(MENAFN- GlobeNewsWire - Nasdaq) The Veterinary API Manufacturing market presents opportunities in expanding companion animal care, demand for livestock disease management, and enhanced regulatory compliance. Growth is driven by advancements in process technology, strategic outsourcing, and rising global animal protein demand, focusing on supply chain resilience and regional production.Dublin, Aug. 12, 2025 (GLOBE NEWSWIRE) -- The "Veterinary Active Pharmaceutical Ingredients Manufacturing - Global Strategic Business Report" report has been added to ResearchAndMarkets.com's offering.
The global market for Veterinary Active Pharmaceutical Ingredients Manufacturing was estimated at US$8.7 Billion in 2024 and is projected to reach US$12.5 Billion by 2030, growing at a CAGR of 6.3% from 2024 to 2030. This comprehensive report provides an in-depth analysis of market trends, drivers, and forecasts, helping you make informed business decisions.
What Factors Are Supporting Growth in Veterinary API Manufacturing Globally?
Growth in the veterinary active pharmaceutical ingredients manufacturing market is driven by several factors related to rising demand for animal protein, increased companion animal care, and stricter disease management protocols. Expansion of commercial livestock farming and aquaculture is driving volume demand for antiparasitics, antibiotics, and nutritional APIs. Growth in pet ownership and veterinary clinics in both developed and emerging regions is supporting small-batch production of APIs for dermatological, cardiovascular, and endocrine therapies.
Regulatory mandates for controlled antimicrobial use are prompting reformulation efforts and development of narrow-spectrum APIs. Investments in regional API production hubs, particularly in Asia and Latin America, are improving supply chain stability and cost efficiency. Strategic outsourcing and technological modernization in synthesis, purification, and process validation are further enhancing the capacity and compliance of veterinary API manufacturing facilities worldwide.
Why Is Veterinary API Manufacturing Central to Animal Health Supply Chains?
Veterinary active pharmaceutical ingredients (APIs) are the core biologically active substances used to formulate medications for animals. These APIs form the basis of drugs used for disease prevention, treatment, and performance enhancement in livestock, companion animals, and aquatic species. Veterinary API manufacturing supports a wide spectrum of products, including antibiotics, anti-parasitics, anti-inflammatories, and vaccines. The manufacturing process involves synthesis, fermentation, purification, and formulation of APIs that meet regulatory quality standards for animal use.
Manufacturing of veterinary APIs must adhere to specific pharma-copoeial guidelines and good manufacturing practices (GMP), with added emphasis on contamination control and species-specific efficacy. As animal health becomes closely tied to food safety, public health, and economic productivity, secure and consistent API supply is essential for the continuity of veterinary healthcare systems. This has heightened the focus on supply chain resilience, particularly for high-volume livestock drugs used in poultry, swine, and bovine segments.
How Are Regulatory Shifts and Global Trade Influencing API Production?
Veterinary API manufacturing is shaped by evolving regulatory frameworks focused on drug residue limits, antimicrobial stewardship, and export quality compliance. Many regions now require traceability and transparent documentation of the origin and composition of veterinary drugs. This has increased scrutiny on API manufacturers and driven demand for production facilities that comply with veterinary GMP standards, such as those issued by the FDA, EMA, and national veterinary authorities.
International trade of veterinary APIs is also affected by harmonization initiatives, such as VICH guidelines and Codex Alimentarius standards. These influence residue monitoring programs and acceptable daily intake limits for veterinary drugs in animal-derived food products. Manufacturers must navigate differing approval pathways for veterinary APIs across regions, often requiring customized production and documentation for each export destination. These compliance requirements are prompting both large and mid-sized API producers to expand certifications, improve audit readiness, and invest in region-specific regulatory expertise.
What Role Do Process Technologies and Outsourcing Models Play in Manufacturing Strategy?
Advancements in synthesis, fermentation, and downstream processing technologies are enabling greater control over purity, yield, and production cost. Manufacturers are increasingly adopting continuous processing and modular production systems to improve throughput and reduce contamination risks. Microbial and enzymatic synthesis methods are being applied to veterinary hormone and vitamin APIs, while complex molecules such as antiparasitic agents require highly controlled chemical synthesis workflows.
Contract manufacturing organizations (CMOs) and contract development and manufacturing organizations (CDMOs) are playing a larger role in veterinary API supply chains. Many animal health companies outsource API production to dedicated third-party producers who specialize in veterinary-grade materials. This model supports scalability, cost optimization, and regulatory compliance while allowing drug developers to focus on formulation and distribution. As veterinary pharmaceutical pipelines diversify into biologics, CMOs with biologics capabilities are becoming integral partners in active ingredient development.
Report Features:
Comprehensive Market Data: Independent analysis of annual sales and market forecasts in US$ Million from 2024 to 2030. In-Depth Regional Analysis: Detailed insights into key markets, including the U.S., China, Japan, Canada, Europe, Asia-Pacific, Latin America, Middle East, and Africa. Company Profiles: Coverage of players such as Alivira Animal Health Limited, AMGIS Lifescience Ltd, Ceva Sante Animale S.A., Chempro Pharma Private Limited, Divi`s Laboratories Limited and more. Complimentary Updates: Receive free report updates for one year to keep you informed of the latest market developments.
Key Insights:
Market Growth: Understand the significant growth trajectory of the In House Service segment, which is expected to reach US$9.3 Billion by 030 with a CAGR of a 7.1%. The Contract Outsourcing Service segment is also set to grow at 4.0% CAGR over the analysis period. Regional Analysis: Gain insights into the U.S. market, estimated at $2.4 Billion in 2024, and China, forecasted to grow at an impressive 10.0% CAGR to reach $2.6 Billion by 2030. Discover growth trends in other key regions, including Japan, Canada, Germany, and the Asia-Pacific.
Scope of Study:
Service (In House Service, Contract Outsourcing Service) Synthesis Type (Chemical-based API Synthesis, Biological API Synthesis, HPAPI Synthesis) Animal Type (Production Animals, Companion Animals) Therapeutic Category (Antiparasitic Therapeutic, Anti-infectives Therapeutic, NSAIDs Therapeutic, Other Therapeutic Categories)
Key Attributes:
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