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ISO 22716
Featured 15.07.2026 · 3 min read

ISO 22716 Explained Section by Section: The Full Series

A complete guide to ISO 22716, the international cosmetics GMP standard, working through every section with links to a detailed explanation of each.

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ISO 22716 Section 17 Explained: Documentation — The Backbone of GMP Compliance ISO 22716

14.07.2026 · 3 min read

ISO 22716 Section 17 Explained: Documentation — The Backbone of GMP Compliance

ISO 22716 Section 17 covers documentation — the requirement that underpins every other section of the standard. Here is why it deserves standalone attention.

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ISO 22716 Section 16 Explained: Internal Audit Requirements ISO 22716

13.07.2026 · 3 min read

ISO 22716 Section 16 Explained: Internal Audit Requirements

ISO 22716 Section 16 sets out how internal audits should be approached, who should conduct them, and what happens to the findings.

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ISO 22716 and BRCGS: How Cosmetics GMP Maps to Enhanced Hygiene Expectations Compliance Insights

13.07.2026 · 3 min read

ISO 22716 and BRCGS: How Cosmetics GMP Maps to Enhanced Hygiene Expectations

Cosmetics manufacturers running ISO 22716 are better prepared for BRCGS Consumer Products Issue 5 enhanced hygiene expectations than they might think. Here is how the two map.

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ISO 22716 Section 14 Explained: Complaints and Recalls ISO 22716

12.07.2026 · 3 min read

ISO 22716 Section 14 Explained: Complaints and Recalls

ISO 22716 Section 14 covers how complaints should be investigated and how a product recall should be coordinated if it becomes necessary.

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ISO 22716 Sections 13 and 15 Explained: Deviations and Change Control ISO 22716

11.07.2026 · 3 min read

ISO 22716 Sections 13 and 15 Explained: Deviations and Change Control

ISO 22716 Sections 13 and 15 are both brief but cover a critical distinction — planned changes versus unplanned, temporary departures from specified requirements.

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ISO 22716 Section 12 Explained: Subcontracting Requirements ISO 22716

10.07.2026 · 3 min read

ISO 22716 Section 12 Explained: Subcontracting Requirements

ISO 22716 Section 12 sets out the obligations of contract givers and contract acceptors. Here is what needs to be in place when any part of GMP-covered work is outsourced.

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COS-GMP Explained Section by Section: The Full Series COS-GMP

10.07.2026 · 3 min read

COS-GMP Explained Section by Section: The Full Series

A complete guide to COS-GMP, Apex Global Quality's cosmetics GMP standard, working through every section with links to a detailed explanation of each.

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COS-GMP Section 13 Explained: Design and Development COS-GMP

09.07.2026 · 3 min read

COS-GMP Section 13 Explained: Design and Development

COS-GMP Section 13 covers product design and development, labelling, and claims legality — ground that ISO 22716 does not address at all.

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ISO 22716 Section 11 Explained: Waste Management Requirements ISO 22716

09.07.2026 · 2 min read

ISO 22716 Section 11 Explained: Waste Management Requirements

ISO 22716 Section 11 is short but specific about how waste should be classified, handled, and disposed of without creating a contamination risk.

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ISO 22716 Section 10 Explained: Treatment of Product That Is Out of Specification ISO 22716

08.07.2026 · 2 min read

ISO 22716 Section 10 Explained: Treatment of Product That Is Out of Specification

ISO 22716 Section 10 covers what happens to rejected and reprocessed product once a result has confirmed it does not meet specification.

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COS-GMP Section 12 Explained: Inspections and Acceptance COS-GMP

08.07.2026 · 3 min read

COS-GMP Section 12 Explained: Inspections and Acceptance

COS-GMP Section 12 covers test methods, acceptance criteria, sampling, and retain samples — broadly equivalent to ISO 22716's quality control laboratory section.

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COS-GMP Section 11 Explained: Storage and Despatch COS-GMP

07.07.2026 · 3 min read

COS-GMP Section 11 Explained: Storage and Despatch

COS-GMP Section 11 covers storage, positive release, despatch, and returns, with a specific FEFO stock rotation requirement.

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