TrialTrust Global
Clinical Trial Document Writing & Review Services – Israel
MOH-Aligned | IRB/EC-Ready | Globally Trusted
Trusted Clinical Trial Documentation Partner for Israel
TrialTrust, a scientific arm of Zoesoe Exports Pvt. Ltd., provides end-to-end Clinical Trial (CT) Document Writing and Review Services for pharmaceutical, biotechnology, and nutraceutical companies conducting clinical trials in Israel.
Israel is a recognized clinical research hub in the Middle East, selected for Phase I–IV, bioequivalence, oncology, CNS, cardiovascular, and vaccine studies, regulated by the Israeli Ministry of Health (MOH) and local Institutional Review Boards (IRBs / Ethics Committees). TrialTrust supports sponsors and CROs with scientifically robust, authority-ready documentation, aligned with Israeli and global standards.
Since 2008, TrialTrust has delivered 330+ clinical trial documentation projects for clients across Europe, Asia, Middle East, Africa, and LATAM.
Who We Serve in Israel
We work with:
Israeli & global pharmaceutical companies
Biotechnology & biosimilar developers
CROs conducting trials in Israel
Generic & branded product manufacturers
Nutraceutical & dietary supplement companies
Sponsors conducting local or multi-country clinical trials
Whether your study is Israel-only or part of a global MRCT program, we ensure full MOH and IRB/Ethics Committee compliance.
Our Clinical Trial Documentation Services
🧪 Clinical Trial Protocol Writing
Regulatory-ready Clinical Trial Protocols aligned with Israeli standards:
Phase I–IV Clinical Trial Protocols
BA/BE, Pilot & Pivotal study protocols
Pharma, Biotech & Nutraceutical product protocols
Study design, objectives, endpoints & statistical rationale
Inclusion/exclusion criteria & risk–benefit assessment
MOH & IRB-aligned formats
📊 Clinical Study Report (CSR) Writing
Comprehensive ICH E3-compliant Clinical Study Reports suitable for Israel and global submissions:
End-to-end CSR writing & medical interpretation
Safety & efficacy evaluation
Tables, Listings & Figures (TLFs)
Investigator & site data integration
Clear regulatory-ready clinical conclusions
📁 Backup & Supporting Documentation
Complete supporting documentation required for MOH, IRBs, and global regulatory submissions:
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 scientific and regulatory review services:
Gap assessment against:
Israeli MOH requirements
IRB / Ethics Committee standards
ICH-GCP (E6)
ICH E3 – Clinical Study Reports
EMA, USFDA & WHO guidelines
Scientific consistency & data integrity checks
🛂 Post-Submission Query Handling
Complete regulatory follow-up support until closure:
MOH & IRB query responses
Scientific rebuttals & regulatory clarifications
Deficiency response support
Ongoing authority follow-up until approval
Industries We Support in Israel
Innovative & Generic Pharmaceuticals
Biotechnology & Biosimilars
Oncology, CNS, Cardiovascular & Vaccine Products
Nutraceuticals & Dietary Supplements
Herbal & Botanical Products
Export-driven Israeli & global clinical programs
Regulatory Alignment & Compliance
All clinical trial documents are prepared in alignment with:
Israeli Ministry of Health (MOH)
Institutional Review Boards / Ethics Committees
ICH-GCP (E6)
ICH E3 – Clinical Study Reports
EMA, WHO & USFDA guidelines
Why Israel-Focused Companies Choose TrialTrust
✅ 330+ Clinical Trial Documents Delivered Globally
✅ Strong Experience Supporting Israeli & International Clinical Trials
✅ Expertise in Pharma, Biotech & Nutraceutical Products
✅ MOH & IRB-Aligned Documentation
✅ Reliable Post-Submission & Regulatory Support
✅ Confidential, Accurate & Timeline-Driven Execution
Our Experience Footprint
330+ products supported worldwide
Clients across Europe, Asia, Middle East, Africa & LATAM
Experience in MRCTs, Israel-only, and global lifecycle management
Support for MOH approvals and international submissions
Our Working Approach
Requirement Understanding & Israel / Global Scope Finalization
MOH & IRB/Ethics Committee Strategy Alignment
Clinical Document Writing / Review
Internal Quality & Scientific Review
Client Review & Finalization
Post-Submission Authority Query Handling
Confidentiality & Quality Commitment
All Israel-related projects are handled under strict confidentiality agreements, supported by:
Robust quality control systems
Version control & audit readiness
Scientific accuracy & data integrity assurance
Ensuring regulatory confidence and global acceptance.
Get in Touch – Israel Clinical Trial Support
Looking for MOH-aligned, Israel-compliant Clinical Trial documentation for your pharmaceutical, biotech, or nutraceutical product in Israel?
Partner with TrialTrust — where clinical science meets regulatory excellence.
📩 Contact us today to discuss your Clinical Trial documentation needs