TrialTrust Global Clinical Trial Document Writing & Review Services in Burundi

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 delivered 330+ clinical trial documentation projects for sponsors, CROs, and manufacturers across Burundi, East Africa, Asia, Europe, 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 robust scientific data, strong clinical justification, and regulatory-aligned documentation suitable for Burundi Ministry of Public Health submissions and East African regulatory authorities.

Our Services for Clients in Burundi

🧪 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 & Ministry of Public Health-ready formats

📊 Clinical Study Report (CSR) Writing

  • Full Clinical Study Reports compliant with ICH E3

  • 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, WHO, EMA, USFDA & Burundi Ministry of Public Health requirements

  • Scientific consistency & data integrity checks

🛂 Post-Submission Query Handling

  • Responses to Burundi Ministry of Public Health & Ethics Committees

  • Scientific rebuttals & clarifications

  • Deficiency letter responses

  • Regulatory follow-up support until closure

Industries We Serve in Burundi

  • Pharmaceutical Finished Dosage Forms

  • Generic & Branded Medicines

  • Nutraceuticals & Dietary Supplements

  • Herbal & Botanical Products

  • Functional Foods & Medical Nutrition

  • Export-oriented clinical programs

Burundi & East African Regulatory Alignment

Our Clinical Trial documentation is prepared in alignment with:

  • ICH-GCP (E6)

  • ICH E3 – Clinical Study Reports

  • WHO Guidelines

  • Burundi Ministry of Public Health regulations

  • USFDA & EMA reference standards

  • Country-specific Ethics Committee formats

Why Companies in Burundi Choose TrialTrust

330+ Clinical Trial Documents Delivered Globally
Experienced East African & Global Clinical & Regulatory Experts
Strong Pharma & Nutraceutical Specialization
Authority-Acceptable & Inspection-Ready Documentation
Comprehensive Post-Submission Support
Confidential, Accurate & Timeline-Driven Execution

Our Experience Footprint

  • 330+ products supported worldwide

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

  • Expertise in emerging and regulated African markets

  • Support for local Burundi registrations and regional East African submissions

Our Working Approach

  1. Requirement Understanding & Scope Finalization

  2. Regulatory Strategy & Study Design Alignment

  3. Clinical Document Preparation / Review

  4. Internal Scientific & Quality Review

  5. Client Review & Finalization

  6. Post-Submission Authority Query Handling

Confidentiality & Quality Commitment

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

Contact TrialTrust in Burundi

Looking for reliable, authority-ready 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 requirements in Burundi.