CanBio Pharmaceuticals LLP is registered and certified for complying with CDSCO, FDCA, C-GMP, GLP, ISO 9001-2015, ISO 14001-2015, ISO 45001-2018 & WHO – GMP and cutting-edge infrastructure that offers smooth process development and manufacturing services. Our enterprise occupies 1500 sq mtr. with all requisite facilities and well equipped instrumental, Physicochemical and micro-lab is matching with USFDA and EU Permitted Units. All the testing facilities are available in-house.
Also our unit having highy equipped in-house quality control lab like Physico chemical lab, Instrument lab and Microbiological lab.
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GMP
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CDSCO
Central Drugs Standard Control Organization -
FDCA and C-GMP, GLP
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WHO – GMP
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ISO Certificate
Key Features
- Totally automated unit with electronically controlled operating system as per good manufacturing practice (GMP) guidelines.
- Contemporary Microbiological, QA, QC, and Physio Chemical Lab propped up with high-tech equipment.
- Refined effluent treatment plant (ETP) for sustainable environment with a vast capacity.
- Comply with international environmental, health and safety regulations.