Delivering Quality Medicines
to 35+ Countries Worldwide.
From five WHO-GMP certified facilities in India, Laborate Pharmaceuticals reaches patients across Asia, Africa, the Middle East, Latin America, CIS, and Europe — backed by 400+ product registrations, dedicated export teams, and regulatory-grade documentation.
Active Across Six Continents.
Our medicines reach patients in 35+ countries — with active registrations, dedicated logistics, and in-country partners across every major emerging and regulated market.
View Regional CoverageSix Regions. Every Emerging Market.
Established operations across Asia Pacific, Middle East, Africa, Latin America, CIS, and Europe — with country-specific product registrations, dedicated logistics, and business development in each region.
Asia Pacific
12 active markets
Bangladesh, Myanmar, Sri Lanka, Nepal, Cambodia, Vietnam, Thailand, Philippines, Malaysia, Indonesia, Mongolia, Maldives
Focus: Generics, Anti-infectives, Cardiovascular, Respiratory
✓ Active — Primary Export Region
View RegionMiddle East & North Africa
8 active markets
UAE, Saudi Arabia, Oman, Kuwait, Bahrain, Qatar, Yemen, Jordan
Focus: OTC, Branded Generics, Vitamins & Supplements, Dermatology
✓ Active — High-Value Market
View RegionAfrica
7 active markets
Nigeria, Kenya, Tanzania, Uganda, Ethiopia, Ghana, Zimbabwe
Focus: WHO-PQ Generics, Anti-malarials, Anti-infectives, Maternal Health
✓ Active — Growth Region
View RegionLatin America & Caribbean
5 active markets
Colombia, Peru, Ecuador, Bolivia, Dominican Republic
Focus: Generics, Respiratory, Gastrointestinal, Dermatology
✓ Active — Expanding
View RegionCIS & Central Asia
5 active markets
Kazakhstan, Uzbekistan, Kyrgyzstan, Tajikistan, Turkmenistan
Focus: Generics, Cardiovascular, Neurological, Anti-infectives
✓ Active — Established
View RegionEurope
3 active markets
United Kingdom, Germany, Romania
Focus: EU-GMP Ready, Specialty Generics, Regulated Market Dossiers
✓ Active — Expanding
View RegionEnd-to-End International Capability.
From freight and documentation to regulatory filings and serialisation — our dedicated export infrastructure covers every step of getting quality medicines to patients worldwide.
International Logistics
Multi-modal freight solutions — air and sea — with 98.2% on-time dispatch rate. DDP, DAP, and FOB terms available for all major Incoterms.
Export Documentation
Complete export documentation — COA, Certificate of Free Sale, GMP certificates, regulatory dossiers, and country-specific import permits.
Regulatory Compliance
WHO-GMP certified facilities, PIC/S-aligned quality systems, and pre-approval inspection readiness for USFDA, EU, and regulated market submissions.
Serialisation & Track-Trace
GS1-compliant serialisation, 2D barcode printing, and aggregation for EU Falsified Medicines Directive, DSCSA, and country-specific track-trace requirements.
Cold Chain Management
Temperature-controlled logistics for cold-chain products — 2–8°C integrity maintained from manufacturing to destination, with GDP-compliant documentation.
Export Packaging
Market-specific label printing, multi-language patient leaflets, and complete artwork management — compliant with destination country labelling regulations.
Compliance Recognised Worldwide.
Our manufacturing certifications and regulatory standing open doors across every major pharmaceutical market — from emerging to fully regulated.
WHO-GMP Certification
All five manufacturing facilities hold WHO-GMP certification — the international benchmark for pharmaceutical quality, safety, and efficacy.
ISO 9001:2015
ISO 9001:2015 certified quality management system — demonstrating consistent, internationally audited quality processes across all operations.
PIC/S Guidelines
Manufacturing aligned to Pharmaceutical Inspection Co-operation Scheme (PIC/S) GMP guidelines — accepted in 46 member countries including EU, Australia, and Canada.
USFDA Readiness
Pre-approval inspection ready facilities with ANDA filing capability. Internal quality systems and documentation aligned to 21 CFR Parts 210 and 211.
EU-GMP Documentation
Quality dossiers prepared in Common Technical Document (CTD) format to EMA and EU-GMP standards — supporting regulated market registrations across Europe.
Country Registrations
Over 400 product registrations across 60+ markets — with active pipeline for new registrations in priority emerging and regulated markets.
Why International Partners Choose Laborate.
Trusted by distributors, healthcare companies, and government bodies across 35+ markets for consistent quality, reliable supply, and dedicated support.
Reliable Global Supply
Dedicated Export Team
Technical & Scientific Support
Regulatory Dossier Assistance
Flexible Batch Sizes
WHO-GMP Quality Assurance
98.2% On-Time Dispatch Rate
Dedicated Key Account Manager
Trusted by Partners Across the World.
From East African institutional supply to GCC branded generics and Latin American WHO-PQ exports — real outcomes with real international partners.
East Africa
Regional Healthcare Distributor
"Consistent quality, reliable documentation, and on-time delivery make Laborate our preferred long-term manufacturing partner for the East African institutional market."
Middle East — GCC
International Pharma Brand
"Laborate's dedicated export team handled all UAE and KSA registration documentation in parallel — our products reached shelves 4 months ahead of our previous supplier's timelines."
Latin America
Pharmaceutical Distributor
"The regulatory support from Laborate's export team was exceptional — INVIMA submissions, Spanish-language labelling, and GDP-compliant freight in a single workflow."
International Business
Ready to Take Your Business Global?
Connect with our International Business Development team. We help distributors, brands, and institutions build reliable, compliant pharmaceutical supply chains across every major global market.
Speak with Our International Business Team
Enquiries handled by regional export specialists — not a contact form. We respond within one business day.