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Regional Guides insights.

Market entry and regulatory strategy by geography

6 piecesUpdated Mar 01, 2026
Regional GuidesFeb 28, 2026

China Clinical Trials: Cost, Speed & Regulatory Advantages

Run clinical trials in China and save 60% on costs with 2-5x faster enrollment. NMPA IND process, MRCT strategy for FDA acceptance, BIOSECURE Act clarification, and China CRO landscape guide.

7 min
Regional GuidesFeb 28, 2026

NMPA Drug Approval Process: Complete Guide 2026

China's FDA equivalent explained. Complete guide to NMPA drug approval pathways, IND filing, Breakthrough Therapy Designation, Conditional Approval, and NDA timelines for global pharma companies.

6 min
Regional GuidesFeb 28, 2026

Top Chinese Biotech Companies to Watch in 2026

The definitive guide to China's most innovative biotech companies with active out-licensing pipelines. ADC, bispecific, GLP-1, CAR-T leaders and their global deal pipelines — organized by therapeutic area.

6 min
Regional GuidesFeb 16, 2026

The BIOSECURE Act: Impact on Pharma Supply Chains & China Partnerships

How the landmark legislation signed December 2025 reshapes global biopharma manufacturing, CDMO relationships, and cross-border deal strategy.

4 min
Regional GuidesFeb 16, 2026

Japan Pharma Market Entry Guide: Navigating the World's 3rd Largest Market

How to enter Japan's ~$90B pharmaceutical market. PMDA pathways, NHI pricing, partnership models, and cultural considerations.

4 min
Regional GuidesDec 21, 2025

China Biotech Licensing 2026: The Definitive Technical Guide

Navigating the world's second-largest market: From NMPA acceleration to the ADC licensing surge.

4 min
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