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Nov 07, 2025

Common Pitfalls in Module 3 Submissions for Biologics And How to Avoid Them
Oct 24, 2025

HSA Pre-Submission Meetings: Why They Matter for New Drug and Biologic Approvals in Singapore
Oct 10, 2025

Why a Compliant PIF is Critical for Cosmetic Product Notification in Singapore — And How TRC Can Help

Understanding the Medical Device Registration Process in Singapore

In the world of healthcare, regulatory compliance is the foundation upon which patient safety and industry integrity are built. That is why when it comes to introducing a medical device to the Singaporean market, there are stringent demands of regulatory compliance to ensure utmost safety, reliability and efficacy. In this blog, we delve into the […]

15 Nov 2023 |
Quality Management

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How to set up a Quality Management System for a SME in medical field

A Quality Management System is a set of guidelines and operating procedures to ensure that the company meets its objectives to provide quality and efficient product and services.

31 Mar 2022 |
Quality Management

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Steps to get ready for an overseas on-site GMP inspection for pharmaceutical products in Singapore

If you are currently an overseas company having plans to get your manufacturing site to be (PIC/S) certified, Singapore is a best choice

30 Mar 2022 |
Pharmaceutical Consulting

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Hand picking pharmaceutical product for regulatory consulting in pharma

If you have any specific regulatory questions pertaining to entering the Singapore market or require assistance with pharma regulatory services and medical product registration, feel free to reach out. Your success in the pharmaceutical industry starts with us!