Author Archives: admin

How ISO/IEC 27001:2022 Fits in with All the Other Frameworks

In the ever-evolving world of cybersecurity and data privacy, many businesses find themselves juggling multiple frameworks, ISO/IEC 27001:2022, NIST, POPIA, GDPR, COBIT, CIS Controls and more. It can be overwhelming. But here’s the good news: ISO/IEC 27001:2022 is not in competition with these frameworks. It complements them. It provides a structured foundation that aligns well […]

The 5 Most Common Nonconformities… No need to be worried.

Hearing the word nonconformity during an ISO audit can make any organisation feel uneasy. But the truth is, nonconformities are a normal, and useful, part of the audit process. In fact, they’re opportunities to improve, not red flags for failure. Here are the five most common nonconformities we see across industries, and why you shouldn’t […]

What Is a Takeover Audit for ISO Certification?

What Is a Takeover Audit for ISO Certification?

Changing certification bodies (CBs) doesn’t mean starting your ISO journey from scratch. If you’re already ISO-certified and looking to switch to a different certification body, whether for better service, pricing, or turnaround times, you’ll go through what’s called a Takeover Audit. Also known as a Certification Transfer, a Takeover Audit allows an accredited certification body […]

Understanding Remote Audits for ISO/IEC 27001:2022 and the ISO 17021 Standard Requirements

Sancert - Remote Auditing

In today’s business landscape, remote audits have become an essential part of the certification process, especially for standards like ISO/IEC 27001:2022, which focuses on Information Security Management Systems (ISMS). The COVID-19 pandemic accelerated the use of remote audits, but the shift to digital has proven to be not just a necessity but also an efficient, […]

SAHPRA Now Requires ISO 13485:2016 Certification – Sancert Is Ready to Help You Comply

In a significant regulatory shift, the South African Health Products Regulatory Authority (SAHPRA) has announced that from 1 June 2025, all manufacturers, importers, and distributors of medical devices and IVDs must hold a valid ISO accredited 13485:2016 certification to apply for, renew, or amend a Medical Device Establishment Licence. This isn’t just a policy update […]

Racing Towards Excellence: What the ABSA Cape Epic and ISO Certification Have in Common

At first glance, the Absa Cape Epic and ISO certification may seem worlds apart—one is a grueling mountain bike race across some of the toughest terrain in the world, while the other is a structured process for achieving operational excellence. But when you take a closer look, they share far more than you’d expect. Just […]

Accredited vs. Non-Accredited ISO Certification Bodies – Why It Matters

Achieving ISO certification is a significant milestone for any business, demonstrating commitment to the internationality recognised quality, environmental and information security standards. However, not all ISO certifications carry the same level of credibility. The difference lies in whether the certification body is accredited or non-accredited. Choosing the right certification body impacts how your certification is recognized, […]

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