TrialTrust Global Clinical Trial Document Writing & Review Services for Afghanistan
Regulatory-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 successfully supported 330+ clinical trial documentation projects for clients across Asia, Middle East, Africa, Europe, 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 data, strong clinical justification, and internationally aligned regulatory documentation suitable for Afghanistan-linked and global submissions.
Our Services for Clients in Afghanistan
🧪 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 & authority-ready formats
📊 Clinical Study Report (CSR) Writing
Full Clinical Study Reports compliant with ICH E3
Clinical data interpretation & 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 scientific & regulatory review of CT documents
Gap assessment against ICH-GCP, WHO, USFDA, EMA & international MOH expectations
Scientific consistency & data integrity checks
🛂 Post-Submission Query Handling
Responses to Health Authorities, Ethics Committees & International Review Bodies
Scientific rebuttals & clarifications
Deficiency letter responses
Regulatory follow-up support until closure
Industries We Serve for Afghanistan Programs
Pharmaceutical Finished Dosage Forms
Nutraceuticals & Dietary Supplements
Herbal & Botanical Products
Functional Foods & Medical Nutrition
Generic & Branded Products
Export-oriented & donor-supported clinical programs
International Regulatory Alignment
Our Clinical Trial documentation is prepared in alignment with:
ICH-GCP (E6)
ICH E3 – Clinical Study Reports
WHO Guidelines
USFDA
EMA
International MOH & Ethics Committee requirements
Country- and project-specific regulatory formats
Why Clients Working in Afghanistan Choose TrialTrust
✅ 330+ Clinical Trial Documents Delivered Globally
✅ Experienced Clinical & Regulatory Experts
✅ Strong Pharma & Nutraceutical Expertise
✅ Authority-Acceptable & Inspection-Ready Documentation
✅ End-to-End Post-Submission Support
✅ Confidential, Accurate & Timeline-Driven Execution
Our Experience Footprint
330+ products supported worldwide
Clients across Asia, Middle East, Africa, Europe & LATAM
Experience with emerging, humanitarian, and export-driven clinical programs
Support for local, regional, and international regulatory submissions
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 managed under strict confidentiality agreements, with robust quality control, version control, and data integrity practices, ensuring regulatory confidence and global acceptance.
Contact TrialTrust – Afghanistan Programs
Looking for reliable, internationally compliant Clinical Trial documentation support for your pharmaceutical or nutraceutical product linked to Afghanistan?
Partner with TrialTrust — where clinical science meets regulatory excellence.
📩 Contact us today to discuss your Clinical Trial documentation requirements for Afghanistan.