Pharmaceutical Products Manufacturing: Safe, Effective & Clinically Proven
From CKD management to cardiovascular care and chronic disease treatment, our pharmaceutical manufacturing covers specialised therapeutic areas. Each product meets global pharmacopoeia standards through validated pharmaceutical production processes, ensuring consistent quality and reliability across domestic and international markets.
WHO-GMP Certified Manufacturing Excellence
Our pharmaceutical manufacturing facility in SIDCUL, Haridwar, is WHO-GMP and ISO-certified with validated drug manufacturing processes. Production includes multi-stage testing for purity, potency, dissolution, and stability per ICH guidelines, guaranteeing every batch meets international safety and efficacy standards.
Evidence-Based Formulation Approach
Our pharmaceutical manufacturing is driven by clinical evidence and patient outcomes. We develop formulations that optimise bioavailability, ease administration, and improve treatment compliance. This approach combines therapeutic efficacy with improved patient quality of life across all therapeutic categories.
Explore Our Pharmaceutical Range
Discover our comprehensive pharmaceutical manufacturing portfolio for modern healthcare needs. From acute care and chronic disease management to preventive treatment, our solutions are trusted by healthcare professionals across 50+ countries.
Pharmaceutical manufacturing is the regulated process of producing medications through formulation, processing, quality testing, and packaging under WHO-GMP standards. Eskag Pharma manufactures therapeutic formulations for chronic kidney disease, gastrointestinal health, diabetes care, and women’s healthcare, all in complete compliance with DCGI regulations.
Pharmaceutical production must comply with WHO-GMP, ISO 9001:2015, DCGI regulations, and pharmacopoeial standards (USP, BP, IP). Quality protocols include raw material testing, in-process monitoring, finished product analysis, microbial testing, and stability studies per ICH guidelines.
Drug manufacturing is the process of producing medications under regulated conditions, including API processing, dosage form manufacturing (tablets, capsules, injectables), quality testing, and packaging, in WHO-GMP-certified facilities that meet international regulatory standards.
Eskag Pharma specialises in pharmaceutical manufacturing for chronic kidney disease, gastrointestinal therapy, diabetes care, women’s healthcare, pregnancy nutrition, and topical medications. Products include tablets, capsules, sachets, syrups, creams, and ointments.
Eskag Pharma’s pharmaceutical manufacturing holds WHO-GMP, ISO 9001:2015, FSSAI, and DCGI certifications. Our facility complies with FDA guidelines, EU-GMP requirements, and pharmacopoeial standards with validated methods and complete batch documentation.