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Inzign is staffed with a team of professionals with proven knowledge and track records in process validation for FDA cGMP compliant 21 CFR Part 820. The Company’s manufacturing facilities include three Class 100,000 clean rooms and one Class 10,000 clean room located in Singapore and Indonesia which are ISO 9001:2000 and ISO 13485:2003 certified. Inzign's partners are multinational OEMs from US, Europe and Japan, in the disposable medical devices, pharmaceuticals related devices, and diagnostics industries. Some of the therapy areas where we have developed capabilities are in haemodialysis, medication management, drug delivery, diagnostic kits and related devices
SG 16 kallang place
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