TrialTrust – Global Clinical Trial Document Writing & Review Services for Panama
Regulatory-Compliant | Authority-Ready | Globally Trusted
Clinical Trial Documentation Support for Panama & International Submissions
TrialTrust, the scientific arm of Zoesoe Exports Pvt. Ltd., provides end-to-end Clinical Trial (CT) Document Writing, Review, and Regulatory Support Services for Panama-based pharmaceutical, nutraceutical, biotechnology, and healthcare companies, as well as organizations conducting or submitting clinical programs across Central America, LATAM, and global markets.
We support local submissions to the Panamanian health authority (Ministry of Health – MINSA) and export-oriented clinical programs, ensuring documentation aligned with national regulations and harmonized with international clinical research standards.
Since 2008, TrialTrust has successfully delivered 330+ clinical trial documentation projects for clients across LATAM, North America, Europe, Asia, Middle East, and Africa.
Who We Are
TrialTrust is a specialized clinical and regulatory documentation partner supporting:
Panamanian pharmaceutical manufacturers and importers
Nutraceutical, dietary supplement & wellness product companies
Biotechnology & medical nutrition developers
CROs, research institutions & export-focused product owners
We specialize in the preparation, independent review, and post-submission query handling of:
Clinical Trial Protocols
Clinical Study Reports (CSR)
All documentation is supported by complete backup data, strong scientific justification, and authority-aligned formats, ensuring inspection-ready and regulator-acceptable submissions.
What We Do
We provide complete lifecycle support for Clinical Trial documentation — from protocol development and ethics submission to final report submission and regulatory authority query closure.
Our Core Clinical Trial Services
🧪 Clinical Trial Protocol Writing
Clinical Trial Protocols (Phase I–IV, BA/BE, Pilot & Pivotal studies)
Protocols for Pharmaceutical, Biotech & Nutraceutical products
Study design, objectives, endpoints & statistical rationale
Inclusion/exclusion criteria & risk–benefit assessment
Ethics Committee & MINSA-ready formats
Alignment with ICH-GCP and Panamanian regulatory expectations
📊 Clinical Study Report (CSR) Writing
Full ICH E3-compliant Clinical Study Reports
Clinical data interpretation & conclusions
Tables, Listings & Figures (TLFs)
Safety & efficacy evaluation
Investigator, site & subject data integration
Suitable for Panama, LATAM, FDA, EMA, and global submissions
📁 Backup & Supporting Documentation
Investigator’s Brochure (IB)
Informed Consent Forms (ICF)
Case Report Form (CRF) review support
Statistical Analysis Plan (SAP)
Literature reviews & clinical justification documents
🔄 Document Review & Gap Assessment
Independent technical & regulatory review of CT documents
Gap assessment against ICH-GCP, WHO, PAHO, FDA, EMA, and Panamanian regulatory requirements
Scientific consistency, traceability & data integrity checks
🛂 Post-Submission Query Handling
MINSA / Ethics Committee query responses
Scientific rebuttals & regulatory clarifications
Deficiency letter responses
Follow-up support until regulatory closure
Industries We Serve
Pharmaceutical Finished Dosage Forms
Biotechnology & Biological Products
Nutraceuticals & Dietary Supplements
Herbal & Botanical Products
Functional Foods & Medical Nutrition
Export-oriented Clinical Programs
Global Regulatory Alignment
Our Clinical Trial documentation is prepared in alignment with:
ICH-GCP (E6)
ICH E3 – Clinical Study Reports
WHO & PAHO Guidelines
USFDA
EMA
Central American & LATAM MOH requirements
Country-specific Ethics Committee formats
Why Choose TrialTrust
✅ 330+ Clinical Trial Documents Delivered Globally
✅ Dedicated Clinical & Regulatory Experts
✅ Pharma, Biotech & Nutraceutical Specialization
✅ Authority-Acceptable & Inspection-Ready Documentation
✅ Strong Post-Submission Regulatory Support
✅ Confidential, Accurate & Timeline-Driven Execution
Our Experience Footprint
330+ products supported globally
Clients across LATAM, North America, Europe, Asia, Middle East & Africa
Experience in new products, line extensions & lifecycle management
Support for local registrations and international submissions
Our Working Approach
Requirement Understanding & Scope Finalization
Regulatory Strategy & Study Design Alignment
Clinical Document Preparation / Review
Internal Quality & Scientific Review
Client Review & Finalization
Post-Submission Authority Query Handling
Confidentiality & Quality Commitment
All projects are handled under strict confidentiality agreements, supported by robust quality control systems, version control, and data integrity practices, ensuring regulatory confidence and global acceptance.