Straits Research released its highly anticipated report, “Global Regulatory Consulting Outsourcing Services Market Size & Outlook, 2026-2034. According to the study, the market size is valued at USD 2.40 billion in 2025 and is anticipated to grow till USD 4.94 billion by 2034, growing at a CAGR of 8.36% from 2026-2034.
The regulatory consulting outsourcing services market is driven by rising regulatory complexity across drugs, biologics, and medical devices, which increases documentation volume, submission frequency, and authority engagement throughout product lifecycles. Expansion of oncology and specialty therapy pipelines elevates regulatory scrutiny, accelerated review interactions, and post-approval obligations, prompting pharmaceutical and biotechnology companies to rely on external regulatory consultants for structured strategy development and submission execution. Growing participation of small and medium-sized companies in global development programs further strengthens demand for outsourced regulatory expertise, as these organizations prioritize flexible access to region-specific knowledge without expanding internal teams. However, the market faces restraint from variability in regulatory expectations across countries and regions, which complicates standardized consulting delivery and increases dependency on localized expertise. Differences in submission formats, review timelines, and data interpretation requirements create coordination challenges for consulting providers managing multi-jurisdictional programs. Additionally, sponsor concerns around data confidentiality and long-term knowledge retention limit full outsourcing of strategic regulatory functions. Despite these challenges, a strong opportunity exists in the expansion of integrated regulatory lifecycle support models that combine advisory services with submission management, regulatory intelligence, and post-approval maintenance. Consulting providers that align regulatory strategy with digital documentation workflows and continuous compliance tracking strengthen long-term client engagement. Growth in emerging markets also presents opportunities, as regional companies increasingly seek regulatory support to access international markets and align with evolving global standards. Rising demand for regulatory guidance across biologics, combination products, and complex therapeutic areas positions outsourced consulting services as a critical component of development and commercialization strategies.
November 2024: Odyssey Health selected Syneos Health to assist in its concussion treatment trial, offering regulatory review services for the clinical development plans involving Odyssey's concussion drug ONP-002 and innovative intranasal device.