The Complete Clinical Research Auditing Solution
Dedicated to compliance consultancy of your Clinical Research and Post Marketing needs.
Start Your Clinical AuditA passion for Clinical Research Auditing
A comprehensive suite of professional services catering to a diverse clientele, from startup biotech to established multinationals — with a focus on quality, compliance, and inspection readiness.
Risk Management
Risk analysis and planning, risk management and remediation, corrective and preventative action (CAPA), and proactive risk mitigation strategies.
Auditing
Pharmacovigilance (clinical trial and post-marketing), supplier, investigator site, data (clinical study reports, statistics, CTD) and system audits.
Inspection Planning and Management
Comprehensive inspection preparation including mock inspections, sponsor oversight support, and ongoing inspection management.
Consulting
Quality Management System (QMS) development including controlled documents, SOPs, and full electronic QMS design and implementation.
Training
GxP training programmes, inspection preparation training, CAPA management training, and bespoke workshops for clinical teams.
For Cause
Expert management of for cause investigations, root cause analysis, regulatory response support, and CAPA implementation.
“360 CRC has saved us hours of work and has unlocked insights we never thought possible.”
Malcom Donoghue
CEO, BioTech Startup
Our Commitment to Quality
At 360 Clinical Research Consultancy, quality is not a checkbox — it is the foundation of everything we do. 360 CRC brings deep clinical research expertise and regulatory knowledge to every engagement, helping organisations achieve lasting compliance and inspection confidence.
Start Your Clinical AuditReady to strengthen your compliance?
Talk to 360 CRC today about how 360 Clinical Research Consultancy can help your organisation achieve and maintain regulatory compliance.
Get in TouchLatest Posts
12 min read
Welcome to the May 2026 edition of the 360 Clinical Research Consultancy Insights! In this issue, FDA Inspection Reach, Real-Time Trials, and Modern Evidence Design.
08 May 2026
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12 min read
Welcome to the April 2026 edition of the 360 Clinical Research Consultancy Insights! In this issue, The New UK Clinical Trials Regulations Are Live: What April 2026 Changed in Practice
10 Apr 2026
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12 min read
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
10 Mar 2026
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