Drug Master File (DMF) Preparation, Review & Regulatory Support Services – Mozambique
ANARME-Compliant DMF Documentation & Regulatory Support
By DMF Direct – A Scientific Arm of Zoesoe Exports Pvt Ltd
DMF Direct provides end-to-end Drug Master File (DMF) preparation, review, submission, and lifecycle management services specifically tailored for Mozambique’s regulatory framework.
Our DMF services are designed to meet the expectations of the Autoridade Nacional Reguladora de Medicamentos (ANARME), Mozambique and align with:
• Law on Medicines & Pharmaceutical Products – Mozambique
• ANARME Guidelines for Registration of Medicinal Products
• WHO GMP Standards
• ICH Guidelines
• CTD-based documentation formats
• SADC & ZAZIBONA Harmonized Regulatory Requirements
Used for:
• API registration
• Finished formulation product registration
• Import authorization dossiers
• Export-oriented regulatory filings
We specialize in the preparation and maintenance of both:
Open Part (Applicant’s Part)
Closed Part (Restricted / Confidential Part)
Ensuring regulatory compliance, confidentiality, and smooth approval processing in Mozambique.
Our Core DMF Services – Mozambique
🧪 DMF Preparation – Open & Closed Parts (Mozambique-Compliant)
We prepare complete, structured, and ANARME-aligned DMF dossiers following CTD format accepted for Mozambican submissions.
Applicant’s Part (Open Part)
Prepared for submission to ANARME Mozambique / Local Marketing Authorization Holders / Importers, including:
• Quality Overall Summary (QOS) aligned with ICH Q2–Q6
• Non-confidential manufacturing and quality information
• Cross-reference-ready content for:
– Product registration
– Import authorization
– Marketing authorization
• CTD-structured documentation suitable for Mozambique and SADC/ZAZIBONA markets
Restricted Part (Closed / Confidential Part)
Secure preparation and handling of proprietary technical information, including:
• Detailed manufacturing process and process flow diagrams
• Critical process parameters and in-process controls
• Raw material, intermediates, and finished product specifications
• Analytical methods and method validation (ICH Q2)
• Control strategy and pharmaceutical quality systems
• Stability data as per WHO Climatic Zone IVb (hot & humid – applicable to Mozambique)
✅ Confidential information is shared only with ANARME regulators and never with applicants.
DMF Types Covered – Mozambique
We support DMF documentation for:
• Type II – Active Pharmaceutical Ingredient (API), Intermediates
• Type III – Packaging Materials
• Type IV – Excipients
• Type V – Reference / Miscellaneous Information
🧪 DMF Review & Gap Assessment – Mozambique
Already have a DMF for Mozambique?
We conduct Mozambique-specific DMF review and risk assessment based on:
• ANARME regulatory expectations and inspection observations
• WHO GMP compliance gaps
• CTD structure and content deficiencies
• Manufacturing, validation, and stability inconsistencies
• Likely ANARME technical deficiency triggers
✔️ You receive a clear, actionable gap assessment report prior to submission or inspection.
🧪 ANARME Submission & Mozambique Regulatory Support
We provide hands-on support for DMF usage and filing in Mozambique, including:
• ANARME submissions and technical clarifications
• API registration support
• Import authorization dossier preparation
• Finished product registration documentation
• Export-linked DMF alignment
Our team ensures:
• Correct CTD formatting
• Accurate technical cross-referencing
• Full consistency across DMF, product dossiers, and manufacturing documents
🧪 DMF Lifecycle Management & Maintenance – Mozambique
We manage your DMF throughout its complete regulatory lifecycle, including:
• Initial DMF compilation
• Annual updates and regulatory renewals
• Manufacturing site changes
• Process optimization or scale-up documentation
• Stability updates (accelerated & long-term)
• Specification and analytical method revisions
• ANARME-driven amendments and updates
🧪 Post-Submission Deficiency & Query Handling – ANARME Mozambique
Complete post-submission regulatory support, including:
• ANARME deficiency letters and technical queries
• Scientific justification and response drafting
• Revised Open & Closed Part submissions
• Alignment with applicant responses
• Coordination between manufacturer, importer, and ANARME authority
🎯 Goal: Faster approvals, fewer queries, and regulator-ready DMF documentation.
🧪 Why Choose DMF Direct for Mozambique?
🧪 In-depth knowledge of ANARME & SADC/ZAZIBONA regulatory pathways
🧪 Strong expertise in WHO GMP and ICH-aligned DMF documentation
🧪 Secure handling of confidential manufacturing data
🧪 Proven experience in regulatory deficiency responses
🧪 Seamless coordination with Mozambican importers & MA holders
🧪 Supported by Zoesoe Exports Pvt Ltd’s regulatory strength
Industries We Support – Mozambique
• API manufacturers
• Finished formulation manufacturers (FDF)
• Excipient manufacturers
• Packaging material suppliers
• Importers and distributors
• Contract manufacturing organizations (CMOs)
Regulatory Standards Followed – Mozambique
• National Medicines Law – Mozambique
• ANARME Guidelines
• WHO GMP
• ICH Q-Series & M-Series Guidelines
• CTD / eCTD-ready documentation
• SADC / ZAZIBONA Harmonized Technical Guidelines (where applicable)
Your Trusted Partner for DMF Excellence in Mozambique
Whether you are preparing a new DMF, updating an existing dossier, supporting an ANARME submission, or responding to regulatory queries, DMF Direct delivers high-quality, compliant, and approval-focused DMF solutions for the Mozambican pharmaceutical market.
✅ Regulatory-aligned
✅ Confidential
✅ Efficient
✅ Approval-driven