PUTRAJAYA, Nov 5 — Updates to the Guideline For Facilitated Registration Pathway (GFRP), to be effective from Jan 1, were approved during the meeting of the Drug Control Authority (PBKD) on Nov 3, as part of efforts to strengthen the Facilitated Registration Pathway (FRP).

PUTRAJAYA, April 6 — The Ministry of Health (MOH) has agreed to give 'orphan medicine’ status to Koselugo Hard Capsules 10mg and 25mg, said Health Director-General Tan Sri Dr Noor Hisham Abdullah.

KUALA LUMPUR, March 23 — The Ministry of Health (MOH) has issued a cancellation and recall on all registered products containing pholcodine.

KUALA LUMPUR, Feb 21 — The Pfizer-BioNtech vaccine is the first Covid-19 vaccine given conditional registration approval by the Drug Control Authority (DCA) and the National Pharmaceutical Regulatory Agency (NPRA) after going through the proper evaluation process and its use will be closely monitored.