Successfully registering your IVD device is the first step towards establishing a strong market presence in Indonesia. It enables collaborations with local distributors, healthcare institutions, and government programs. Additionally, it lays the foundation for future product launches and market expansion strategies.
Registering your IVD device ensures compliance with the regulatory requirements set by the Indonesian Ministry of Health. This compliance not only helps in avoiding legal issues but also builds trust and credibility with healthcare providers.
The demand for advanced diagnostic solutions is on the rise in Indonesia, driven by increased healthcare spending and a growing awareness of the importance of early disease detection. By registering your IVD device in Indonesia, you tap into a large and emerging market with significant growth potential.
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ANDAMAN MEDICAL PTE LTD (Head Office Singapore)
Tampines Junction Business Center
Level 09-02, 300 Tampines Avenue 5,
Singapore 529653
