Regulatory information related toCOVID-19by NPRA

FAQ COVID-19 Vaccine

FAQ COVID-19 Vaccine

FAQ: Hand Sanitizers

FAQ: Hand Sanitizers

Cosmetics Section's compilation of Frequently Asked Questions regarding hand sanitizers.

Circular and Directive

Circular and Directive

on Covid-19 Pandemic

Press Releases on AEFIs of COVID-19 Vaccines

Press Releases on AEFIs of COVID-19 Vaccines

Official Notice for Site Inspections

Temporary Suspension for Site Inspections

Official notice for temporary suspension for inspection in and out of Malaysia for GMP, GDP, GCP and GLP and BE Research Centers.

Voluntary Registration of Surface Disinfectant

GUIDELINE FOR THE REGISTRATION OF SURFACE DISINFECTANT

Lot Release for

COVID-19 Vaccines

Lot Release for

COVID-19 Vaccines

Summary Reports on AEFIs of COVID-19 vaccines

Summary Reports on

AEFIs of COVID-19 vaccines

FAQ: Clinical Trials

FAQ: Clinical Trial

Guidance from Evaluation and Safety of Investigational Product Section on Managing Clinical Trials during the Covid-19 Pandemic in Malaysia.

FAQ: GMP & GDP Inspections

FAQ: GMP & GDP Inspections

FREQUENTLY ASKED QUESTIONS ON GOOD MANUFACTURING PRACTICE (GMP) AND GOOD DISTRIBUTION PRACTICE (GDP) INSPECTIONS BY NATIONAL PAHARMACEUTICAL REGULATORY AGENCY (NPRA) DURING COVID-19 PANDEMIC

 

Reporting ADR (including drugs used for COVID-19 treatment)


Please report ALL suspected Adverse Drug Reactions (ADRs) to the National Centre for Adverse Drug Reactions Monitoring.
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National Pharmaceutical Regulatory Agency (NPRA)

Lot 36, Jalan Universiti (Jalan Prof Diraja Ungku Aziz), 46200 Petaling Jaya, Selangor, Malaysia.

  • Phone: +603-7883 5400

 

 

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