News & Insights
Compliance news,
guidance & product updates
Practical articles on standards, audits and the Cornerstone platform — written by the team that implements them.
COS-GMP
2 Jul 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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ISO 22716
2 Jul 2026 · 4 min read
ISO 22716 Section 6 Explained: Raw Materials and Packaging Materials
ISO 22716 Section 6 covers purchasing, receipt, identification, storage, and release of raw materials and packaging. Here is where supplier approval becomes a GMP requirement.
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COS-GMP
1 Jul 2026 · 4 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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ISO 22716
1 Jul 2026 · 3 min read
ISO 22716 Section 5 Explained: Equipment Requirements for Cosmetics GMP
ISO 22716 Section 5 covers equipment design, calibration, cleaning, and maintenance. Here is what manufacturers need in place and why calibration gets flagged so often.
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ISO 22716
30 Jun 2026 · 3 min read
ISO 22716 Section 4 Explained: Premises Requirements for Cosmetics GMP
ISO 22716 Section 4 sets out requirements for facility layout, flow, cleaning, and pest control. Here is what auditors actually check on the floor.
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COS-GMP
30 Jun 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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ISO 22716
29 Jun 2026 · 3 min read
ISO 22716 Section 3 Explained: Personnel Requirements for Cosmetics GMP
ISO 22716 Section 3 covers organisation, training, and hygiene for personnel working in cosmetics GMP environments. Here is what it actually requires.
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COS-GMP
29 Jun 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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Compliance Insights
19 Jun 2026 · 4 min read
ZenQMS Alternative for UK Food and Cosmetics Manufacturers: What to Look For
ZenQMS is built for medical device and pharma quality management. UK food and cosmetics manufacturers researching alternatives should check these specific gaps first.
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Compliance Insights
18 Jun 2026 · 4 min read
Supplier Approval Workflows: What Most Manufacturers Get Wrong
Supplier approval is often treated as a one-time gate rather than an ongoing process. Here is what a proper supplier approval workflow actually requires.
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Compliance Insights
17 Jun 2026 · 4 min read
What Is CAPA and Why Does It Matter More Than Auditors Let On
CAPA stands for Corrective and Preventive Action. Here is what it actually means in practice, and why poorly run CAPA processes are one of the most common audit findings.
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Compliance Insights
16 Jun 2026 · 4 min read
Why Per-User QMS Pricing Quietly Becomes a Problem as You Grow
Per-seat licensing looks manageable at evaluation time and becomes a real constraint later. Here is the actual mechanism by which that happens.
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Compliance Insights
12 Jun 2026 · 4 min read
Looking for a Qualio Alternative? What Cosmetics Manufacturers Should Check First
Qualio is built for life sciences. If you manufacture cosmetics or food products, here is what to actually check before choosing an alternative.
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