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Jun 10, 2025

MIV-2 Notification vs MIV-2 Do-and-Tell: What you need to know prior to submission
Jun 03, 2025

Are Biologics Always NDA-1 in Singapore? A Guide to Regulatory Categories
May 28, 2025

Biologics in Singapore: What Makes the Dossier Different?

Commercializing your product through regulatory classification

Regulatory classification can definitely put your product at an edge over your competitor if you are able to evaluate and understand the intended market audience and your product positioning.

31 Mar 2022 |
Pharmaceutical Consulting

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What is a ASEAN CTD ?

In my previous blog, we shared briefly on 5 points to look out for when preparing a dossier for submission

31 Mar 2022 |
Pharmaceutical Consulting

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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!