BMRx – Global Batch Manufacturing Record (BMR) Services for Côte d’Ivoire

• MOH Côte d’Ivoire–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 supplying to Côte d’Ivoire and the wider West African region.

  Since 2008, BMRx has supported manufacturers across Africa and global export markets with regulatory-compliant, authority-acceptable BMR documentation, ensuring alignment with the Ministry of Health & Public Hygiene (MSHP) / National Medicines Regulatory Authority of Côte d’Ivoire, WHO GMP, and global inspection readiness.

  Who We Serve in Côte d’Ivoire

  We work with Côte d’Ivoire–focused organizations involved in:

  • Manufacturing for the Côte d’Ivoire domestic market (MOH / NMRA)
  • Importation, local packaging & secondary manufacturing
  • Export to ECOWAS & WAEMU (UEMOA) markets
  • Contract manufacturing (CMOs / CDMOs)
  • Technology transfer & scale-up projects
  • MOH inspections, WHO audits & donor / customer assessments

  Our BMR Services for Côte d’Ivoire Market Products

  ✅ BMR Preparation

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

  • Côte d’Ivoire MOH 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
  • Clear in-process controls, yields & critical parameters
  • Inspection-ready documentation acceptable to MOH, WHO & regional authorities

  ✅ BMR Review & GMP Compliance Check

  Independent technical and GMP review of existing BMRs to identify:

  • Missing Côte d’Ivoire MOH / WHO GMP elements
  • Documentation & data-integrity gaps
  • Inspection-critical weaknesses
  • Non-alignment with ECOWAS & donor-procurement expectations

  Deliverables include clear, implementable remediation recommendations.

  ✅ Regulatory Query & Inspection Support

  Support during:

  • Côte d’Ivoire MOH post-submission queries
  • MOH GMP inspections & follow-ups
  • WHO audits & donor / procurement inspections
  • Export-market regulatory reviews

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

  ✅ Gap Assessment & Remediation

  Comprehensive gap analysis of existing BMRs against:

  • Côte d’Ivoire MOH GMP requirements
  • WHO GMP expectations
  • PIC/S & export-market MOH requirements

  With practical, floor-ready corrective actions suitable for Côte d’Ivoire-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 domestic, ECOWAS & export markets

  Our Global Experience (Supporting Côte d’Ivoire from India)

  • 3000+ BMRs prepared & reviewed
  • Operational since 2008
  • Experience across:
  – Côte d’Ivoire
  – West & Central Africa (ECOWAS / UEMOA)
  – Middle East
  – Asia
  – Europe
  – LATAM

  Product Categories Supported:
  • Finished dosage forms
  • APIs & intermediates
  • Herbal & traditional medicines
  • Nutraceuticals & food ingredients
  • Cosmetics & personal care
  • Chemicals & disinfectants

  Regulatory Interaction Experience With:
  • MOH Côte d’Ivoire / National Medicines Authorities
  • WHO
  • US FDA
  • EU Authorities
  • PIC/S Regulators

  Regulatory Standards Followed

  All BMR documentation is prepared in accordance with:

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

  Industries We Support in Côte d’Ivoire

  • Pharmaceutical Finished Dosage Forms
  • APIs & Bulk Drugs
  • Herbal & Traditional Medicines
  • Nutraceuticals & Food Ingredients
  • Cosmetics & Personal Care
  • Industrial & Specialty Chemicals

  Why Côte d’Ivoire Market Companies Choose BMRx

  • 🇨🇮 Strong understanding of Côte d’Ivoire MOH & WHO GMP expectations
  • 🌍 Export- & donor-oriented BMRs accepted across West Africa
  • 📋 Inspection-ready & auditable documentation
  • 🔍 Reduced regulatory & procurement 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 Côte d’Ivoire market products for regional and global regulatory success.