Information to share

Date: 31st May 2025, Time / Duration: 3:00 PM to 5:00 PM IST, Mode: Online  Click to Join the Webinar –  https://teams.microsoft.com/l/meetup-join/19%3ameeting_YjRjMTdkMGUtYTUyMS00ZTZkLTg2NGEtMWMyOWI5M2NmY2Nh%40thread.v2/0?context=%7b%22Tid%22%3a%221c320fbb-a48f-46a8-b949-03e566ab764d%22%2c%22Oid%22%3a%22315216f7-c970-48f0-9c57-8cd28a15cc3f%22%7d  Speaker: Mr. Arunendra Dvivedi – MD cum Speaker for ISO/IEC 27001 Standard  CLICK -  https://docs.google.com/forms/d/1H8bI4zhoUzF-Kfc_jMG9mgpmW4KXR2FEhdzScHWcbbA/edit  

  Facility management (FM) plays a crucial role in ensuring the smooth operation of buildings, infrastructure, and support services. In New Zealand, where sustainable and efficient property management is gaining more attention, ISO 41001 certification in New Zealand is becoming an essential standard for organizations aiming to enhance performance, sustainability, and stakeholder satisfaction.   In this blog, we’ll explore what ISO 41001 is, why it’s important in New Zealand , and how your organization can achieve certification.   What is ISO 41001? ISO 41001:2018 is the international standard for Facility Management (FM) systems. It provides a structured framework to improve the effectiveness and efficiency of FM operations by aligning them with an organization’s strategic direction.   The standard covers:   Strategic planning of facilities   Operational performance and maintenance   Health and safety of occupants   E...

  In today’s competitive global market, maintaining quality, safety, and efficiency is not just an advantage—it’s a necessity. ISO certification in Canada has become a widely recognized benchmark for organizations striving to improve operations and build trust. But what exactly is ISO International Organization for Standardization certification , and why is it so important for businesses operating in Canada? Let’s break it down. What is ISO Certification? ISO certification refers to the process by which a company’s management system, process, or service is verified to comply with standards developed by the International Organization for Standardization (ISO) . These standards ensure that products and services are safe, reliable, and of good quality . There are many types of ISO standards, each focused on a different aspect of business. Some of the most common include: ISO 9001 – Quality Management Systems in canada ISO 14001 – Environmental Ma...

   Introduction ISO certification is a powerful tool for Canadian businesses seeking to demonstrate their commitment to quality, consistency, and continuous improvement. Whether you're targeting  ISO 9001 Quality Management system in canada ,  ISO 14001 Environmental Management system in canada ,  ISO 45001 Occupational Health & Safety management system in canada , or another ISO standard, the certification process follows a structured path. This guide outlines  six essential steps  to achieving ISO certification in Canada—making your journey clear, manageable, and efficient. Step 1:  Understand the Standard and Define Objectives The first step is choosing the right  ISO standard in canada  based on your business goals. For example: ISO 9001  for quality management ISO 14001  for environmental sustainability ISO 45001  for workplace safety ISO 27001  for information security ISO 13485  for medical device qual...

  In the rapidly evolving medical device industry, regulatory compliance and quality management are critical to success. ISO 13485 is the international standard that outlines requirements for a comprehensive quality management system (QMS) specific to the design and manufacture of medical devices. For businesses in Canada achieving ISO 13485 certification not only supports compliance with Health Canada regulations but also opens doors to global markets.   This guide offers a complete overview of ISO 13485 certification in Canada —what it is, why it's important, and how to get certified.   What is ISO 13485? ISO 13485 is a globally recognized standard developed by the International Organization for Standardization (ISO). It specifies the requirements for a quality management system for organizations involved in the design, production, installation, and servicing of medical devices and related services.   While ISO 13485 is based on ISO 9001, it includes...