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

Brazil-Compliant | ANVISA & Global 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 Brazilian pharmaceutical, API, biotech, cosmetic, herbal, food, and chemical manufacturers supplying to domestic, LATAM, and international regulated markets.

Since 2008, BMRx has supported manufacturers across Latin America, North America, Europe, Africa, Asia, and the Middle East with regulatory-compliant, authority-acceptable BMR documentation, ensuring smooth approvals, inspection readiness, and reduced regulatory observations.

Who We Serve in Brazil

We work with Brazil-based companies involved in:

• Manufacturing for the Brazil domestic market
(ANVISA – Agência Nacional de Vigilância Sanitária)
• Export to US, EU, UK, LATAM, GCC, Africa & Asia
• API & intermediate manufacturing
• Finished dosage forms (OSD, injectables, sterile products, liquids, semi-solids)
• Contract manufacturing (CMOs & CDMOs)
• Technology transfer & scale-up projects
• ANVISA, US FDA, EU GMP & WHO inspections

Our BMR Services for Brazilian Manufacturers

We provide complete lifecycle support for Batch Manufacturing Records, including:

✅ BMR Preparation

• Preparation of Brazil-compliant and export-oriented BMRs aligned with:
o ANVISA GMP (RDC 301/2019 & related guidelines)
o US FDA (21 CFR Parts 210 & 211)
o EU GMP (EudraLex Volume 4)
o WHO GMP
o PIC/S GMP
• Product-specific, process-driven, non-generic BMRs
• Clear documentation of CPPs, IPCs, CQAs, yields, reconciliation, and deviations
• Operator-friendly, inspection-ready formats

✅ BMR Review & GMP Compliance Check

• Independent technical, GMP, and data-integrity review of existing BMRs
• Identification of:
o Missing ANVISA / PIC/S GMP elements
o ANVISA vs US FDA / EU GMP gaps
o Data integrity and traceability risks
o Inspection-critical weaknesses
• Alignment with current global regulatory expectations

✅ Regulatory Query & Inspection Support

• Support during ANVISA, US FDA, EU, and WHO inspections
• Handling of BMR-related authority queries:
o Pre-approval inspections
o Routine GMP audits
o For-cause inspections
• CAPA-linked BMR corrections and upgrades

✅ Gap Assessment & Remediation

• Detailed gap analysis of existing BMRs against:
o ANVISA / PIC/S GMP vs US FDA / EU GMP
o Export-market documentation expectations
• Practical, shop-floor-executable corrective actions
• Risk-based remediation for sterile, biotech, and high-risk processes

✅ Customized BMR Templates

• Regulator-accepted, ready-to-use BMR templates
• Custom-built based on:
o Dosage form & manufacturing technology
o Equipment trains & batch size
o Facility layout, utilities & automation
o Brazil domestic and global export requirements

Our Global Experience (Supporting Brazil from India)

• 3000+ BMRs prepared and reviewed
• Operational since 2008
• Extensive experience supporting Brazil → US / EU / WHO supply chains
• Strong exposure to:
o APIs & intermediates
o Oral solid dosage forms
o Injectables & sterile products
o Biopharma and high-compliance facilities
• Regular interaction with:
o ANVISA
o US FDA
o EU Competent Authorities
o WHO / PIC/S regulators

Regulatory Standards Followed

All BMR documentation is prepared in line with:

• ANVISA GMP (RDC 301/2019)
• PIC/S GMP Requirements
• EU GMP (EudraLex Volume 4)
• WHO GMP Guidelines
• US FDA cGMP (21 CFR Parts 210 & 211)
• ICH Q7 / Q8 / Q9 / Q10
• Import-country MOH and authority expectations

Industries We Support in Brazil

• Pharmaceuticals & APIs
• Finished Dosage Forms
• Injectables & Sterile Products
• Biopharma & Advanced Therapies (documentation support)
• Cosmetics & Personal Care
• Herbal & Natural Products
• Food & Nutraceutical Ingredients
• Chemicals & Industrial Products

Why Brazilian Manufacturers Choose BMRx

• 🇧🇷 Strong alignment with ANVISA & PIC/S GMP expectations
• 🌍 Export-oriented BMRs accepted globally
• 📋 Inspection-ready, auditable documentation
• 🔍 Reduced ANVISA / US FDA / EU GMP observations
• 🧠 Technical + GMP + regulatory expertise
• 🛠️ Non-generic, process-specific BMRs
• 🔒 Confidential, professional, and deadline-driven
• 👷 Operator-friendly formats for shop-floor execution

How We Start the Project

To initiate BMR preparation or review, we typically require:

• Product and formulation details
• Manufacturing process & flow diagram
• Equipment list and batch size
• Target export markets and regulatory strategy
• 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 Brazilian manufacturers for LATAM & global regulatory success