Catalyzing Healthcare Innovation
Indonesia's integrated Contract Research Organization.
Most sponsors run a single study across three vendors — a CRO, a laboratory, and a regulatory consultant.INCREASE delivers all three in one place, so your data, your timeline, and your submission stay aligned from ideation to market access.
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Sponsor
Countries
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Clinical
Sites
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Provinces
Across Indonesia
ISO 9001:2015 certified Quality Management System
View our portfolioWhat we do
Speed Advantage
Early laboratory integration and parallel regulatory and site activation cut study startup time by up to 50%.
*Based on internal project benchmark. Actual timelines are estimates and may vary depending on study complexity and project requirements.
Better Data
Faster Timeline
Lower Risk
End-to-end Capabilities
Stage 1
Protocol aligned with laboratory and regulatory requirements from day one.
Stage 2
Pre-qualified sites, with ethics and regulatory submissions run in parallel.
Stage 3
Patient recruitment, site management, and in-house sample handling.
Stage 4
Centralized laboratory testing and a unified, submission-ready dataset.
Stage 5
Regulatory submission support and post-approval lifecycle management.
Partnership & Collaboration
Tell us where your programme stands and our team will map the fastest compliant route to market.