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GXP ©Copyright. All rights reserved
GXP – expert agency
We provide consulting services concerning:
- certification and marketing of medical devices (MD);
- good manufacturing practice (GMP) in the field of diagnostic audits (including API manufacturers), staff training and compliance;
- good distribution practices (GDP) in the field of diagnostic audits, staff training and compliance.
GXP is a competent and reliable regulatory partner to ensure a success of your company on the EU medical device market
Services
GXP is a competent and reliable regulatory partner to ensure a success of your company on the European Union and the Commonwealth of Independent States medical device market
GXP is a competent and reliable regulatory partner to ensure a success of your company on the European Union and the Commonwealth of Independent States medical device market
- We operate with a reliable information only.
- We provide services on the highest level.
- We involve the most competent advisors.
- We work on the bases of effective law only.
- We work with reliable companies only.
Why GXP?
- We are a team of experts with a broad experience of work in medical devices regulation.
- We irreproachably know requirements of national and European legislation.
- We provide services on a turnkey basis
GXP by numbers
GXP’s mission – to facilitate the process of medical devices legalization and to create a legal way for new players to enter the EU and CIS market of medical devices, which in general will lead to qualitative changes in the market.
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CONTACTS
ul.Lubicz 27/40, 31-503
Krakow, Poland
+48 1225 44 831
+48 6906 25 630
info@gxp-europe.com
Our competence
We are a team of experts with a broad experience in medical devices (MD) regulation (MD), good manufacturing practice (GMP), good distribution practice (GDP). We know irreproachably requirements of the national and European legislation.
CONTACTS
ul.Lubicz 27/40, 31-503
Krakow, Poland
+48 1225 44 831
+48 6906 25 630
info@gxp-europe.com