TajikistanSSSHSPP-Aligned BA/BE & Comparative Dissolution Profiling Services — By BioEqui
Tajikistan MOH–Aligned | WHO GMP Compliant | Inspection-Ready
BMRx is a specialized scientific arm of Zoesoe Exports Pvt Ltd, delivering end-to-end Batch Manufacturing Record (BMR) Preparation & Review Services for pharmaceutical and regulated-industry manufacturers and MAHs supplying to the Tajikistan market and neighboring regional markets.
Since 2008, BMRx has supported manufacturers across Central Asia, CIS, Eurasia, and global markets with regulatory-compliant, authority-acceptable BMR documentation, ensuring alignment with the Ministry of Health and Social Protection of the Population of the Republic of Tajikistan (MOHSPP), WHO GMP, and global inspection readiness.
Who We Serve in Tajikistan
We work with Tajikistan-based and Tajikistan-focused organizations involved in:
• Manufacturing for the Tajikistan domestic market (MOHSPP)
• Importation, local packaging & secondary manufacturing
• Export to Central Asia, CIS & Eurasian markets
• Contract manufacturing (CMOs / CDMOs)
• Technology transfer & scale-up projects
• MOH inspections, WHO audits & customer inspections
Our BMR Services for Tajikistan Market Products
✅ BMR Preparation
We prepare product-specific, process-driven BMRs aligned with:
• Tajikistan MOH GMP requirements
• WHO GMP Guidelines
• EU GMP Guidelines (where applicable)
• US FDA cGMP (21 CFR Parts 210 & 211)
• 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 MOH & international authorities
✅ BMR Review & GMP Compliance Check
Independent technical and GMP review of existing BMRs to identify:
• Missing Tajikistan MOH / WHO GMP elements
• Documentation & data-integrity gaps
• Inspection-critical weaknesses
• Non-alignment with CIS & export-market expectations
Deliverables include clear, implementable remediation recommendations.
✅ Regulatory Query & Inspection Support
Support during:
• Tajikistan MOH post-submission queries
• MOH GMP inspections & follow-ups
• WHO audits & donor / customer inspections
• Export-market regulatory reviews
Including:
• Authority query responses
• Inspection observation remediation
• CAPA-linked BMR updates
✅ Gap Assessment & Remediation
Comprehensive gap analysis of existing BMRs against:
• Tajikistan MOH GMP requirements
• WHO GMP expectations
• PIC/S & export-market MOH requirements
With practical, floor-ready corrective actions suitable for Tajikistan-linked manufacturing 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 & export markets
Our Global Experience (Supporting Tajikistan from India)
• 3000+ BMRs prepared & reviewed
• Operational since 2008
• Experience across:
– Tajikistan
– Central Asia & CIS
– EAEU-linked markets
– Europe
– Middle East
– Asia
– 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
• Ministry of Health – Tajikistan
• WHO
• EU Authorities
• US FDA
• PIC/S Regulators
Regulatory Standards Followed
All BMR documentation is prepared in accordance with:
• Tajikistan MOH GMP Guidelines
• WHO GMP
• EU GMP (where applicable)
• US FDA cGMP (21 CFR 210 & 211)
• PIC/S GMP Requirements
• ICH Q7 / Q8 / Q9 / Q10 (where applicable)
• Country-specific MOH requirements for exports
Industries We Support in Tajikistan
• Pharmaceutical Finished Dosage Forms
• APIs & Bulk Drugs
• Sterile & Injectable Products
• Herbal & Traditional Medicines
• Nutraceuticals & Food Ingredients
• Cosmetics & Personal Care
• Industrial & Specialty Chemicals
Why Tajikistan Market Companies Choose BMRx
• 🇹🇯 Strong understanding of Tajikistan MOH & WHO GMP expectations
• 🌍 Export-oriented BMRs accepted across Central Asia & global markets
• 📋 Inspection-ready & auditable documentation
• 🔍 Reduced regulatory & 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 / packaging 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 Tajikistan manufacturers for Central Asian, CIS & global regulatory success