Deep dives, practical guides, and incident analyses from engineers who build Safeguard. No fluff, no vendor FUD — just what you need to ship secure software.
Vendors receiving student records may use them only for the disclosed purpose and may not redisclose them. How that applies to subprocessors and analytics.
FDA issued a final premarket cybersecurity guidance for medical devices in February 2026. What the page says, what it replaces, how to read section 524B.
When you deprioritize a finding because it is not reachable, buyers and auditors want evidence. What to record, how to word it, and what to avoid claiming.
A predictable evidence folder cuts audit questions. Use one folder per control, dated file names and a short index so anyone can find a record fast.
What the EU Instant Payments Regulation requires for payee verification, the match outcomes to design for, the dates, and the liability rule.
Without an adequacy decision, GDPR transfers need safeguards such as standard clauses or BCRs. What the options are and where the EU US framework stands.
What the recitals of Regulation (EU) 2023/1230 say about malicious third parties, cybersecurity schemes and self-evolving machine learning in safety.
Articles 11 and 72 require high-risk AI providers to keep Annex IV documentation up to date and to monitor performance after release. A practical outline.
The EU AI Act sorts AI into four tiers: prohibited, high-risk, transparency risk and minimal. Examples of each tier and the duties that follow from them.
Weekly insights on software supply chain security, delivered to your inbox.
Your first fix PR is minutes away.
No sales call required, even your agent can complete the purchase over MCP.
