Accelerate Your Clinical Trials with Expert Oversight
TMClinical helps biotech startups and small sponsors run smarter, faster Phase 2/3 and medical device trials — without the overhead of a traditional CRO.
Our Expertise
Study Startup Optimization
Go from protocol to FPI faster with regulatory clarity, efficient site selection, and milestone planning.
CRO Oversight & Vendor Management
Vendor selection, bid defense, contracts, performance review, and hands-on sponsor-side oversight.
TMF Quality & Inspection Readiness
TMF QC, audit readiness, documentation standards, and GCP compliance guidance.
Medical Device Trial Consulting
Expert support for EU MDR/IVDR or FDA compliance, including CERs and PMS strategy.
What Our Clients Say
“TMClinical’s guidance was instrumental in the successful launch of our Phase 3 trial. Their attention to detail and proactive approach set them apart.”
– Dr. Jane Smith, CEO, Biotech Innovations
Frequently Asked Questions
Do you support Phase 1 trials?
We currently focus on Phase 2, Phase 3, and medical device trials. Phase 1 consulting may be offered through partners.
Where is your team based?
Our expert team operates remotely from Serbia, supporting global sponsors across the EU, UK, and US.
Can you help with TMF audits?
Yes. We provide TMF health checks, completeness QC, and readiness support tailored to inspection needs.
Do you offer CRO selection support?
Absolutely — we assist with vendor evaluation, bid support, and negotiation to ensure CRO alignment and efficiency.
Let’s Talk
Want expert help with your clinical trial startup, TMF quality, or vendor management?
Let’s discuss your goals and how TMClinical can support your next step.