Bring Life-Changing Pharmaceutical Therapies To
The 🇬🇧 Market The 🇬🇧 Market
We partner with pharmaceutical leaders to execute clinical trials with rapid enrollment, high retention, and uncompromising data quality.
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Bring Life-Changing Pharmaceutical Therapies To
Trusted Partners
For Sponsors
Clinical Trial Services
Expertise to handle any stage of the clinical research life-cycle.
Assisted trial design
Study Startup
Strategic consultation to optimize your study endpoints and methodology for maximum clinical impact.
Protocol writing
Study Startup
Developing scientifically rigorous and regulatory-compliant protocols tailored to your specific therapeutic area.
Site feasibility, selection, training and initiation
Study Startup
Identifying high-performing sites and ensuring teams are fully equipped to meet enrollment and safety targets.
IRB/ethics and regulatory submissions
Study Startup
Navigating complex global submission pathways to secure rapid approvals and maintain study timelines.
CTMS configuration and UAT
Study Startup
Setting up robust Clinical Trial Management Systems with thorough User Acceptance Testing for flawless operations.
Study plans
Study Startup
Crafting detailed operational roadmaps that align stakeholders and define clear paths to project milestones.
EMR databank querying
Patient Recruitment
Utilizing advanced Electronic Medical Record data to identify eligible participants with precision and speed.
Central digital advertising
Patient Recruitment
Running targeted multi-channel campaigns to reach diverse patient populations across digital platforms.
On-site patient recruitment
Patient Recruitment
Deploying specialist teams directly to clinical sites to facilitate face-to-face engagement and enrollment.
Study websites and marketing materials
Patient Recruitment
Designing patient-centric digital portals and high-quality printed materials to boost trial visibility.
Ready to discuss your clinical trial?
Connect with our experts to discuss how our integrated services can streamline your development timeline.
Protecting you & Safeguarding Volunteers
Bespoke Pharmacovigilance Solutions
Ensuring drug safety with a commitment to patient safety and regulatory excellence for small-to-mid size sponsors.
Adverse Event Reporting
- Streamlined reporting systems for adverse drug reactions (ADRs)
- End-to-end case processing and lifecycle management
- Real-time safety monitoring and signal identification
Regulatory Compliance
- Adherence to global pharmacovigilance regulations
- Customized solutions for local and international markets
- Audit preparation and inspection readiness
Literature Monitoring
- Comprehensive scientific literature surveillance
- Preparation of high-quality pharmacovigilance documentation
- Narrative writing, aggregate reports, and regulatory submissions
Risk Management Services
- Development and implementation of Risk Management Plans (RMPs)
- Periodic Safety Update Reports (PSURs) & Risk-Benefit Evaluation
- Proactive safety strategies for high-risk products
Signal Detection
- Advanced data mining and statistical safety analysis
- Early detection of emerging safety concerns
- Collaborative safety reviews with regulatory authorities
Inspection Readiness
- Inspection readiness training and internal audits
- Pharmacovigilance system master file (PSMF) support
- Mock inspections, interviews, and QPPV representation
Ready to secure your product's safety lifecycle?
Speak directly with our pharmacovigilance team to get a comprehensive review of your compliance gaps.
Contact Us
Visit Our Research Center
Our facility is easily accessible from the A5 and A422, offering dedicated parking for our volunteers and partners.
Primary Clinic Address
Unit F, Old Stratford Business Park, Falcon Drive, Old Stratford, Milton Keynes, MK19 6FG
Contact Reception
(+44) 1908 032992
cyprel@stemaxconsult.com
Timeline
The Volunteer Experience
Joining a trial gives you access to breakthrough medicines within a safety net of constant, expert medical attention.
1
Pre-Trial Phase
1–3 Days
Discovery & Pre-Screening
Confidential discussion about your condition and study goals. No cost or commitment required.
- ■ Review of medical history
- ■ Preliminary phone interview
- ■ Check against basic requirements
1 Visit
Informed Consent (ICF)
Critical meeting with the research doctor to review risks, benefits, and alternatives line-by-line.
- ■ Take document home to review
- ■ Ask questions freely
- ■ Sign only when ready
2–4 Weeks
Medical Screening
Comprehensive health check more detailed than a standard physical to ensure safety.
- ■ ECG, blood work, & vitals
- ■ Medication review
- ■ Diagnosis verification
2
Active Study Phase
Day 0
Randomization & Baseline
Assignment to a treatment group (often double-blind) and recording of baseline measurements.
- ■ Treatment assignment
- ■ Baseline health metrics
- ■ Receive study kit/diary
Months to Years
Treatment & Monitoring
Frequent clinic visits focused intensely on your specific condition and overall safety.
- ■ 24/7 medical team access
- ■ Real-time care adjustments
- ■ Travel reimbursement
3
Post-Trial Phase
4–12 Weeks
Safety Follow-Up
Monitoring after medication stops to ensure drug leaves system safely without delayed side effects.
- ■ Final labs & physical
- ■ Transition to GP
- ■ Share medical results
Optional
Long-Term Extension
Optional opportunity to roll over into an "Open Label Extension" to receive active medication.
- ■ Access to cutting-edge therapy
- ■ Continued cost-free care
- ■ Long-term safety contribution
Current Enrollment
Active Opportunities
Access cutting-edge pharmaceuticals, get paid for your time.
Enrolling
Chronic Obstructive Pulmonary Disease (COPD)
Clinical study for individuals aged 40-80 diagnosed with moderate to severe COPD and a history of smoking (10+ years).
Volunteer NowEnrolling
Lichen Simplex Chronicus (LSC)
Study for those experiencing moderate to severe skin itch affecting sleep despite 6+ months of medication.
Volunteer NowClosed
Covid-19 Vaccine Booster
Clinical trial study for adults and children over 12 regarding vaccine boosters.
Closed
Obsessive Compulsive Disorder (OCD)
Study for individuals aged 18-65 diagnosed with OCD for at least one year with inadequate relief from current treatments.
Testimonials
From Some Of Our Volunteers
"I was nervous about my first trial, but the medical team at Stemax was incredible. They talked me through every blood test and check-up, making me feel like a person, not just a data point."
David Richardson
Repeat Clinical Volunteer
"The flexibility of the outpatient visits was the deciding factor for me. I could book my appointments around my work shifts, and the clinic was always punctual and professional."
Samantha Reed
Asthma Study Participant
"It’s a great feeling knowing you’re helping to develop future medicines. The compensation for my time was fair and paid promptly, which was a nice bonus for helping a good cause."
Marcus Thompson
Healthy Volunteer
"The level of care I received at Stemax was better than my regular GP surgery. The screening process was so thorough that I actually learned a lot more about my own general health."
Elena Petrova
Phase II Trial Participant
"Clear communication is everything. From the initial phone call to the final follow-up, the Stemax staff kept me informed about what to expect. There were no surprises and no stress."
Jordan Hayes
Clinical Research Volunteer
"I’ve participated in two trials here now. The facility is modern, the nurses are friendly, and the whole process is incredibly well-organized. I’d recommend it to anyone curious about research."
Chloe Whitworth
Healthy Volunteer
Frequently Asked Questions
Common Questions & Patient Rights
Stepping into clinical research is a unique opportunity to access breakthrough medicines within a safety net of constant expert monitoring. We ensure you feel confident, seen, and protected at every turn.
A clinical trial is a research study conducted with human participants to evaluate the safety and effectiveness of new medical treatments, drugs, or devices. These studies are essential for bringing new medical advancements to the public.
Need Assistance?
All related office visits, medical evaluations, and study medication are provided at no charge. Financial compensation for time and travel may be provided.
Contact Us
Visit Our Research Center
Our facility is easily accessible from the A5 and A422, offering dedicated parking for our volunteers and partners.
Primary Clinic Address
Unit F, Old Stratford Business Park, Falcon Drive, Old Stratford, Milton Keynes, MK19 6FG
Contact Reception
(+44) 1908 032992
cyprel@stemaxconsult.com