From a single vision in 2004 to a globally certified biopharmaceutical CRDMO serving markets across four continents — the Bioplus journey is one of relentless innovation and scientific commitment.
Bioplus Life Sciences was founded in 2004 in Bangalore, India, with a clear mission: to build an integrated, science-first pharmaceutical company capable of competing on the world stage. From the very beginning, the focus was on quality, compliance, and a deep respect for the complexity of drug development.
Over the following two decades, Bioplus expanded steadily — investing in fermentation infrastructure, formulation capabilities, and the regulatory approvals needed to serve regulated markets in the UK, Europe, Australia, Canada, and beyond.
Today, Bioplus is an integrated cGMP biopharmaceutical CRDMO with three production facilities, 400+ employees, 100+ scientists, and a track record of delivering for some of the world's most demanding pharmaceutical partners.
Key moments that shaped Bioplus into the integrated CRDMO it is today. Hover over each milestone for details.
EU GMP
Halal Certified
TGA
Health Canada
UNICEF
MHRA
NABL
SMETA / SEDEX
C-TPAT
SSCI
Our culture of scientific excellence and commitment to quality shapes everything we do.
Pioneering next-generation manufacturing through precision fermentation, metabolic engineering, and synthetic biology platforms.
Every product meets the highest global regulatory standards — UK MHRA, EU GMP, TGA Australia, and Health Canada.
State-of-the-art OSD manufacturing facility offering end-to-end capabilities from formulation development to commercial-scale production of tablets, capsules, powders, sachets, and effervescent dosage forms.