List view / Grid view
The European Regulatory Framework for Medical Device field is changing with the release of the new Regulation. The MDR will replace the existing Directives and it will be fully in force in May 2020.
This booklet from PQE Group is your opportunity to learn how the new EU directives - EU MDR 2017/745-746 - affect your company. Read on to find out what preparations you can make to ensure that your products comply.
At PQE Group we foster innovation, efficiency and quality services for sustainable regulated compliance solutions.
Regulatory expectations nowadays focus on harmonisation of global regulations. This whitepaper by PQE looks at current and emerging trends in regulatory expectations.
21 March 2019 | By
Complete quality solutions provider for Life Science since 1998: a global coverage for Data Integrity Services, GxP Compliance, Technical Qualification, Third Party Audits and Regulatory Affairs.
The counting of votes that saw the election of Mr. Claudio Puglisi, new COO of PQE Group, was held last January 31st in Milan, Italy...
Find out more about PQE Group services from our Vice President and Partner Danilo Neri at last PharmaLab 2018 in Dusseldorf.
Improving data integrity is the aim of a new guide published by the Russian State Institute for Drugs and Good Practices in collaboration with consultancy PQE Group...
