Congratulation to Lifeways Sdn. Bhd. for being certified according to ISO 13485 standard.
The Malaysian Medical Device Act (MDA) 2012 has enforced Medical Device Industry to comply regulation pertaining requirements and procedure matters. Among of these, ISO 13485 certification is one of compulsory requirement that local Manufacturers need to submit for their license establishment. Approved ISO 13485 certificate not only evidences that provided products are produced safely, manufactured in good manufacturing practice but also labelled, packaged, marked in according to prescribed manner under regulation of Authority.
Lifeways Sdn. Bhd., a Manufacturer in fields of Medical, Diagnostic, Laboratory, Scientific and Home Care, has continuously developed their products with purpose of improving human life. In order to ensure provided products to market is conformed to essential principles of regulation requirement, Lifeways Sdn. Bhd. has been successfully passed initial audit assessment conducted by DQS Certification Sdn. Bhd. in July 2016.
Mr. Danny Ng DQS Regional Managing Director (3rd from Left) taken group photo together with Lifeways management and staffs.
Choosing DQS to be their Conformity Assessment Body (CAB# 006), Lifeways has lightened an inspiration into their quality management system. Not only so, won certificate benefits Lifeways confidence to introduce their products to markets to catch up with the rapid speed of development in Medical Industry. After audit assessment, DQS’s Auditor commented that the readiness of preparation upon auditing proves Lifeways very much cares about the commitment to their customers.
Being an appointed CAB of Lifeways for their ISO 13485 certification, this is not only our honour but also our responsibilities to add in their strengths, improve and bridge potential preventive actions for organization.