Frequently Asked Questions

Syndesia provides comprehensive support including regulatory and quality (RAQA) compliance, manufacturing partnerships, clinical trial management, commercialization strategy, and growth-stage advisory. We offer end-to-end guidance from concept to market success.

Our RAQA team provides ISO 13485 certification support, CE marking documentation, FDA pathway planning, and virtual regulatory office services. We ensure compliance is built into every stage of development, streamlining regulatory approval across multiple jurisdictions in SEA and APAC.

Yes. We guide you through production design optimization, cost efficiency, and supply chain management. Our vetted supplier partnerships across Asia-Pacific ensure regulatory-grade manufacturability, helping you deliver high-quality medical devices at scale while maintaining compliance.

We offer strategic clinical trial planning, access to investigator networks across SEA and APAC, usability studies, and Key Opinion Leader (KOL) collaboration. Our clinical evaluation support demonstrates efficacy and safety, positioning your innovation for successful regulatory approval and market access.

We provide commercialization strategy, hospital integration support, pricing optimization, and distribution partnerships to accelerate MedTech adoption. Our go-to-market execution helps achieve sustainable growth through value-based adoption, strategic positioning, and proven market access channels.

Syndesia primarily focuses on Southeast Asia and APAC markets, including Singapore, Malaysia, Thailand, Indonesia, Philippines, and Australia. We also support international expansion strategies for mature MedTech ventures seeking global market opportunities.

Yes. We provide Malaysia relocation and residency support services, helping international founders and teams with seamless integration into the local business ecosystem. We also offer family office setup and management support across Singapore and Malaysia.

You can reach us through our contact form on the website, via email, or schedule a consultation call. We respond within 24 hours to all inquiries. You can also explore our market access programs and mission trip initiatives for networking opportunities.