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Quality Policy

Quality is not a department.
It is a culture.

Our commitment to quality runs through every raw material decision, every batch produced, and every shipment dispatched.

At Ramso Healthcare, quality is not inspected into our products at the end of a production line. It is built into every decision we make — from the raw materials we source, to the people we train, to the partners we choose.

We operate our manufacturing facility under WHO Good Manufacturing Practices (GMP) and hold CDSCO Drug Licence (Form 28) under the Drugs and Cosmetics Act, 1940. Our Quality Management System is certified to ISO 9001:2015 — the international standard for consistent, customer-focused quality delivery.

Our five quality pillars

01
Source quality
Every raw material is sourced from approved vendors and tested against specification before entering production. No exceptions. Our vendor qualification process ensures consistency from batch to batch.
02
Process quality
Every batch is manufactured under documented Standard Operating Procedures (SOPs). Our manufacturing records are maintained with full traceability from raw material to finished product — every step recorded, every deviation investigated.
03
Testing quality
Every finished batch undergoes in-house Quality Control testing and is released only against a Certificate of Analysis (CoA) confirming compliance with BP/IP pharmacopoeial specifications. No batch is released without passing QC.
04
Stability quality
All products are stability-tested at 40°C/75% RH per ICH Zone IVb guidelines — the standard required for tropical markets including Africa and South Asia. Our shelf life claims are based on real accelerated and long-term stability data, not assumption.
05
Supply quality
Quality does not end at the factory gate. We ensure export-grade packaging — ALU-ALU blister, amber PVC, HDPE bottles — selected specifically to protect product integrity through tropical logistics chains and long supply routes.
Our compliance standards
🏅
WHO-GMP Compliant
World Health Organisation GMP
📋
CDSCO Certified
Drug Licence Form 28
⚙️
ISO 9001:2015
Quality Management System
📘
BP / IP Grade
Pharmacopoeial standard
✅
cGMP Standards
Current Good Manufacturing Practice
🌍
ICH Zone IVb
Tropical stability testing

"We earn trust the same way we make medicine — carefully, consistently, and without cutting corners."

Request our quality documentation

WHO-GMP certificate, CDSCO drug licence, ISO certificate, and product-specific CoA available on request for verified distributors and institutional buyers.

Request Compliance Documents →