Veol Labs is an ISO 13485 certified medical devices development company, based in India, providing any and all services in the product life cycle from concept to commercial launch. USA FDA QSR and CE requirements for design control are strictly followed enabling the clients to get faster regulatory approvals. Veol is among few Indian companies serving the medical device community. Veol employ talented, world class professionals who are specialists in the Design, Development, Validation and Manufacture of Class II and Class III therapeutic, diagnostic and surgical devices. Having a history of demonstrated cost leadership, Veol Labs clients typically save 70% to 75% of product development costs.

Veol’s Services include -

• Concept Generation – Multidisciplinary team, TRIZ, 6 Hat, Ethnography
• Industrial Design – Styling, User Interface, Mock modeling
• Prototyping – FRP, SLA, SLS, FDM, Machining & Fabrication
• Product Development – As per ISO 13485 and US FDA QSR guidelines
• Pilot Manufacturing – Clean room manufacturing and assembly
• Product Validation Services – As per ICH-GCP guidelines, in alliance with Karmic Lifesciences
• Clinical Literature search and review services
• R & D and Patent filing