The Complete Auditing Solution
360 Clinical Research Consultancy (CRC) is dedicated to compliance consultancy of your Clinical Research and Post Marketing needs.
Auditing Solutions
From clinical trial compliance to cutting-edge AI system auditing, 360 CRC provides specialised services tailored to your organisational needs.
AI Audits
As AI systems become embedded in regulated environments, independent audit and validation of AI models has never been more critical. The 360 CRC AI audit service ensures your systems meet regulatory expectations.
Learn MoreClinical Research Auditing
Comprehensive auditing services covering pharmacovigilance, investigator sites, data integrity, risk management, inspection readiness, and more. Serving clients from startup biotech to established multinationals.
Learn MoreWhy Choose 360 Clinical Research Consultancy (CRC)?
360 CRC combines deep regulatory expertise with a partnership approach to deliver measurable outcomes for your compliance programme.
Deep Expertise
Bringing decades of combined experience in GxP auditing, regulatory affairs, and quality management across global pharmaceutical and medical device organisations.
Global Reach
Supporting clients across Europe, North America, and beyond, with an understanding of ICH guidelines, FDA, EMA, and HPRA regulatory frameworks.
Compliance Assured
Audit methodologies are rooted in current GxP expectations, ensuring your organisation is always prepared for regulatory inspections.
True Partnership
Working alongside your team, not just as auditors but as trusted advisers — helping you understand findings and implement sustainable corrective actions.
Results Focused
Every engagement is measured against clear outcomes. Helping organisations reduce risk, improve quality systems, and emerge stronger from regulatory scrutiny.
Tailored Approach
No two audits are the same. 360 CRC tailors the scope, methodology, and reporting to address the specific needs and risk profile of your organisation.
“360 Clinical Research Consultancy gave us the confidence to face our regulatory inspection. Their expertise and thoroughness gave us complete clarity on our compliance position.”
Head of Quality Assurance
European Biotech Company
Ready 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
5 min read
A sponsor company running a suite of early access programs discovered critical gaps in oversight, safety reporting, and HCP accountability — prompting a structured audit-led intervention.
30 Aug 2025
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12 min read
A start-up biotech company developing an innovative investigational drug product faced growing challenges around oversight, data integrity, and inspection readiness as it moved into later phase development.
24 Apr 2025
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