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Hear from SAI Global Assurance CEO, John Rowley, about key issues facing the Assurance Industry globally.

Medical Device manufacturers around the globe are uniquely affected in this time of the COVID-19 Pandemic. Medical device products and services continue to be in high demand, and essential for hospitals and patient care providers. Medical device manufacturers are facing new challenges with being able to manufacture, procure and/or distribute critical medical products and components during this unprecedented period.

To mark the 10th anniversary of World Accreditation Day SAI Global’s Paul Phyall, Director, UK & Ireland, Assurance, discusses how accreditation can deliver a safer world.

Research reveals bullying and harassment prevalent in 1 in 3 workplaces – with peers among the major perpetrators

During this webinar we'll discuss how you could improve your facilities food safety and compliance in just 1 day

What is the future of nutritional labeling and how do we stay ahead of challenges?

The Medical Device Single Audit Program (MDSAP) was created by the International Medical Device Regulators Forum (IMDRF) to enable audits that encompass ISO 13485 as well as the regulatory requirements from the United States, Canada, Australia, Brazil and Japan.

Preparing for and responding to issues and crises is a commonly experienced task for all organisations around the world.

View a complimentary on-demand webinar on maximizing value from your SQF program.