Quality Policy for the Supply of Pharmaceuticals and Medical Devices

Quality Policy for the Supply of Pharmaceuticals and Medical Devices


To fulfil one of the top priorities and commitments of our top management by developing and operating a quality management system in accordance with ISO/DIS 13485:2016 that sets high standards and the best practices which comply with the mandatory requirements on supplies of pharmaceutical products and medical devices.


We expect every employee and contractor to adhere to this policy and help reach our goals by:

  • continually and effectively enhancing our performance in quality assurance;
  • complying with standards required by the applicable regulatory ordinances;
  • ensuring the products safety, quality, efficacy and fitness for their intended use;
  • fulfilling the internal requirements prescribed by the Company;
  • promoting the quality policy and practices within the Company;
  • setting and reviewing measurable quality objectives;
  • minimising quality cost wherever practicable;
  • enhancing internal awareness of hazardous situations;
  • performing the risk assessment and implementing the effective risk management;
  • monitoring the residual risks;
  • reducing and preventing products contamination, cross-contamination, counterfeit and mix-ups where possible;
  • minimising the chance of product recalls;
  • minimising the possible adverse situations of consumer after use of our products;
  • advocating “good distribution practices” on both departmental and individual levels;
  • effectively communicating our quality performance to stakeholders; and
  • reviewing the overall performance of the quality management system and its continual suitability
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