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To facilitate the conduct of single-dose and repeated-dose animal toxicology studies in accordance with 10 OECD-GLP Principles and OECD Testing Guidelines.
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To facilitate the conduct of single-dose and repeated-dose animal toxicology studies in accordance with international guidelines such as the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), U.S. Food & Drug Administration (FDA), and European Medicines Agency (EMA).
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To conduct animal toxicology studies in accordance to 10 OECD-GLP Principles, OECD Testing Guidelines for Malaysian Herbal Monograph.
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To provide consultation to inquiring governmental or private bodies on GLP animal toxicology studies.
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To conduct general and specialised training for NCRF, IMR personnel and in-house staff.
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To engage and coordinate with the Compliance Monitoring Authority (CMA) of National Pharmaceutical Regulatory Agency (NPRA) or surveillance inspections, test facility visits, meetings, training and many more.
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To perform maintenance and monitoring of NCRF, IMR facility in accordance to GLP Principles and OECD-GLP certification.
