DossierTrans – Burkina Faso

Burkina Faso Dossier & Technical Document Translation Services

Accurate. Regulatory-Compliant. Authority-Ready.

DossierTrans, a scientific arm of Zoesoe Exports Pvt Ltd, provides end-to-end translation, technical review, and regulatory query support for Burkina Faso–specific dossiers and technical documents, aligned with national regulatory authorities and statutory requirements.

We support Burkinabè manufacturers, importers, exporters, marketing authorization holders, NGOs, and regulatory teams with precise, technically accurate, and authority-acceptable translations, ensuring smooth submissions, inspections, and regulatory approvals in Burkina Faso.

Who We Are

DossierTrans is a specialized regulatory translation service provider for the Burkina Faso market, focused exclusively on scientific, pharmaceutical, and technical documentation.

All translations are performed and reviewed by subject-matter experts, regulatory professionals, and technical reviewers—not general translators.

We ensure every translated dossier preserves:

• Scientific accuracy
• Regulatory intent
• Terminology consistency
• Compliance with Burkina Faso–specific MoH / DGPML expectations

Burkina Faso Regulatory Alignment

Our services are aligned with the requirements of:

Ministry of Health (Ministère de la Santé), Burkina Faso
General Directorate of Pharmacy, Medicines and Laboratories (DGPML)
Burkina Faso Medicines Registration Regulations
West African Health Organization (WAHO / OOAS) guidelines
ECOWAS pharmaceutical harmonization initiatives
Burkina Faso Customs Administration
• Other applicable import & export regulatory authorities in Burkina Faso

Our Core Services – Burkina Faso

📘 Dossier & Technical Document Translation

• Burkina Faso–specific CTD / non-CTD dossier formats
Module 1–5 translations for DGPML submissions
• Prescribing information, labels, package inserts, leaflets & artwork text (French-compliant)
• Stability studies, analytical validation & study reports
• SOPs, specifications, COAs, SDS & technical documentation
• Product registration, import authorization & export documentation

🔍 Review of Translated Dossiers

• Scientific and technical review of translated documents
• Cross-verification with source-language dossiers
• Identification of terminology errors, inconsistencies & regulatory gaps
• Alignment with DGPML requirements, WAHO guidance, and accepted pharmacopoeias (USP, BP, EP)

🛡️ Post-Submission Regulatory Query Handling – Burkina Faso

DGPML / Ministry of Health queries related to translated content
• Scientific clarification and regulatory re-wording support
• Revised translations based on authority observations
• Coordination with applicants, local agents, NGOs, distributors, and consultants

Languages We Support (Burkina Faso-Focused)

🌍 International Languages

• English
• French
• German
• Spanish
• Italian
• Portuguese
• Russian
• Arabic
• Chinese (Simplified & Traditional)
• Japanese
• Korean

🇧🇫 Local & Regional Language Support

French (official regulatory language)
• English (for import/export dossiers)

English ↔ French | Foreign Language ↔ English / French

All translations are reviewed by regulatory experts experienced with DGPML and ECOWAS-aligned requirements.

Industries We Serve – Burkina Faso

• Pharmaceuticals & APIs
• Medical Devices
• Vaccines & Biologicals
• Cosmetics & Personal Care
• Food & Nutraceutical Ingredients
• Herbal & Traditional Medicines
• Essential Oils & Fragrances
• Agrochemicals
• Industrial & Specialty Chemicals

Why Choose DossierTrans for Burkina Faso?

✅ Burkina Faso–regulatory-focused translation (not generic translation)
✅ Proven expertise in DGPML & ECOWAS-aligned documentation
✅ Native French-language scientific & regulatory reviewers
✅ Terminology consistency across Burkina Faso submissions
✅ Authority-ready, inspection-friendly documentation
✅ End-to-end support including post-submission regulatory queries
✅ Strict confidentiality & data security

Global & Burkina Faso Regulatory Expertise

Our Burkina Faso services support:

• DGPML product registration & import authorization dossiers
• Manufacturing & marketing authorization documentation
• Export-support translations for ECOWAS, Francophone Africa & ROW markets
• Post-approval variations, renewals & lifecycle management

Our Commitment

At DossierTrans, we understand that a single mistranslated sentence can delay or reject a DGPML approval in Burkina Faso.

That’s why we deliver precision-driven, regulator-acceptable translations, fully aligned with Burkinabè compliance expectations—every time.

DossierTrans – Translating Science into Regulatory Approval in Burkina Faso

If you’d like next, I can:
✔ Prepare SEO-optimized Burkina Faso landing page content
✔ Create French–English bilingual brochures
✔ Develop DGPML-only pharma or ECOWAS-harmonized versions
✔ Convert this for Mali, Niger, Senegal, Côte d’Ivoire, GCC, or LATAM