Pharma to Market has put together a number of factsheets regarding the registration of pharmaceuticals and medical devices in various countries. To view them, please refer to the sidebar on the left.

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Factsheet: Biologic and Biosimilar Registration in Singapore

This document outlines the requirements for biologic and biosimilar registration in Singapore, including application routes, timelines and documentation required, such as GMP certificates, clinical trial data and dossier format. Download here →

 

Factsheet: Drug Registration in Malaysia

This document outlines the requirements for drug registration in Malaysia, including application routes, timelines and documentation required, such as GMP certificates, clinical trial data and dossier format. Download here →

 

Infographic: Drug Registration in Singapore

This document outlines the requirements for drug registration in Singapore, including application routes, timelines and documentation required, such as GMP certificates, clinical trial data and dossier format. Download here →

 

Infographic: Drug Registration in Malaysia

This document outlines the requirements for drug registration in Malaysia, including application routes, timelines and documentation required, such as GMP certificates, clinical trial data and dossier format. Download here →

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