We at Relisys Medical Devices Limited are committed to:

• Develop & produce medical devices conforming to International standards that ensure highest safety and claimed efficacy
• Ensure delivering of quality products that meet all the requirements of customer and regulatory norms
• Continue to conduct professional training at all levels to increase the knowledge and competency of employees
• Provide all the resources needed to implement an effective quality management system
• Improvement at all stages of operations and strive to be the industry leader
• Be rated as the benchmark in all areas of operation

Relisys has adopted International Standard, EN ISO 13485:2016 and thus we are committed towards the specified requirements for QMS in order to:

• Demonstrate its ability to consistently provide and ensure the supply of products manufactured & services provided by Relisys are consistently conforming to customers, applicable standards and prevailing regulatory requirements
• Meet customer & regulatory requirements through the effective application of the system, including the processes for improvement of the system and the assurance of conformity to customer and applicable statutory and regulatory requirements
• Tighten the Scope of Relisys, for each of the process stages such as Design, Manufacture, Assembling, Sterilization, Storage & Dispatch which includes life cycle of a device