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The company has since 1998 a quality system ISO 9000 in actual version 2015 certified by AENOR. Actually we are in process to get certification of ISO 14001 and ISO 15378 (GMP pharma).

All our pharmaceutical production is packed in pressurized clean room with laminar flow and access with double automatic lock system. The clean room is formaly qualified ISO 7 according to UNE-EN ISO 14644-1.

During the production we adapt to the quality specifications defined by our customers or if no special requirements is defined, we use our own specification based in ISO 2859-1.

Cosmetic control and micro cracks detection with camera ( Japan quality ) upon demand.

Possibility of delegated sampling.

In house laboratory to perform hydrolytic resistance test according to most known pharmacopoeias (EU, USA or Japan) during all the production.

Several functional tests before release (vertical pressure, break tester, vacuum, etc ..

Quality policy
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