Label & Artwork Review: Review and approve product labels, nutrition panels, ingredient lists, and packaging artwork to ensure strict compliance with local and export regulations.
Manage end-to-end regulatory submissions — including Investigational New Drug applications (INDs), Clinical Trial Applications (CTAs), amendments, safety reports, Development Safety Update Reports (DSURs), and annual reports — in full compliance with applicable regulations.
Manage end-to-end regulatory submissions — including Investigational New Drug applications (INDs), Clinical Trial Applications (CTAs), amendments, safety reports, Development Safety Update Reports (DSURs), and annual reports — in full compliance with applicable regulations.
Expand your technical finance skillset by owning month-end close, statutory reporting, and audit coordination across Malaysian requirements. Gain direct experience with MFRS compliance and regional filings.