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Consumer Reporting of Side Effects to Medicines or Vaccines. To report a suspected side effect or adverse drug reaction (ADR) to any medicine (including prescription, over-the-counter, traditional product, health supplement, etc.) or adverse event following immunisation (AEFI) to any vaccine.
Jun 26, 2024 · All words Any words Exact Phrase. Ordering: Search Only: Documents Images Videos Blogs Documents SP Page Builder Books Book Pages Search Events Categories Contacts Articles News Feeds Tags K2 Items. Last Modified: Wednesday 26 June 2024, 10:25:10.
QUEST 3+ Product Search. The search result displayed is only applicable on the date and time of when the search was conducted. Hasil carian yang dipaparkan hanya terpakai pada tarikh dan masa apabila carian dijalankan. The product / cosmetic under NPRA regulatory control status is subjected to changes according to regulatory update / needs.
The search result displayed is only applicable on the date and time of when the search was conducted. Hasil carian yang dipaparkan hanya terpakai pada tarikh dan masa apabila carian dijalankan. The product / cosmetic under NPRA regulatory control status is subjected to changes according to regulatory update / needs.
Jun 28, 2024 · Regulatory Information. Product Classification, QUEST3+ System Basic, ASEAN Guidance Documents, Guideline For The Submission Of Product Samples For Laboratory Testing & Clinical Trials. Regulation Basic. Among the pharmacovigilance activities carried out by NPRA are adverse drug reaction (ADR) monitoring and screening of drug safety alerts.
Jun 28, 2024 · The purpose of the Principles of GLP is to promote the development of quality data. Good Laboratory Practice (GLP) Any company that want to manufacture, import or wholesale any registered products need to have Manufacturer’s License, Import License or Wholesale License. Licensing & Certification Section is involved in the activity of issuance ...
Industri. Pendaftaran Produk, Sistem QUEST3+, Garis Panduan, Borang Permohonan, FAQs. National Pharmaceutical Regulatory Agency (NPRA), Ministry of Health Malaysia. Malaysia Drug Control Authority.
