- Develop and implement advanced diagnostic techniques for the identification and management of Inborn Errors of Metabolism (IEM) / Rare Genetic Disorder.
- Increase the efficiency and accuracy of screening processes for metabolic disorders using state-of-the-art technologies.
- Provide rapid and reliable testing to ensure early diagnosis, which is critical for timely intervention and treatment.
- Continuously broaden the range of biochemical and genetic tests offered, including those for disorders not yet available in Malaysia.
- Collaborate with clinicians to identify emerging diagnostic needs and enhance patient care.
- Engage in research activities to innovate and optimize diagnostic methodologies for biochemical genetics.
- Provide training and education to healthcare professionals and students in biochemical testing and its clinical applications.
- Maintain high standards of quality control and assurance in all laboratory processes and diagnostic tests.
