TrialTrust – Global Clinical Trial Document Writing & Review Services

For Pharmaceutical & Nutraceutical Companies in Côte d’Ivoire

• Regulatory-Compliant | Authority-Ready | Globally Trusted

  Who We Are

  TrialTrust, a scientific arm of Zoesoe Exports Pvt. Ltd., provides end-to-end Clinical Trial (CT) Document Writing and Review Services for pharmaceutical and nutraceutical products, supporting organizations in Côte d’Ivoire (Ivory Coast) for local regulatory submissions and international market approvals.

  Since 2008, TrialTrust has successfully delivered 330+ clinical trial documentation projects across Asia, Middle East, Africa, Europe, and LATAM, ensuring scientific rigor, regulatory compliance, and authority acceptance.

  We specialize in the preparation, independent review, and post-submission query handling of Clinical Trial Protocols and Clinical Study Reports, supported by complete backup data, strong scientific justifications, and regulator-aligned documentation.

  What We Do

  We provide complete lifecycle support for Clinical Trial documentation—from protocol development to final report submission and post-submission authority / ethics committee query resolution—tailored for sponsors, manufacturers, MAHs, and exporters operating in or from Côte d’Ivoire.

  Our Core Clinical Trial Services

  🧪 Clinical Trial Protocol Writing

  • Clinical Trial Protocols (Phase I–IV, BA/BE, Pilot & Pivotal studies)

  • Protocols for Pharmaceutical & Nutraceutical products

  • Study design, objectives, endpoints & statistical rationale

  • Inclusion / exclusion criteria & risk–benefit assessment

  • Ethics Committee–ready & regulator-aligned formats suitable for Côte d’Ivoire and importing markets

  📊 Clinical Study Report (CSR) Writing

  • Full ICH E3–compliant Clinical Study Reports

  • Clinical data interpretation & scientific conclusions

  • Tables, Listings & Figures (TLFs)

  • Safety & efficacy evaluation

  • Investigator, site & multicenter data integration

  📁 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 reviews of CT documents

  • Gap assessment against ICH-GCP, WHO, US FDA, EMA & local MOH expectations

  • Scientific consistency, traceability & data integrity checks

  🛂 Post-Submission Query Handling

  • MOH / Ethics Committee / FDA query responses

  • Scientific rebuttals & clarifications

  • Deficiency letter responses

  • Regulatory follow-up support until approval or closure

  Industries We Serve in Côte d’Ivoire

  • Pharmaceutical Finished Dosage Forms

  • Nutraceuticals & Dietary Supplements

  • Herbal & Botanical Products

  • Functional Foods & Medical Nutrition

  • Generic & Branded Products

  • Export-oriented & multi-country clinical programs

  Global Regulatory Alignment

  Our Clinical Trial documentation is aligned with:

  • ICH-GCP (E6)

  • ICH E3 – Clinical Study Reports

  • WHO Guidelines

  • US FDA

  • EMA

  • GCC

  • African & LATAM MOH requirements

  • Country- and ethics committee–specific formats (Côte d’Ivoire & importing markets)

  Why Côte d’Ivoire–Based Clients Choose TrialTrust

  ✅ 330+ Clinical Trial Documents Delivered Globally
  ✅ Dedicated Clinical, Statistical & Regulatory Experts
  ✅ Strong Pharma & Nutraceutical specialization
  ✅ Authority-acceptable & inspection-ready documentation
  ✅ Proven post-submission query handling expertise
  ✅ Confidential, accurate & timeline-driven execution

  Our Experience Footprint

  • 330+ products supported worldwide

  • Clients across Asia, Middle East, Africa, Europe & LATAM

  • Experience in new products, line extensions & lifecycle management

  • Support for Côte d’Ivoire local registrations and global submissions

  Our Working Approach

  1. Requirement understanding & scope finalization

  2. Regulatory strategy & study design alignment

  3. Clinical document preparation / independent review

  4. Internal quality & scientific review

  5. Client review & finalization

  6. Post-submission authority & ethics committee query handling

  Confidentiality & Quality Commitment

  All projects are handled under strict confidentiality agreements, supported by robust quality systems, version control, and data integrity practices, ensuring regulatory confidence and global acceptance.