The changes to ISO/IEC 27001 and ISO/IEC 27002 in 2022 represent a leap forward in the effectiveness of Information Security Management Systems (ISMS). Quick and effective adoption of the latest global best practice is essential to ensure trust in your organization’s ability to protect information.

In today’s constantly changing cyber landscape, it’s important for organizations - regardless of their size and sector – to evolve the way they manage the complexity of modern security threats and IT infrastructure. The revised version of ISO/IEC 27002:2022, outlines the changes made to the standard, highlighting how this third edition has been modernized and simplified to make adoption easier, versatile and more effective; and detailing what the changes might mean for users of the standard.

Despite being the world’s second largest casting manufacturer, India lags when it comes to the final quality of the products. This gap is more visible when we realize that only a few MSME and large-scale foundries are qualified to export their products to markets like EU, UK, Australia and US. India with its huge potential should compete with others and secure its deserved position as a quality manufacturing hub. 

The industrial automation and control systems (IACS) sector is having great opportunities due to Industry 4.0 and Industrial IoT. Along with these possibilities come security risks; to avoid equipment damage, downtime, and safety concerns, industrial environments must be ready for growing cyberattacks. Industries today need a structured approach to assess various levels of threats at various levels. Furthermore, as government policies and regulation in this field are emerging, it is important to ensure your products meet market entry requirements.

The need for rigorous compliance with regulations and strict adherence to best-practice surrounding the quality, safe, and efficient manufacturing and distribution of medicines has never been greater.

With this joint roundtable session, our goal is to discuss and debate smart quality approaches in the pharmaceutical sector to help promote, standardize, monitor, and assess adherence to the GMP (good manufacturing practice) and GDP (good distribution practice) regulations that underpin the pharmaceutical industry.

To improve audit quality, and to maximise the effectiveness of the time
spent on site. It has the potential to provide a more cost-efficient process
through the sharing and reviewing of information ahead of the site visit.