CGMP Complied, Validated Clean Room facility with latest equipment

Products comply with USP, EP, BP,JP & other regulatory standards

Access to Large Device Design Database

High level documentation support for ‘CE’ Marking, Canadian & US DMF, US FDA 510(k), 21CFR 820

IPR Protection Guaranteed – many patents are filed

Dedicated Innovative Product Development team

In-house Molding Making and Micro Moulding facility for quicker Development and sample generation