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COS-GMP
Featured 06.07.2026 · 3 min read

COS-GMP Section 10 Explained: Production

COS-GMP Section 10 covers bulk manufacturing and filling and packaging operations, using the term traceability code rather than batch number throughout.

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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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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 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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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 3 Explained: Documentation COS-GMP

29.06.2026 · 3 min read

COS-GMP Section 3 Explained: Documentation

COS-GMP Section 3 covers document and record control, including specific rules on electronic documentation that go further than older cosmetics GMP standards.

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COS-GMP Section 4 Explained: Risk Control COS-GMP

30.06.2026 · 3 min read

COS-GMP Section 4 Explained: Risk Control

COS-GMP Section 4 introduces a formal HARA process and detailed contamination controls that go well beyond what ISO 22716 requires explicitly.

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COS-GMP Section 5 Explained: GMP Safety and Quality Management COS-GMP

01.07.2026 · 3 min read

COS-GMP Section 5 Explained: GMP Safety and Quality Management

COS-GMP Section 5 is the standard's largest section, covering nonconformances, CAPA, concessions, traceability, complaints, recalls, procurement, change control, and internal audits.

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COS-GMP Section 6 Explained: Personnel COS-GMP

02.07.2026 · 3 min read

COS-GMP Section 6 Explained: Personnel

COS-GMP Section 6 covers personnel requirements, with an explicit Senior Management commitment clause that goes further than ISO 22716's equivalent.

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COS-GMP Section 7 Explained: Premises and Site Standards COS-GMP

03.07.2026 · 3 min read

COS-GMP Section 7 Explained: Premises and Site Standards

COS-GMP Section 7 covers premises requirements with more specific detail than ISO 22716 on signage, staff facilities, and documented site plans.

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COS-GMP Section 8 Explained: Equipment COS-GMP

04.07.2026 · 3 min read

COS-GMP Section 8 Explained: Equipment

COS-GMP Section 8 covers equipment design, new equipment acceptance, calibration, and cleaning — with a distinct factory acceptance testing concept not explicit in ISO 22716.

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COS-GMP Section 9 Explained: Purchasing and Goods Intake COS-GMP

05.07.2026 · 3 min read

COS-GMP Section 9 Explained: Purchasing and Goods Intake

COS-GMP Section 9 covers goods intake and release, with a distinct sub-section on water used as a stock item.

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