Experience the benefits of conducting your next study in Central or Eastern Europe
Support From Start to Finish at Every Stage of Your Study
Free feasibility report
Start up
Regulatory submissions and site activation
Study conduct
Patient enrollment and data collection
Data analysis
Statistical analysis and reporting
Regulatory submissions
Dossier preparation and filling
Post submission
Authority queries and follow-up
Study Success
Approval and market success
Key Advantages of Choosing a CRO in Europe
Palleos delivers premium CRO services right in the heart of Europe. Operating across Central and Eastern Europe, we combine local expertise with global standards. When you choose Palleos, you gain a partner who knows the local landscape, speaks the language, and delivers CRO services that keep your study on track.
Cost Efficiency
Lower operational costs vs. Western Europe / US
World-class Enrollment
Patients enrolled by Palleos while preserving budgets and timelines
Only Target Participants
Research sites with low screen failure and high naïve patient recruitment.
Quality & Compliance
All sites comply with ICH-GCP and EU CTR standards
Realistic Timelines
We don’t promise what can’t be delivered: we prefer to be realistic rather than over-optimistic.
Transparent Budgeting
We deliver a very thorough and structured budget grid with detailed justification
Seamless communication
Efficient project management and coordinated sponsor experience
16+ Years of Expertise
Projects in 29 therapeutic areas under our belt
Full-Service CRO Expertises for Phase I-IV & BE
We provide a full range of high-quality clinical trial services for Phase I-IV and BE studies. We offer both full-service clinical study engagements and standalone CRO services tailored to your needs.
Clinical Study Design
Efficient project management and coordinated sponsor experience
Medical Writing
Clinical documents, reports and publications
Consulting & Regulatory Support
Strategic regulatory guidance across EU market
Drug Safety & Pharmacovigilance
Safety monitoring and adverse event management
Project Management & Monitoring
End-to-end project oversight and site monitoring
Clinical Data Management
Data collection, cleaning, and quality assurance
Biostatistics
Statistical analysis plans and data interpretation
Marketing Authorization
Regulatory dossier preparation and submission
GMP Inspection Support
Preparation and support for GMP inspections
Clinical Supply Services and Logistics
Drug supply chain management and distribution
We are proud to offer expertise in 29 therapeutic areas
Our extensive track record of managing studies gives your drug the best chance to succeed
Trusted by Sponsors Across the Globe
Partner with Palleos – your trusted CRO in Europe
Whether you need full CRO services or support at a specific stage, our team is ready to help. From free feasibility to post-submission, we are an email or a phone call away.
