (such as the Osaka Pharmaceutical Analysis Center) allows it to internalize quality assurance functions despite being a trading company, which serves as a differentiating factor.

Koa Isei Co., Ltd. newly established the Zao Plant in 2016, possessing advanced containment facilities specialized in the manufacture of highly pharmacologically active injectable drugs such as anticancer agents. It has manufacturing capability for Prefilled Syringe Formulations, and achieved a segment profit margin of 24.7% in the Pharmaceutical Manufacturing and Sales Business for FY2025 (ended June 2025). High technology and capital investment barriers function as a barrier to entry.

Revenue grew for 5 consecutive periods, from ¥17,816 million in FY2021 (ended June 2021) to ¥23,269 million in FY2025 (ended June 2025). Operating profit expanded from ¥3,377 million to ¥5,355 million over the same period. As of the end of FY2025 (ended June 2025), the equity ratio stood at 77.9% and cash and cash equivalents totaled ¥14,739 million, indicating high financial soundness, with the financial capacity to fund the approximately ¥6,500 million investment in the Zao Second Plant through internal funds and borrowings.

ENVALITH's Perspective

The cumulative revenue growth rate of 4.0% and operating profit growth rate of 4.5% for the nine months ended March 2026 (3Q FY2026) represent a significant slowdown from the same period a year earlier (revenue up 5.1%, operating profit up 22.8%). Segment profit in the Pharmaceutical Manufacturing and Sales Business turned flat, down 0.1% year on year, reflecting the impact of competitive entry into mainstay Tablets and Other Formulations. While the impact of the March 2026 drug price revision (average deviation rate of 4.8%) as an external factor was relatively contained, ongoing attention is needed regarding how future drug pricing system changes (such as the shortened G1 rule and changes to authorized generic drug pricing) will affect the medium-term earnings structure.

Construction of the second Zao plant is proceeding on schedule, targeting completion in June 2026 and operational startup in July 2027, with construction in progress increasing by ¥1,476 million from the end of the previous fiscal year to reach ¥4,716 million. Whether the increased production capacity after startup translates into expanded CDMO orders and increased supply of highly potent injectable formulations will be key to medium-term performance. At the same time, there is a risk that fixed cost increases and startup costs incurred before operations begin could temporarily weigh on profits, requiring careful assessment of earnings trends for FY2027 (ending March 2027).

In the cumulative nine months of the current fiscal year, a foreign exchange loss of ¥55,007 thousand was recorded, a significant deterioration from the foreign exchange gain of ¥17,098 thousand in the same period a year earlier. Given the business characteristic of relying heavily on imported active pharmaceutical ingredients, a weaker yen directly pressures earnings through higher procurement prices. While exchange rate fluctuations are an uncontrollable external factor, the company has implemented measures such as forward contracts, price negotiations with overseas suppliers, exchange-rate-linked pricing, and the introduction of foreign-currency-denominated amortizing bonds. The effectiveness of these hedging measures and the company's ability to pass on procurement cost increases amid a continued weak yen will be the focal points for maintaining profit margins going forward.

Growth Strategy

Aiming for FY2030 net sales of ¥40.0 billion and operating profit of ¥8.0 billion, the company is advancing its transformation into a specialized pharmaceutical trading company and a leading domestic manufacturer of injectable formulations

The second plant under construction in Zao, Yamagata Prefecture is progressing on schedule, targeting completion in June 2026 and start of operations in July 2027. Construction in progress has reached ¥4,716 million; upon start-up, production capacity for highly potent injectable formulations, Prefilled Syringe Formulations, and other products will be substantially expanded, aiming to increase CDMO orders and sales to external customers.

In preparation for the pharmaceutical manufacturing license renewal scheduled for December 2026, the company is advancing measures to ensure pharmaceutical quality and safety and to strengthen its stable supply system. Reliable execution of the license renewal is a prerequisite for maintaining continued stable supply of existing products and preserving customer trust.

Renewal of the Yokohama Pharmaceutical Analysis Center is under consideration to address aging facilities and increasing transaction volumes. By strengthening analytical and quality evaluation functions, the company aims to enhance its proposal capabilities to pharmaceutical company customers and expand the range of new API items handled, thereby maintaining and strengthening competitive advantage in the API Sales Business.

Against the backdrop of an increase in the selected medical care burden for long-listed products (from June 2026, one-half of the price difference) and changes to the Authorized Generic (AG) drug pricing system (from October 2026), demand for generic drugs is expected to expand. Market penetration of allergy medications, central nervous system drugs, sensory organ drugs, and other products launched in recent years is progressing, leading to a continued increase in transaction volumes.

A medium-term management plan through FY2028 (ending June 2028) has been formulated to achieve the financial targets of the 2030 long-term business plan. The API Sales Business is being transformed into a "specialized pharmaceutical trading company," while the Pharmaceutical Manufacturing and Sales Business is being transformed into a "leading domestic manufacturer of distinctive injectable formulations." Full-year forecasts for FY2026 (ending June 2026) (net sales of ¥25,700 million and operating profit of ¥5,430 million) represent year-on-year increases of 10.4% and 1.4%, respectively.

Last updated: July 17, 2026