Singapore’s ePR Submission: A Seamless Digital Process
Singapore has digitised its Permanent Residency (PR) application process through the ePR submission system, an online submission platform introduced by the Immigration & Checkpoints Authority (ICA). This...
Enhancing Recruitment with Employ Africa: Your Gateway to Talent Across the Continent
In today’s competitive global market, finding the right talent can be a daunting challenge. Companies need skilled, experienced, and reliable employees to drive their...
The Power of Culture: Why a Strong Organizational Culture is Essential for Business Success
In the contemporary business landscape, where competition is fierce and market dynamics are constantly shifting, organizational culture has emerged as a crucial factor that...
Axis Global Co Named Finalist in International Business Excellence Awards 2024
Axis Global Co, a leader in the marketing and public relations industry, has been confirmed as an official finalist for the prestigious International Business...
EU CE Marking for Medical Device By I3CGlobal
To place a medical device on the EU market, it must adhere to the General Safety and Performance Requirements (GSPRs) and comply with all relevant EU directives. Upon successful completion of a conformity assessment procedure, compliance is indicated by affixing a CE mark on the medical device. Business
Introduction
To place a medical device on the EU market, it must adhere to the General Safety and Performance Requirements (GSPRs) and comply with all...
