Quality is not a department.
It is the foundation everything else stands on.
At RB Remedies, the quality of a medicine is not measured by what it claims on the label. It is measured by what it does on the 10,000th batch, the 100,000th patient, and the 24th month on the shelf.
Our quality systems are designed to deliver consistency across all three.
Every product in our portfolio is manufactured in facilities certified to WHO-GMP standards, with quality oversight that begins at raw-material screening and continues through in-process control, finished-product release testing, and long-term stability studies aligned with ICH guidelines.
01.
Raw Material Integrity
Every incoming API and excipient is tested for identity, purity, and potency before being approved for production — without exception, without shortcut.
02.
In-Process Control
Quality oversight runs throughout the manufacturing cycle, not just at the end. Multi-stage IPQC ensures every tablet, every capsule, every vial meets specification.
03.
Finished Product Release
No batch leaves the facility without complete analytical testing — assay, dissolution, disintegration, microbial limits, and packaging integrity.
04.
Stability & Shelf Life
Long-term and accelerated stability studies confirm that what works on day one continues to work on the last day of shelf life — under Indian climatic conditions.
Externally verified — not self-attested.
ISO 9001:2008
JAS-ANZ Accredited
Validity: Current
CRISIL Rating
CRISIL Ratings Ltd.
Validity: Annual
WHO-GMP Compliance
Manufacturing Facility
Validity: Current
Drug Manufacturing Licence
FDCA, Gujarat
Validity: Current
GST Registration
Govt. of India
Validity: Active
PHARMEXIL Membership
Pharma Export Council
Validity: Current
"We do not promise perfection. We promise process — repeated honestly, every single time."