The regulatory and approval of drugs in Singapore is a rigorous and comprehensive process. This is to ensure the safety, quality, and efficacy of drugs sold in the country. Although the process may be complex and time-consuming, people generally consider it transparent, predictable, and science-based. The significant market for therapeutic products in Singapore is expected […]
Read More →For medical device companies looking to enter the Singapore market, the registration process can be complex and time-consuming. However, it is a necessary step to ensure compliance with regulatory requirements and bring products to market. The medical device industry in Singapore has seen significant growth in recent years. The market is driven by a number […]
Read More →Singapore has become a global center for the pharmaceutical industry due to its cost-effective and reliable medical services, high-quality pharmaceutical manufacturing and research, access to regional markets, and skilled workforce. Also, the Government has supported several schemes to drive innovation and development. This has created many manufacturers to register their generic products in Singapore. The […]
Read More →Singapore has a well-established regulatory framework for clinical trials, overseen by the Health Sciences Authority (HSA). The HSA ensures that clinical trials conducted in Singapore adhere to ethical principles and Good Clinical Practice (GCP) guidelines. This article was last updated on 14/03/23. Singapore is considered as the R&D pioneer in Asia with highly qualified clinicians, […]
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