Drug Master File (DMF) Preparation, Review & Regulatory Support Services – Nashik

CDSCO West Zone & Maharashtra FDA–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 for pharmaceutical manufacturers, formulation units, API traders, exporters, and contract manufacturing companies based in Nashik and surrounding MIDC industrial areas.

Our DMF services are fully aligned with:

• Central Drugs Standard Control Organization (CDSCO – West Zone, Mumbai)

• Maharashtra State Food & Drug Administration (Maharashtra FDA)

And comply with:

• Drugs & Cosmetics Act & Rules, India

• Schedule M (GMP)

• ICH Guidelines

• CTD / eCTD-based dossier formats

Supporting regulatory filings for:

• API registration
• Finished formulation approvals
• Import registration dossiers
• Export-oriented regulatory submissions
• Contract manufacturing & technology transfer filings

We specialize in the preparation and maintenance of both:

1. Open Part (Applicant’s Part)

2. Closed Part (Restricted / Confidential Part)

Ensuring full regulatory compliance, strict confidentiality, and smooth approvals for Nashik-based manufacturers and exporters.

Our Core DMF Services – Nashik

🧪 DMF Preparation – Open & Closed Parts (India & Nashik–Compliant)

We prepare complete, structured, and CDSCO-aligned DMF dossiers in CTD format accepted for:

• India
• USA (USDMF)
• EU (ASMF)
• GCC & MENA
• ASEAN
• Africa & LATAM

Applicant’s Part (Open Part) – Nashik

Prepared for submission to CDSCO / Maharashtra FDA / Applicants, including:

• Quality Overall Summary (QOS) aligned with ICH Q2–Q6
• Non-confidential manufacturing & quality information
• Cross-reference-ready documentation for:
– Form 44 / New Drug Applications
– Import Registration (Form 10 / Form 41)
– Manufacturing License (Form 25 / Form 28)
– Export Registration Dossiers
• CTD-structured documentation suitable for domestic and international regulatory filings

Restricted Part (Closed / Confidential Part)

Secure preparation and handling of proprietary technical data, including:

• Detailed manufacturing process & flow diagrams
• Critical process parameters & in-process controls
• Raw material, intermediates & finished product specifications
• Analytical methods & validation (ICH Q2)
• Control strategy & Pharmaceutical Quality System (PQS)
• Stability data as per Indian climatic conditions (Zone IVb)

✅ Confidential data is accessed only by regulatory authorities and never disclosed to applicants.

DMF Types Covered – Nashik

• Type II – Active Pharmaceutical Ingredients (API)
• Type III – Packaging Materials
• Type IV – Excipients
• Type V – Reference / Miscellaneous Information

🧪 DMF Review & Gap Assessment – Nashik

Already have a DMF prepared in Nashik?

We conduct India-specific and export-ready DMF reviews based on:

• CDSCO West Zone & Maharashtra FDA inspection expectations
• Schedule M & WHO-GMP compliance gaps
• CTD structure & documentation deficiencies
• Manufacturing, validation & stability inconsistencies
• Likely regulatory deficiency triggers

✔️ You receive a detailed, actionable gap assessment report before submission or inspection.

🧪 CDSCO & Maharashtra FDA Submission Support – Nashik

We provide hands-on regulatory support, including:

• CDSCO submissions & technical justifications
• Maharashtra FDA manufacturing license documentation
• API registration & DMF linkage support
• Import-export regulatory documentation
• Global submission DMF alignment (USA, EU, GCC, ASEAN, Africa, LATAM)

We ensure:

• Correct CTD / eCTD formatting
• Accurate cross-referencing
• Full consistency across DMF, applications & manufacturing records

🧪 DMF Lifecycle Management & Maintenance – Nashik

We manage your DMF through its complete regulatory lifecycle:

• Initial DMF compilation
• Annual updates & renewals
• Manufacturing site changes
• Process optimization & scale-up documentation
• Stability updates (real-time & accelerated)
• API & specification changes
• CDSCO-driven amendments & responses

🧪 Post-Submission Deficiency & Query Handling – Nashik

End-to-end regulatory query & deficiency response management, including:

• CDSCO deficiency letters & Maharashtra FDA audit observations
• Scientific justification drafting
• Revised Open & Closed Part submissions
• Alignment with applicant & exporter responses
• Coordination between manufacturer, consultants & regulators

🎯 Goal: Faster approvals, minimal queries, and regulator-ready dossiers.

🧪 Why Choose DMF Direct in Nashik?

🧪 Strong experience with Nashik MIDC pharma & formulation manufacturing clusters
🧪 Deep working exposure with Maharashtra FDA & CDSCO West Zone
🧪 Expertise in Schedule M, WHO-GMP & ICH-aligned DMF
🧪 Secure confidential data handling
🧪 Proven CDSCO deficiency response success
🧪 Backed by Zoesoe Exports Pvt Ltd’s global regulatory strength

Industries We Support – Nashik

• API manufacturers & traders
• Finished formulation (FDF) manufacturers
• Nutraceutical & herbal product manufacturers
• Biotech & specialty pharma companies
• Excipient & packaging suppliers
• Exporters & importers
• Contract Manufacturing Organizations (CMOs)

Regulatory Standards Followed – Nashik

• Drugs & Cosmetics Act & Rules (India)
• CDSCO & Maharashtra FDA Guidelines
• Schedule M (GMP)
• ICH Q & M Series
• CTD / eCTD
• WHO-GMP & Global Regulatory Standards

Your Trusted DMF Partner in Nashik

Whether you are a formulation unit in Ambad MIDC, an API trader in Satpur, a nutraceutical manufacturer near Sinnar, or an exporter based in Nashik Road, DMF Direct delivers high-quality, compliant, and approval-focused DMF solutions from Nashik to global markets.

✅ Regulatory-aligned
✅ Confidential
✅ Efficient
✅ Approval-driven

If you want, I can also prepare:

✅ SEO landing page for “DMF Services in Nashik”
✅ Maharashtra pharma-focused brochure version
✅ Export-focused DMF services page for Nashik manufacturers