NPRA Malaysia Publishes Updates on Guidance and Requirements on Conditional Registration of Pharmaceutical Products During Disaster
National Pharmaceutical Regulatory Agency (NPRA) Malaysia has issued the third revised version of the guidance and requirements on conditional registration …
Hong Kong Drug Office Publishes Guideline on Pharmaceutical Products Recall
Hong Kong Drug Office has published some guidelines on the recall of pharmaceutical products in March 2022. Pharmaceutical products are …
Singapore HSA Announces Requirement for Notification of Lot Release Information of Imported Vaccines
The Health Sciences Authority (HSA) Singapore has published an update regarding the notification of lot release information of imported registered …
Australia TGA Publishes Latest Guidance on Reclassification of Active Implantable Medical Devices
The Therapeutic Goods Administration (TGA) Australia has published the latest document on the reclassification of active implantable medical devices (AIMD) …
NPRA Malaysia Publishes Frequently Asked Questions on Medicinal Gases
National Pharmaceutical Regulatory Agency (NPRA) Malaysia has issued a set of frequently asked questions (FAQs) on medicinal gases in February …
Singapore HSA Publishes Guidelines on Voluntary Electronic Labelling for Complementary Health Products
The Health Sciences Authority (HSA) Singapore has published a guidance document on voluntary electronic labelling for complementary health products (CHP) …
Hong Kong Drug Office Publishes Guidance Notes on Registration of Pharmaceutical Products
Hong Kong Drug Office has published some guidance notes on the requirements of pharmaceutical products in February 2022. Registration of …
Singapore HSA Publishes Revised Guidance on Health Supplements Guidelines
The Health Sciences Authority (HSA) Singapore has published the latest guidance document on health supplements in March 2022. The working …
Australia TGA Publishes Information on Regulation Essentials
The Therapeutic Goods Administration (TGA) Australia has published a general overview of the regulatory process, along with information about relevant …