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

BPOM-Compliant | CPOB & WHO GMP Aligned | 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 in Indonesia supplying to domestic and international regulated markets.

Since 2008, BMRx has supported manufacturers across Asia with regulatory-compliant, authority-acceptable BMR documentation, ensuring compliance with BPOM Indonesia, CPOB, WHO GMP, and global inspection readiness.

Who We Serve in Indonesia

We work with Indonesia-based organizations involved in:

• Manufacturing for the Indonesian domestic market (BPOM)
• Export to ASEAN, US, EU, UK, GCC, Africa & LATAM
• Contract manufacturing (CMOs / CDMOs)
• Technology transfer, scale-up & localization projects
• New manufacturing site approvals & BPOM licensing
• BPOM, WHO & international regulatory inspections

Our BMR Services for Indonesia Manufacturers

✅ BMR Preparation

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

• BPOM Indonesia – CPOB 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 & CPPs
• Inspection-ready documentation acceptable to BPOM & global authorities

✅ BMR Review & CPOB / GMP Compliance Check

Independent technical and GMP review of existing BMRs to identify:

• Missing BPOM / CPOB elements
• Data integrity & documentation gaps
• Inspection-critical weaknesses
• Non-alignment with export market expectations

Deliverables include clear, implementable remediation recommendations.

✅ Regulatory Query & Inspection Support

Support during:

• BPOM post-submission queries
• BPOM GMP inspections & re-inspections
• WHO audits & customer 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:

• BPOM CPOB requirements
• WHO GMP expectations
• PIC/S & export market MOH requirements

With practical, floor-ready corrective actions suitable for Indonesian manufacturing operations.

✅ Customized BMR Templates

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

• Dosage form
• Equipment & batch size
• Manufacturing process
• Facility layout & utilities
• Target domestic & export markets

Our Global Experience (Supporting Indonesia from India)

• 3000+ BMRs prepared & reviewed
• Operational since 2008
• Experience across:
– Indonesia
– ASEAN
– India
– Middle East
– Africa
– Europe
– LATAM

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

Regulatory Interaction Experience With:
• BPOM Indonesia
• WHO
• US FDA
• EU Authorities
• PIC/S Regulators

Regulatory Standards Followed

All BMR documentation is prepared in accordance with:

• BPOM Indonesia – CPOB
• 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 expectations for exports

Industries We Support in Indonesia

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

Why Indonesia Manufacturers Choose BMRx

• 🇮🇩 Strong understanding of BPOM & CPOB requirements
• 🌍 Export-oriented BMRs accepted globally
• 📋 Inspection-ready & auditable documentation
• 🔍 Reduced inspection observations
• 🧠 Integrated technical, GMP & regulatory expertise
• 🛠️ Non-generic, process-specific BMRs
• 🔒 Confidential, professional & deadline-driven delivery
• 👷 Operator-friendly formats for shop-floor execution

How We Initiate a BMR Project

To initiate BMR preparation or review, we typically require:

• Product & formulation details
• Manufacturing process & flow diagram
• Equipment list & batch size
• Target markets & regulatory pathway
• 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 Indonesian manufacturers for global regulatory success.