Regulatory, QA and PV


Local knowledge, professional and qualified relations with health authorities can make a valuable difference.

Speed and short time lines will often bring you faster to the market  – or restore regulatory/QA challenges blocking your sales.

GxMed Nordic’s staff is highly qualified and capable of handling regulatory and quality issues. From help to submitting a variation, to establish QA systems and to obtain a GDP or GMP license. We think out of the box, to optimize faster handling of projects, without compromising regulatory standards.

PV is in the process of being developed for internal handling. Meanwhile we have consultants at hand.

The combination of close relations with the authorities and our way of working generates valuable results.

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