
Quality is the core foundation of Gallor Pharmaceutical Pvt Ltd. We are committed to providing high-quality pharmaceutical products that meet international standards and regulatory guidelines — ensuring every product contributes to improving patient health.
Our manufacturing partners follow strict quality control systems at every production stage — from raw material selection to final packaging. Each batch undergoes rigorous testing to maintain consistency, purity, and effectiveness.
Every product that carries the Gallor name is backed by these six non-negotiable quality commitments.
Every batch undergoes multi-point quality checks — identity testing, assay, dissolution, and microbial analysis — before release. Zero tolerance for deviation at any stage.
All facilities operate under WHO-GMP and ISO-certified environments, equipped with modern pharmaceutical-grade machinery and automated production lines.
Our manufacturing partners are DCGI-approved with valid GMP certificates, regularly audited by regulatory bodies to ensure ongoing international compliance.
Raw materials are sourced exclusively from approved, certified vendors with full Certificates of Analysis (COA) verification before any batch enters production.
Advanced quality assurance practices and in-process controls ensure every medicine is safe, therapeutically effective, and stable throughout its entire shelf life.
Our quality team regularly reviews processes, conducts internal audits, and implements CAPA (Corrective and Preventive Actions) to drive ongoing product excellence.