As AI regulation accelerates globally, 360 Clinical Research Consultancy provides expert independent auditing to ensure your AI systems meet regulatory requirements and the highest ethical standards.
Talk to Our TeamOur auditing processes are ISO compliant, ensuring internationally recognised standards of quality, rigour, and consistency.
We operate with complete independence from AI vendors and developers, giving you an unbiased, objective assessment.
Deep expertise in the EU AI Act and GDPR, helping organisations navigate the regulatory landscape with confidence.
We provide comprehensive auditing across all dimensions of AI systems — from technical model reviews to governance frameworks and regulatory compliance.
Identify, evaluate and prioritise risks within your AI systems, including safety, security, privacy, and ethical risks across the full system lifecycle.
Technical review of AI models for bias, accuracy, reliability, and robustness across diverse populations and deployment scenarios.
Ensure compliance with the EU AI Act, GDPR, and emerging AI regulations across jurisdictions, with gap analysis and remediation roadmaps.
Assess the explainability and documentation of AI decision-making processes to satisfy stakeholders, customers, and regulators.
Detect and address discriminatory patterns in AI outputs to ensure fair and equitable treatment across all user groups and demographics.
Develop and assess governance frameworks, policies, and oversight mechanisms that enable responsible and accountable AI deployment.
“360 Clinical Research Consultancy gave us the clarity and confidence to deploy our AI system knowing it meets both regulatory expectations and our own ethical standards.”
Chief Technology Officer
Financial Services Organisation
At 360 Clinical Research Consultancy, we believe that trustworthy AI starts with rigorous, independent auditing. Our team brings deep technical expertise and regulatory knowledge to every engagement, helping organisations deploy AI systems with confidence.
Start Your AI AuditTalk to our team today about how 360 Clinical Research Consultancy can help your organisation achieve and maintain regulatory compliance.
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Welcome to the March 2026 edition of the 360 Clinical Research Consultancy Insights! In this issue, March Becomes the Implementation Month: What the UK’s Countdown Webinar Revealed
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Welcome to the February 2026 edition of the 360 Clinical Research Consultancy Insights! In this issue, FDA’s One-Trial Default Changes the Conversation: What February 2026 Means for Drug Development Strategy.
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Welcome to the January 2026 edition of the 360 Clinical Research Consultancy Insights! In this issue, UK Clinical Trial Competitiveness Becomes a 2026 Priority: Faster Assessments, Agile Regulation, and What It Means for Sponsors
10 Jan 2026
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