-

Global Road Construction Project Insights Report 2025: $3.89 Trillion in the Current Pipeline - Track the Top 20 Projects Per Region by Country, Stage, Value of Projects - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Project Insight - Global Road Construction Projects (Q3 2025)" report has been added to ResearchAndMarkets.com's offering.

The global road projects pipeline, as tracked by the analyst, is valued at $3.89 trillion.

North-East Asia accounts for the largest share of global value, with a pipeline valued at $1 trillion. The road project pipeline in South Asia totals $659.8 billion, ahead of South-East Asia, which records a pipeline of $473 billion, and North America with a pipeline value of $435.1 billion.

The global road projects pipeline is heavily skewed towards projects in the later stages of development, with the combined value of projects in the pre-execution and execution stages accounting for $2.7 trillion of the global pipeline value, representing a 70% share. Assuming all projects proceed according to schedule and spending is distributed evenly across the execution stage, annual pipeline expenditure may reach $444 billion in 2025. Between 2026 and 2029, spending on the currently tracked pipeline may reach an annual average of $453.7 billion

Report Scope

  • The report provides analysis based on the analyst's construction projects showing total project values and analysis by stage and funding for all regions. The top 20 projects per region are listed giving country, stage, value of projects. Ranked listings of the key operators for the sector are also provided showing the leading contractors, consulting engineers and project owners.

Reasons to Buy

  • Gain insight into the development of the road construction sector.
  • Assess all major projects by value, start date, scope and stage of development globally, for the regions to support business development activities.
  • Plan campaigns by country based on specific project opportunities and align resources to the most attractive markets.

For more information about this report visit https://www.researchandmarkets.com/r/od8bky

About ResearchAndMarkets.com

ResearchAndMarkets.com is the world's leading source for international market research reports and market data. We provide you with the latest data on international and regional markets, key industries, the top companies, new products and the latest trends.

Contacts

ResearchAndMarkets.com
Laura Wood, Senior Press Manager
press@researchandmarkets.com
For E.S.T Office Hours Call 1-917-300-0470
For U.S./ CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900

Industry:

Research and Markets

Release Versions
English

Contacts

ResearchAndMarkets.com
Laura Wood, Senior Press Manager
press@researchandmarkets.com
For E.S.T Office Hours Call 1-917-300-0470
For U.S./ CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900

More News From Research and Markets

Computer System Validation (CSV) Training Course: Regulations Impacting Your Systems and Hands-on Practice Writing Validation Documents (Jan 27th - Jan 29th, 2026 & On-Demand) - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Computer System Validation (CSV) Training Course (Jan 27th - Jan 29th, 2026)" training has been added to ResearchAndMarkets.com's offering. A course designed to completely immerse you in computer system validation. This course delivers comprehension of the regulations impacting your systems and hands-on practice writing validation documents. You will leave ready to lead efficient, effective, inspection- ready validation projects. Registration Includes: Checklist of...

Understanding Medical Device Regulatory Pathways - 510(k), PMA & Exemptions Webinar - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Understanding Medical Device Regulatory Pathways - 510(k), PMA & Exemptions (January 15, 2026)" training has been added to ResearchAndMarkets.com's offering. This expert-led 3-hour webinar provides a comprehensive introduction to the key regulatory pathways for medical device submissions in the US market. The regulation and control of new or substantially changed medical devices for sale in the US is based on the 510(k), PMA or DeNovo submission process. This w...

Medical Devices: Section 522 of the Federal Food, Drug, and Cosmetic Act (FD&C Act) Course: Developing Effective Post Market Surveillance and Complaint Handling Systems Training - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Course (Jan 22nd - Jan 23rd, 2026)" training has been added to ResearchAndMarkets.com's offering. What are U.S. FDA CGMP expectations/requirements for Post Market Surveillance and Complaint Handling? This seminar will examine Section 522 of the Federal Food, Drug, and Cosmetic Act (FD&C Act), as well as appropriate articles / Annexes of the EU's MDR, which require manu...
Back to Newsroom