Regulatory And Research Services for Tanzania
🇹🇿 Regulatory and Research Services for Tanzania – Dossier-DMF Services @ Zoesoe Exports Pvt Ltd
We, Zoesoe Exports Pvt Ltd, specialize in providing end-to-end regulatory and research services for pharmaceutical, nutraceutical, herbal, and cosmetic companies aiming to enter the Tanzania market.
Our services ensure full compliance with the Tanzania Medicines and Medical Devices Authority (TMDA), as well as WHO and ICH guidelines.
📘 Regulatory Services for Tanzania
Regulatory & Product Registration Support – Tanzania
We assist pharmaceutical, nutraceutical, and cosmetic companies in dossier preparation, submission, and product registration with TMDA, ensuring smooth market access and full regulatory compliance.
📘 Product Registration Services
• Preparation and submission of registration dossiers for prescription (Rx) and OTC products.
• Registration support for Herbal, Traditional, Nutraceutical, Veterinary, and Cosmetic products.
• Guidance on labeling, packaging, and product information leaflets according to TMDA regulations.
📗 Drug Master File (DMF) Services
• Compilation of CTD/ACTD-compliant DMFs for APIs intended for registration in Tanzania.
• Support in preparing quality, safety, and stability documentation in line with TMDA and ICH standards.
⚗️ Bioequivalence (BE) Study Support
• Design and coordination of BE studies in TMDA-approved CROs.
• Preparation of BE study protocols and reports according to WHO and TMDA requirements.
🔬 Analytical Method Validation (AMV) Services
• Validation of analytical methods in compliance with ICH Q2(R2).
• Preparation of AMV documentation for regulatory submission and routine QC.
🧾 Regulatory Consultancy & Compliance
• Strategic regulatory guidance for entry into the Tanzania market.
• Assistance with import/export licensing, TMDA inspections, renewals, and post-approval compliance.
• Continuous updates on TMDA regulatory changes to ensure product compliance.
🧪 Research & Development (R&D) Services – Tanzania
Our R&D services support formulation development, analytical validation, and quality assurance activities in compliance with TMDA and international standards.
💊 Formulation Development
• Development and optimization of tablets, capsules, syrups, powders, and injectables.
• Stability studies designed for Tanzania’s climatic conditions.
🧫 Analytical R&D Services
• Assay, dissolution, impurity profiling, and stability testing.
• Analytical method development and transfer to partner laboratories per TMDA requirements.
📑 Product Development Reports (PDRs)
• Preparation of comprehensive PDRs for submission to TMDA.
• Inclusion of formulation, manufacturing, QC, and stability data.
🧍⚕️ Clinical Trial & Toxicology Support
• Preparation of clinical trial protocols, investigator brochures, and final reports.
• Toxicology studies according to OECD and WHO guidelines for TMDA submission.
🌏 Why Choose Us for the Tanzania Market
• Experienced Regulatory Experts – Skilled in TMDA, WHO, and ICH regulatory frameworks.
• End-to-End Support – From dossier preparation to post-approval compliance.
• Regional Expertise – Proven success across East Africa.
• Efficient Documentation – Streamlined processes for faster regulatory approvals.
• Custom Strategies – Tailored per product type, regulatory pathway, and market requirements.
📘 Regulatory & Dossier Documentation
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⚗️ Bioequivalence & Analytical Studies
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🧪 Technology Transfer & Safety
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