Regulatory And Research Services for Democratic-Republic-of-the-Congo-(Zaire)
🇨🇩 Regulatory and Research Services for Democratic Republic of the Congo – 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 DR Congo market.
Our services ensure full compliance with the Direction de la Pharmacie et du Médicament (DPM DRC), as well as WHO and ICH guidelines.
📘 Regulatory Services for DR Congo
Regulatory & Product Registration Support – DR Congo
We assist pharmaceutical, nutraceutical, and cosmetic companies in dossier preparation, submission, and product registration with DPM DRC, 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 DPM DRC regulations.
📗 Drug Master File (DMF) Services
• Compilation of CTD/ACTD-compliant DMFs for APIs intended for registration in DR Congo.
• Support in preparing quality, safety, and stability documentation in line with DPM DRC and ICH standards.
⚗️ Bioequivalence (BE) Study Support
• Design and coordination of BE studies in DPM-approved CROs.
• Preparation of BE study protocols and reports according to WHO and DPM DRC 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 DR Congo market.
• Assistance with import/export licensing, DPM DRC inspections, renewals, and post-approval compliance.
• Continuous updates on DPM DRC regulatory changes to ensure product compliance.
🧪 Research & Development (R&D) Services – DR Congo
Our R&D services support formulation development, analytical validation, and quality assurance activities in compliance with DPM DRC and international standards.
💊 Formulation Development
• Development and optimization of tablets, capsules, syrups, powders, and injectables.
• Stability studies designed for DR Congo’s climatic conditions.
🧫 Analytical R&D Services
• Assay, dissolution, impurity profiling, and stability testing.
• Analytical method development and transfer to partner laboratories per DPM DRC requirements.
📑 Product Development Reports (PDRs)
• Preparation of comprehensive PDRs for submission to DPM DRC.
• 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 DPM DRC submission.
🌏 Why Choose Us for the DR Congo Market
• Experienced Regulatory Experts – Skilled in DPM DRC, WHO, and ICH regulatory frameworks.
• End-to-End Support – From dossier preparation to post-approval compliance.
• Regional Expertise – Proven success across Central 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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🌐 Top Pharma & Regulatory Hashtags – DR Congo
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