Julphar's main objective is to ensure our patients' safety by producing high quality products through our world-class facilities. This is achieved through our Quality Assurance system which enables us to integrate quality into all stages of manufacturing.

The Quality Assurance system objective is to incorporate current Good Manufacturing Practices (cGMP), comply with local and international regulatory requirements – UAE Ministry of Health (MOH), US Food and Drug Administration (FDA) Title 21 of the Code of Federal Regulations (CFR) part 210/211, EU Good Manufacturing Practices (GMP), International Conference on Harmonisation (ICH), World Health Organization (WHO) guideline – and aim for continuous improvement.

The facilities, manufacturing operations and Quality Assurance system are accredited by ISO 9001:2008, as well as different regulatory bodies to ensure all practices at Julphar are aligned with international requirements.