Clinical Trial Excellence: GCP Audits, ClinOps Support & On Demand Training
At CRDE, we combine quality-focused audits, hands-on clinical-operations support and bite-size online training to keep your studies compliant, efficient and inspection-ready.
Get StartedWhat is it we do?
CRDE empowers life-science teams to hit their study milestones by combining end-to-end strategic trial management, lean operational workflows and quality oversight.
We blend audit-grade rigor with hands-on clinical operations and disciplined vendor oversight.
Integrity
We hold ourselves to ICH GCP and your SOPs without compromise—transparent, evidence based and accountable in every interaction.
Innovation
We adopt smarter tools and risk-based methods to streamline work, surface issues early and keep you a step ahead of timelines.
Client-Centric
Your objectives set our course. We tailor engagement models, KPIs and communication to fit your team, not the other way round.
Collaboration
We act as an extension of your organization, sharing knowledge to solve problems fast and keep momentum high.
Partner dedicated to your clinical trial’s success
Clinical trials run on tight timelines, strict regulations and a maze of outsourced partners—one weak link can derail the whole study. Our mix of audits, trainings, operational management and vendor oversight closes those gaps, giving you real control over quality, cost and deadlines. Instead of reacting to findings or missed milestones, you see risks early and act decisively. The result: inspection-ready studies that finish on time and protect both patients and your budget.
Join the success stories
“Their team helped us navigate a challenging market with confidence. Truly invaluable.”
David
“Exceptional service and support!”
Emma
“Incredibly professional and effective. They took our business to the next level.”
Karen
“Their strategic guidance was a game-changer for our company. We’re now positioned for long-term success.”
Jonathan
“The insights from CRDE transformed our study strategy. Highly recommend!”
Sarah
“Thanks to their expertise, we streamlined our operations and saw immediate results.”
Michael
Drive your studyforward with our services
From GCP audits and compliance checks to hands-on clinical operations management, CRO/vendor oversight and self paced e-trainings, we cover the full spectrum of your trial needs.
Get Started NowFrequently asked questions
We conduct risk-based audits of sites, TMFs, processes and vendors against ICH GCP, regulations and your SOPs. You get a clear report with prioritized findings, CAPA recommendations and optional follow-up support to ensure fixes actually stick.
Outsourcing doesn’t remove sponsor responsibilities. We set up oversight plans, KPIs and governance routines, review deliverables and escalate early, so you keep control of quality, timelines and budget without micromanaging day to day.
Yes. All e-trainings are fully self-paced and accessible 24/7.
Absolutely. We can embed as an extension of your team to troubleshoot enrollment, shore up timelines or manage vendors. After a short scoping call, we usually mobilize within days and tailor our involvement to your specific gaps.
Clinical Trial Know-How, Delivered When You Need It.
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