TrialTrust Global Clinical Trial Document Writing & Review Services in Cyprus
egulatory-Compliant | Authority-Ready | Globally Trusted
Who We Are
TrialTrust, the scientific arm of Zoesoe Exports Pvt. Ltd., provides end-to-end Clinical Trial (CT) Document Writing and Review Services for pharmaceutical and nutraceutical products across regulated and semi-regulated global markets.
Since 2008, we have delivered 330+ clinical trial documentation projects for sponsors, CROs, and manufacturers across Europe, Asia, the Middle East, Africa, and LATAM.
We specialize in the preparation, review, and post-submission support of Clinical Trial Protocols and Clinical Study Reports (CSRs), supported by complete scientific datasets, robust clinical justification, and EU-aligned regulatory documentation suitable for Cyprus and multinational EU submissions.
Our Services for Clients in Cyprus
🧪 Clinical Trial Protocol Writing
Phase I–IV, BA/BE, Pilot & Pivotal studies
Pharmaceutical & Nutraceutical products
Study design, objectives, endpoints & statistical rationale
Inclusion/exclusion criteria & risk–benefit assessment
Ethics Committee & EU-authority-ready formats
📊 Clinical Study Report (CSR) Writing
Full Clinical Study Reports compliant with ICH E3 & EU CTR expectations
Data interpretation & clinical conclusions
Tables, Listings & Figures (TLFs)
Safety & efficacy evaluation
Investigator and site data integration
📁 Backup & Supporting Documentation
Investigator’s Brochure (IB)
Informed Consent Forms (ICF)
Case Report Form (CRF) review support
Statistical Analysis Plan (SAP)
Literature review & clinical justification documents
🔄 Document Review & Gap Assessment
Independent technical & regulatory review of CT documents
Gap assessment against ICH-GCP, EU CTR (536/2014), EMA & Cyprus MOH requirements
Scientific consistency & data integrity checks
🛂 Post-Submission Query Handling
Responses to Cyprus Ministry of Health, National Ethics Committees & EMA
Scientific rebuttals & clarifications
Deficiency letter responses
Regulatory follow-up support until closure
Industries We Serve in Cyprus
Pharmaceutical Finished Dosage Forms
Generic & Branded Medicines
Nutraceuticals & Food Supplements
Herbal & Botanical Products
Functional Foods & Medical Nutrition
EU export-oriented clinical programs
Cyprus & EU Regulatory Alignment
Our Clinical Trial documentation is prepared in alignment with:
ICH-GCP (E6)
ICH E3 – Clinical Study Reports
EU Clinical Trial Regulation (EU CTR 536/2014)
EMA guidelines
Cyprus Ministry of Health requirements
WHO Guidelines
Country-specific Ethics Committee formats
Why Companies in Cyprus Choose TrialTrust
✅ 330+ Clinical Trial Documents Delivered Worldwide
✅ Experienced EU-Focused Clinical & Regulatory Experts
✅ Strong Pharma & Nutraceutical Specialization
✅ Authority-Acceptable & Inspection-Ready Documentation
✅ End-to-End Post-Submission Support
✅ Confidential, Accurate & Timeline-Driven Execution
Our Experience Footprint
330+ products supported globally
Clients across EU, Asia, Middle East & Africa
Expertise in EU CTR submissions via CTIS
Support for Cyprus-only, multi-country EU & global filings
Our Working Approach
Requirement Understanding & Scope Finalization
Regulatory Strategy & Study Design Alignment
Clinical Document Preparation / Review
Internal Scientific & Quality Review
Client Review & Finalization
Post-Submission Authority Query Handling
Confidentiality & Quality Commitment
All projects are handled under strict confidentiality agreements, with strong quality management, version control, and data integrity practices, ensuring regulatory confidence and EU acceptance.
Contact TrialTrust in Cyprus
Looking for reliable, EU-compliant Clinical Trial documentation support for your pharmaceutical or nutraceutical product?
Partner with TrialTrust — where clinical science meets regulatory excellence.
📩 Contact us today to discuss your Clinical Trial documentation needs in Cyprus.