Celon works in niche therapy segments – a space that demands advanced manufacturing capabilities. To that end, we equip ourselves with the best-in-class technology and the best in segment practices. We adopt an approach that keeps the end customer at the centre.
Our manufacturing infrastructure enables us to comply with Indian and international regulatory requirements.
Our expertise in novel technology platforms enables in-house development of potential molecules in our focus therapy areas.
With an established product portfolio in ROW markets like LATAM, Africa, SEA, CIS etc, Celon has expertise in manufacturing formulations across a wide spectrum. We today manufacture liquid, dry powder, lipid, liposomal, polymer based microspheres and lyophilised formulations. And, we make them available in ampoules, vials and a range of oral solid dosages.
Salient features of our QMS
Facility approvals from global regulatory authorities
DIGEMID, Peru | DDA, Nepal |
FDA, Phillipines | ROSZDRAVNADZOR, Russia |
DRA, Kenya | RRFA, Ivory Cost |
NDA, Uganda |
Salient features of our QMS
INVIMA, Columbia | NAFDAC, Nigeria | NDA, Uganda |
FDB, Ghana | DRAP, Pakistan | MPH, Yemen |
PPB, Kenya | NMPB, Sudan | MCAZ, Zimbabwe |
NMRC, Namibia | MOH, Syria | MOH, Libya |
MOH, Nepal | MOH, Tajikistan | MMOH, Iran |
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