WHO-GMP Certified Pharmaceutical Supplier for Latin America from India

Countries We Supply in Latin America

• Venezuela — Anti-infectives, cardiovascular, analgesics, vitamins
• Guatemala — Tablets, capsules, dry syrups, liquid orals
• Dominican Republic — Full range of generic formulations
• Honduras — Anti-infectives, paediatric formulations
• El Salvador — Tablets, capsules, syrups
• Nicaragua — Essential medicines, anti-infectives
• Ecuador — Generic tablets, capsules, liquid orals
• Bolivia — Full therapeutic range

Why Latin American Importers Source from Lucent Biotech

• WHO-GMP Certification — Accepted by health ministries and regulatory agencies across Latin America as proof of GMP compliance
• Competitive Pricing — Indian manufacturing costs are among the lowest globally for WHO-GMP quality medicines
• Complete Documentation — We provide CPP (Certificate of Pharmaceutical Product), COA, SMF, stability data, and product dossiers required for registration in your country
• Spanish-Language Support — Our team can communicate and provide product labelling support for Spanish-speaking markets
• Flexible Pack Sizes — Blisters, bottles, strip packs — customised to your market’s standard presentation

Products for Latin American Markets

Most Demanded Categories

• Anti-Infectives — Amoxicillin, Ciprofloxacin, Azithromycin, Metronidazole, Doxycycline (tablets, capsules, dry syrups)
• Analgesics / Antipyretics — Paracetamol, Ibuprofen, Diclofenac
• Cardiovascular — Amlodipine, Atenolol, Losartan, Metformin
• Gastro-Intestinal — Omeprazole, Pantoprazole, ORS sachets
• Vitamins & Supplements — Multivitamins, Vitamin C, Iron + Folic Acid, B-Complex
• Antihistamines — Cetirizine, Loratadine
• Paediatric Formulations — Dry syrups, suspensions, paediatric drops

Regulatory Support for Latin America

We provide the following documents required for pharmaceutical product registration in Latin American countries:

• WHO-GMP Certificate of Pharmaceutical Product (CPP) — CDSCO issued
• Free Sale Certificate (FSC)
• Certificate of Analysis (COA) — batch-wise
• Site Master File (SMF)
• Stability Study Data (accelerated + real-time)
• Full CTD/ACTD format dossier support
• Notarisation and apostille support as required

Our Certifications

• WHO-GMP Certified Manufacturing Facility (Roorkee, Uttarakhand, India)
• ISO 9001:2015 Quality Management System
• CDSCO Drug Manufacturing Licence
• Pharmexcil Member