+353-1-416-8900REST OF WORLD
+44-20-3973-8888REST OF WORLD
1-917-300-0470EAST COAST U.S
1-800-526-8630U.S. (TOLL FREE)
Sale

Oral Solid Dosage Contract Manufacturing Market - Global Forecast 2025-2032

  • PDF Icon

    Report

  • 199 Pages
  • November 2025
  • Region: Global
  • 360iResearch™
  • ID: 5666205
UP TO OFF until Jan 01st 2026
1h Free Analyst Time
1h Free Analyst Time

Speak directly to the analyst to clarify any post sales queries you may have.

Senior executives face a demanding landscape in the oral solid dosage contract manufacturing sphere, where rapidly shifting regulations, customer requirements, and heightened compliance standards drive the need for agile business strategies and robust partnerships.

Market Snapshot: Oral Solid Dosage Contract Manufacturing Market

The oral solid dosage contract manufacturing market attained USD 44.16 billion in 2024, is forecast to expand to USD 48.20 billion in 2025, and is expected to reach USD 87.70 billion by 2032, reflecting a compound annual growth rate of 8.95%.

Growth is underpinned by the increasing need for tailored product development and accelerated launch cycles as pharmaceutical organizations race to bring new therapies to market. Dynamic collaborations between contract manufacturers and pharmaceutical companies are redefining value, streamlining launch processes, and advancing global expansion through technology-driven manufacturing and continuous improvement initiatives.

Scope & Segmentation of the Oral Solid Dosage Contract Manufacturing Market

  • Form Types: Covers hard and soft gelatin capsules, multiparticulate products, coated and uncoated tablets, and granules. This variety supports the diverse formulation and therapeutic requirements of the industry.
  • Therapeutic Areas: Encompasses segments such as anti-infective, cardiovascular, central nervous system, oncological, and gastrointestinal. Broad therapeutic coverage enables manufacturers to engage with evolving clinical demands.
  • Applications: Includes prescription drugs and over-the-counter solutions. Providers leverage regulatory experience and coordinated logistics to facilitate global market entry and compliance.
  • Development Stages: Spans research and development through commercial-scale production, ensuring a seamless path from early formulation to market rollout.
  • Customer Types: Serves biotechnology enterprises, nutraceutical producers, and established pharmaceutical organizations, allowing for customization in service models based on shifting market focus.
  • Regional Coverage: Operations extend across the Americas, Europe, Middle East & Africa, and Asia-Pacific. Region-specific regulatory conformity and supply chain adaptability support market agility and resilience.
  • Technologies and Business Strategies: Employs automation, modular facilities, digital oversight, analytics, and sustainability programs. These assets promote transparent operations, resource efficiency, and responsive distribution networks.
  • Leading Companies: Key providers include Catalent, Thermo Fisher Scientific, Lonza Group, Recipharm, Siegfried Holding, Fareva, PCI Pharma Services, Aurobindo Pharma, Ajinomoto Bio-Pharma Services, and Piramal Pharma, each presenting broad service portfolios to address all market segments.

Key Takeaways for Senior Decision-Makers

  • Strengthen alignment with seasoned contract manufacturing organizations to stay ahead of evolving compliance mandates and facilitate timely introduction of new oral solid dosage products.
  • Adopt automated and modular production capabilities to rapidly adapt to regulatory or supply chain changes, improving organizational agility amid market uncertainty.
  • Utilize advanced supply chain analytics for more effective inventory management and uninterrupted distribution, providing a buffer against unforeseen disruptions.
  • Increase supplier collaboration to expedite problem resolution, ensuring regulatory readiness and the ability to capitalize swiftly on new business opportunities.
  • Integrate ESG-focused initiatives to ensure visibility and accountability in manufacturing and distribution, achieving key benchmarks in corporate responsibility.

Tariff Impact: Navigating the 2025 US Regulatory Shift

The coming changes to US tariff structures in 2025 are prompting contract manufacturers to evaluate procurement strategies and diversify supply chains. Organizations are prioritizing nearshoring, alternative sourcing, and investment in digital technology to enhance supply continuity and operational stability. Forming robust partnerships is proving essential for navigating the evolving regulatory and tariff landscape, increasing responsiveness to cost fluctuations, and maintaining flexibility.

Methodology & Data Sources

This analysis draws on structured executive interviews, regulatory insights, and primary market research. All findings are cross-validated with public documentation and industry disclosures, delivering timely, accurate information for senior leadership decision-making.

Why This Report Matters

  • Equips leaders with thorough segmentation and regional market perspectives, informing effective supplier selection and capital deployment in oral solid dosage contract manufacturing.
  • Delivers actionable intelligence on technology trends and risk management, highlighting operational adaptability and supply chain resilience as central to market success.
  • Informs confident, evidence-based strategic choices that align with regulatory, technological, and global market developments.

Conclusion

By closely tracking trends in oral solid dosage contract manufacturing, business leaders can fine-tune strategies, drive operational efficiency, and maintain readiness for ongoing sector evolution.

 

Additional Product Information:

  • Purchase of this report includes 1 year online access with quarterly updates.
  • This report can be updated on request. Please contact our Customer Experience team using the Ask a Question widget on our website.

Table of Contents

1. Preface
1.1. Objectives of the Study
1.2. Market Segmentation & Coverage
1.3. Years Considered for the Study
1.4. Currency & Pricing
1.5. Language
1.6. Stakeholders
2. Research Methodology
3. Executive Summary
4. Market Overview
5. Market Insights
5.1. Adoption of continuous manufacturing technologies to accelerate oral solid dosage production and reduce batch variability
5.2. Implementation of advanced digital twins and real-time PAT monitoring in contract manufacturing facilities for improved quality control
5.3. Surge in specialty modified-release and targeted oral solid dosage formulations to meet personalized medicine demands
5.4. Expansion of high-potency active pharmaceutical ingredient handling capabilities in outsourcing facilities to address oncology therapies
5.5. Integration of green chemistry principles and sustainable excipient sourcing in oral solid dosage manufacturing operations
5.6. Strategic alliances between pharma innovators and CMOs for co-development and tech transfer of complex OSD formulations
5.7. Regulatory emphasis on serialization and track-and-trace compliance driving investment in smart packaging solutions
5.8. Growth of automated end-to-end continuous granulation and tableting systems to enhance production efficiency
5.9. Rising demand for pediatric and orphan drug oral solid formulations prompting specialized contract manufacturing services
5.10. Investments in digital supply chain resilience and alternative sourcing to mitigate post-pandemic oral solid dosage disruptions
6. Cumulative Impact of United States Tariffs 2025
7. Cumulative Impact of Artificial Intelligence 2025
8. Oral Solid Dosage Contract Manufacturing Market, by Form Type
8.1. Capsules
8.1.1. Hard Gelatin
8.1.2. Soft Gelatin
8.2. Granules
8.2.1. Immediate Release
8.2.2. Modified Release
8.3. Pellets
8.3.1. Coated Pellets
8.3.2. Multiparticulate
8.4. Tablets
8.4.1. Coated
8.4.2. Uncoated
9. Oral Solid Dosage Contract Manufacturing Market, by Therapeutic Area
9.1. Anti Infectives
9.1.1. Antibiotics
9.1.2. Antivirals
9.2. Cardiovascular
9.2.1. Hyperlipidemia
9.2.2. Hypertension
9.3. Central Nervous System
9.3.1. Depression
9.3.2. Epilepsy
9.4. Gastrointestinal
9.4.1. Acid Reducers
9.4.2. Prokinetics
9.5. Oncology
9.5.1. Hematological
9.5.2. Solid Tumor
10. Oral Solid Dosage Contract Manufacturing Market, by Application
10.1. Over The Counter
10.2. Prescription Drugs
11. Oral Solid Dosage Contract Manufacturing Market, by Stage
11.1. Clinical Trial
11.2. Commercial
12. Oral Solid Dosage Contract Manufacturing Market, by Customer Type
12.1. Biotechnology
12.2. Nutraceutical
12.3. Pharmaceutical
13. Oral Solid Dosage Contract Manufacturing Market, by Region
13.1. Americas
13.1.1. North America
13.1.2. Latin America
13.2. Europe, Middle East & Africa
13.2.1. Europe
13.2.2. Middle East
13.2.3. Africa
13.3. Asia-Pacific
14. Oral Solid Dosage Contract Manufacturing Market, by Group
14.1. ASEAN
14.2. GCC
14.3. European Union
14.4. BRICS
14.5. G7
14.6. NATO
15. Oral Solid Dosage Contract Manufacturing Market, by Country
15.1. United States
15.2. Canada
15.3. Mexico
15.4. Brazil
15.5. United Kingdom
15.6. Germany
15.7. France
15.8. Russia
15.9. Italy
15.10. Spain
15.11. China
15.12. India
15.13. Japan
15.14. Australia
15.15. South Korea
16. Competitive Landscape
16.1. Market Share Analysis, 2024
16.2. FPNV Positioning Matrix, 2024
16.3. Competitive Analysis
16.3.1. Catalent, Inc.
16.3.2. Thermo Fisher Scientific Inc.
16.3.3. Lonza Group AG
16.3.4. Recipharm AB
16.3.5. Siegfried Holding AG
16.3.6. Fareva SA
16.3.7. PCI Pharma Services, Inc.
16.3.8. Aurobindo Pharma Limited
16.3.9. Ajinomoto Bio-Pharma Services, LLC
16.3.10. Piramal Pharma Limited

Companies Mentioned

The companies profiled in this Oral Solid Dosage Contract Manufacturing market report include:
  • Catalent, Inc.
  • Thermo Fisher Scientific Inc.
  • Lonza Group AG
  • Recipharm AB
  • Siegfried Holding AG
  • Fareva SA
  • PCI Pharma Services, Inc.
  • Aurobindo Pharma Limited
  • Ajinomoto Bio-Pharma Services, LLC
  • Piramal Pharma Limited

Table Information