ISO 13485 Certification is the globally recognized standard for Quality Management Systems (QMS) in the medical device sector. It provides objective evidence that a manufacturer’s design, production, and distribution...
Steps for QC 080000 Certification 1. Write manual and procedures required for QC 080000 2. Training on the importance of QC 080000, Identifying the Hazardous substances in vogue, Preparation...
What you need to know about ISO 13485? ISO 13485 is intended to be utilized by associations engaged with the plan, creation, establishment and overhauling of clinical gadgets and...
If management conforms that they are meeting all the appropriate and international standards and also provides a proper endorsement that the system is in place, then the organization will...
Are you concerned about the credibility of the ISO 13485 certification? As medical professional or medical devices public procurement officer, you must know whether the medical devices which you...
14th October 2020 – World Standards Day – SKY is the LIMIT Want to Learn more – email to [email protected]
ISO 13485 Consultancy by IRCA Approved auditors with excellent experience in ISO 13485 audit experience in Medical devices such as Dental equipments, Elisa type readers, Trading companies, Servicing of...
RISKS AND OPPORTUNITIES – REFLECTION ON RISK MANAGEMENT One of the key requirements of an ISO framework is managing risks and opportunities. The focus is not just on risks...
Remote Online ISO Certification due to Covid 19 Virus issue – valid until December 2020 GQS Singapore becomes the first South East ISO Certification body to announce remote ISO...