Targeted regulatory dossiers, packaging compliance, and logistics pipelines tailored to national Health Ministries and commercial drug authorities.
Authority: NAFDAC (National Agency for Food and Drug Administration and Control)
Supplying high-demand allopathic generic formulations and pediatric oral liquids to Nigerian pharmaceutical im...
Authority: Pharmacy and Poisons Board (PPB), Kenya
A trusted Indian pharmaceutical export partner providing finished formulations, chronic disease medicines, and...
Authority: Food and Drugs Authority (FDA), Ghana
Delivering high-efficacy finished pharmaceutical products, pediatric antibiotics, and chronic therapies to lic...
Authority: Tanzania Medicines and Medical Devices Authority (TMDA)
Supplying essential medicines, oral solids, pediatric liquids, and hospital injectables to licensed Tanzanian ...
Authority: Standards and Regulation Division, Ministry of Health & Wellness, Jamaica
Connecting Jamaican pharmaceutical distributors, community pharmacy chains, and institutional buyers with high...
Authority: Pharmacy Council of Saint Lucia & Ministry of Health, Wellness and Elderly Affairs
A dedicated pharmaceutical sourcing bridge for Saint Lucian importers, OECS pooled procurement tenders, and Ea...
Authority: Chemistry, Food and Drugs Division (CFDD), Ministry of Health, Trinidad and Tobago
Delivering WHO-GMP certified oral solids, liquid orals, and specialized therapies to licensed Trinidadian phar...
Authority: Department of Drug Administration (DDA), Nepal
Accelerated overland pharmaceutical supply to Nepali importers, Kathmandu distributors, and hospital supply ch...
Authority: Food and Drug Administration (FDA), Philippines
Providing high-quality generic medicines, ASEAN Common Technical Dossiers (ACTD), and contract manufacturing t...
Authority: Ministry of Health and Prevention (MOHAP), UAE
High-standard pharmaceutical formulations, private-label hospital supplies, and regional re-export solutions f...
Manufactured in certified WHO-GMP partner suites adhering to British (BP), United States (USP), and Indian Pharmacopoeia (IP) standards.
Film coated, enteric coated, dispersible, effervescent & bilayer tablets in high-barrier ALU-ALU and blister packs.
Explore Technical Specs →Enteric sustained-release pellets (DSR/LSR), multi-ingredient vitamins, and vegetarian HPMC capsule options.
Explore Technical Specs →Pediatric suspensions, cough syrups, antacids, and multivitamin liquids in amber PET bottles with measuring caps.
Explore Technical Specs →Antibiotic dry suspensions (Amoxicillin-Clav, Cefixime) supplied with sterile Water for Injection (WFI).
Explore Technical Specs →Critical care cephalosporins, carbapenems, and liquid vials/ampoules manufactured under ISO Class 5 cleanroom conditions.
Explore Technical Specs →Antifungal creams, steroid ointments, antibacterial gels, and medicated lotions in seamless laminated tubes.
Explore Technical Specs →FSSAI/GMP certified protein powders, nutritional gummies, multivitamin effervescent tablets, and softgel supplements.
Explore Technical Specs →End-to-end overseas brand customization, artwork design, regulatory file preparation, and batch export dispatch.
Explore Technical Specs →Airtight statutory files prepared by our in-house regulatory affairs team to ensure expedited product licensing in your jurisdiction.
Issued by CDSCO / State Licensing Authority under the international WHO Certification Scheme on the quality of pharmaceutical products moving in international commerce.
Official certification from the statutory drug licensing authority confirming that formulations are freely sold and distributed in the country of origin.
Comprehensive Module 1 through Module 5 technical documentation (Administrative, Quality Overall Summary, Chemical & Pharmaceutical Quality, Non-Clinical, and Clinical Study summaries).
Batch-specific chemical assay, dissolution profile, HPLC chromatography, and microbial testing reports accompanied by official Methods of Analysis.
Accelerated (40°C ± 2°C / 75% RH ± 5% RH) and long-term (30°C ± 2°C / 75% RH ± 5% RH) stability testing confirming real-world efficacy in hot and humid tropical export destinations.
Verified quality management documentation from manufacturing facilities adhering to Revised Schedule M and WHO standards.
Engineered for maritime turbulence resistance, container heat tolerance, and zero-defect customs clearance.
Heavy-duty 7-ply export-worthy corrugated master shippers designed for maritime and air turbulence resistance.
Tropical climate cold-formed ALU-ALU foil and 90gsm PVDC barrier coatings preventing moisture ingress in high-humidity markets.
Heat-treated ISPM-15 compliant wooden/plastic pallets with four-way entry, corner board protection, and heavy stretch wrapping.
Air cargo via Delhi Indira Gandhi International Airport (IGI / DEL) & sea container freight via Nhava Sheva (JNPT Mumbai) and Mundra Sea Ports.
Transparent milestone tracking from initial formulation selection to container loading.
Submit target compositions, strengths & estimated volume.
Receive Proforma Invoice with FOB/CIF rates within 24 hours.
Receive COPP, FSC & CTD files for local MOH registration.
Formulation in WHO-GMP plant with custom export packaging.
Air / Sea freight handover with certified Batch COA & Bill of Lading.
Essential answers for international medicine importers, distributors, and hospital sourcing agents.
Yes. We provide complete private-label contract manufacturing for international distributors, including customized brand artwork, bilingual regulatory packaging cartons, and dedicated batch production.
We supply complete ACTD (ASEAN) and CTD dossiers (Modules 1 through 5), including Certificate of Pharmaceutical Product (COPP), Free Sale Certificate (FSC), Certificate of Analysis (COA), Method of Analysis (MOA), process validation files, and Zone IVb stability reports.
Initial production runs with custom-printed export foil and cartons require 35 to 45 days upon artwork and regulatory sign-off. Repeat orders are dispatched within 20 to 25 days ex-factory.
We support standard international commercial terms including Ex-Works (EXW), Free On Board (FOB Mumbai / FOB Delhi), Cost and Freight (CFR), and Cost, Insurance, and Freight (CIF) to your designated destination seaport or international airport.
All export batches are formulated and packaged at certified WHO-GMP partner plants (such as Akums, Windlas, Biodeal, Ultra Drugs, Medicef, Mascot). Importers are welcome to conduct on-site factory audits or video-audits accompanied by our technical liaison team.
