BMRx – Global Batch Manufacturing Record (BMR) Services for Fiji

Fiji MOH–Aligned | WHO GMP Compliant | Inspection-Ready

BMRx is a specialized scientific arm of Zoesoe Exports Pvt Ltd, providing end-to-end Batch Manufacturing Record (BMR) Preparation & Review Services for pharmaceutical and regulated-industry manufacturers and suppliers serving the Fiji market and wider Pacific Island / international supply chains.

Since 2008, BMRx has supported manufacturers across Asia-Pacific, Oceania, and global markets with regulatory-compliant, authority-acceptable BMR documentation, ensuring alignment with the Fiji Ministry of Health & Medical Services (MHMS), Pharmaceutical & Biomedical Services Centre (PBSC), WHO GMP, and global inspection readiness.

Who We Serve in Fiji

We work with Fiji-based and Fiji-focused organizations involved in:

• Manufacturing for the Fiji domestic market (MOH / PBSC)
• Importation, repacking & secondary manufacturing
• Supply to Pacific Island countries & donor-funded programs
• Contract manufacturing (CMOs / CDMOs)
• Technology transfer & scale-up projects
• MOH inspections, WHO audits & donor assessments

Our BMR Services for Fiji Market Products

✅ BMR Preparation

We prepare product-specific, process-driven BMRs aligned with:

• Fiji MOH / PBSC GMP requirements
• WHO GMP Guidelines
• US FDA cGMP (21 CFR Parts 210 & 211)
• EU GMP Guidelines
• PIC/S GMP Requirements

Key Features
• Non-generic, facility-specific BMRs
• Operator-friendly & shop-floor executable formats
• Clearly defined IPCs, CPPs & yields
• Inspection-ready documentation acceptable to Fiji MOH, WHO & donor agencies

✅ BMR Review & GMP Compliance Check

Independent technical and GMP review of existing BMRs to identify:

• Missing Fiji MOH / WHO GMP elements
• Documentation & data-integrity gaps
• Inspection-critical weaknesses
• Non-alignment with donor & export-market expectations

Deliverables include clear, implementable remediation recommendations.

✅ Regulatory Query & Inspection Support

Support during:

• Fiji MOH / PBSC post-submission queries
• MOH GMP inspections & follow-ups
• WHO audits & donor-funded program reviews
• Export-market regulatory assessments

Including:
• Authority query responses
• Inspection observation remediation
• CAPA-linked BMR updates

✅ Gap Assessment & Remediation

Comprehensive gap analysis of existing BMRs against:

• Fiji MOH GMP requirements
• WHO GMP expectations
• PIC/S & export-market MOH requirements

With practical, floor-ready corrective actions suitable for Fiji-linked manufacturing and supply environments.

✅ Customized BMR Templates

Provision of ready-to-use, regulator-accepted BMR templates, customized based on:

• Dosage form
• Equipment & batch size
• Manufacturing / packaging process
• Facility layout & utilities
• Target Fiji, Pacific Islands & export markets

Our Global Experience (Supporting Fiji from India)

• 3000+ BMRs prepared & reviewed
• Operational since 2008
• Experience across:
– Fiji & Pacific Islands
– Asia-Pacific
– Africa
– Middle East
– Europe
– LATAM

Product Categories Supported
• Finished dosage forms
• APIs & intermediates
• Sterile & non-sterile products
• Herbal & traditional medicines
• Nutraceuticals & food ingredients
• Cosmetics & personal care

Regulatory Interaction Experience With
• Fiji Ministry of Health & Medical Services (MHMS)
• WHO
• US FDA
• EU Authorities
• PIC/S Regulators

Regulatory Standards Followed

All BMR documentation is prepared in accordance with:

• Fiji MOH / PBSC GMP Guidelines
• WHO GMP
• US FDA cGMP (21 CFR 210 & 211)
• EU GMP
• PIC/S GMP Requirements
• ICH Q7 / Q8 / Q9 / Q10 (where applicable)
• Country-specific MOH & donor-procurement expectations

Industries We Support in Fiji

• Pharmaceutical Finished Dosage Forms
• APIs & Bulk Drugs
• Sterile & Injectable Products
• Herbal & Traditional Medicines
• Nutraceuticals & Food Ingredients
• Cosmetics & Personal Care
• Disinfectants & Essential Medical Supplies

Why Fiji Market Companies Choose BMRx

• 🇫🇯 Strong understanding of Fiji MOH & WHO GMP expectations
• 🌍 Export- & donor-oriented BMRs accepted internationally
• 📋 Inspection-ready & auditable documentation
• 🔍 Reduced regulatory & donor audit observations
• 🧠 Integrated technical, GMP & regulatory expertise
• 🛠️ Non-generic, process-specific BMRs
• 🔒 Confidential, professional & deadline-driven delivery
• 👷 Operator-friendly formats for reliable execution

How We Initiate a BMR Project

To initiate BMR preparation or review, we typically require:

• Product & formulation details
• Manufacturing / packaging process & flow diagram
• Equipment list & batch size
• Target markets & procurement channels
• Existing BMRs (if available)

Based on this, we provide:

• Customized technical scope
• Clear timelines
• Transparent commercial proposal

BMRx

Batch Manufacturing Records. Built for Compliance. Ready for Inspection.
Supporting Fiji manufacturers for Pacific Island, donor-funded & global regulatory success