The Complete Auditing Solution
Here at 360 Clinical Research Consultancy we are dedicated to compliance consultancy of your Clinical Research and Post Marketing needs.
Our Auditing Solutions
From clinical trial compliance to cutting-edge AI system auditing, we provide specialised services tailored to your organisation's needs.
AI Audits
As AI systems become embedded in regulated environments, independent audit and validation of AI models has never been more critical. Our 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?
We combine deep regulatory expertise with a partnership approach to deliver measurable outcomes for your compliance programme.
Deep Expertise
Our team brings decades of combined experience in GxP auditing, regulatory affairs, and quality management across global pharmaceutical and medical device organisations.
Global Reach
We support clients across Europe, North America, and beyond, with an understanding of ICH guidelines, FDA, EMA, and HPRA regulatory frameworks.
Compliance Assured
Our audit methodologies are rooted in current GxP expectations, ensuring your organisation is always prepared for regulatory inspections.
True Partnership
We work 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. We help organisations reduce risk, improve quality systems, and emerge stronger from regulatory scrutiny.
Tailored Approach
No two audits are the same. We tailor our 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 our team 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 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
Read More →
12 min read
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.
10 Feb 2026
Read More →
12 min read
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
Read More →