INTRODUCTION OF ISO 41001:2018 (FACILITY MANAGEMENT) Facility management (FM) integrates a couple of disciplines so that you can have a power at the performance and productiveness of economies of societies,…
WHY CAN’T WE THROW THE ELECTRONIC DEVICES IN REGULAR DUSTBINS ? Electronic devices are made up of heavy metals like lead, mercury, cadmium, beryllium, PVC etc. If one throws e-waste…
What is IFS? IFS are a safety standard that applies to companies that sell, supply, and manufacture food products. It does activities like handling loses food, packing and processing. IFS…
The Basics for implementing ISO 50001: 2018 - Energy Management System The focus of all the leaders and the managers within a system will entirely depend upon the delivery of…
What is VAPT ? VAPT is a term used to describe security testing that is designed to identify and help address cyber security vulnerabilities and threats. VAPT includes testing and…
Purpose of ISO 13485 certification: Medical devices In the medical industry, this ISO 13485 certification is made to be the International Standard under the Quality Management System (QMS). The ISO…
ISO 13485: Medical devices – Quality management systems requirements for regulatory purposes Raw materials Components Subassemblies Medical devices Sterilization services Calibration services Distribution services Maintenance services Hence, the supplier or…
FujiFilms Japan one of the largest conglomerates in Sale, Installation, Service of various types of Medical devices having global presence has signed up with us for the support in ISO…
Difference between management system certification and product certification: ISO 13485 If management conforms that they are meeting all the appropriate and international standards and also provides a proper endorsement that…
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 purchase…
