Sino Pharma Group
10x Faster Cross-Border Regulatory Submissions
10x
Faster Submissions
70%
Cost Reduction
3
Markets Simultaneously
The Challenge
Managing parallel drug registrations across China, Japan, and ASEAN required a team of 30+ regulatory affairs specialists and took 18-24 months per submission cycle.
Solution & Outcome
RegIntel reduced submission preparation time from 18 months to under 6 weeks by automating dossier generation, gap analysis, and real-time regulatory change tracking.
Related Cases
Precision BioSG
Clinical-Stage Biotech
AI-Driven Target Identification Cuts Discovery Time in Half
KyoPharma CMO
Contract Manufacturer
GMP Batch Failure Rate Slashed by 35%
MedCo ASEAN
Regional Pharma Co.
Market Access Strategy Powered by AI Insights
Start Your Digital Transformation
Discover how HealthTech Nexus can help your organization achieve breakthroughs