Gamp 5 Version 2 released in July 2022 brings new updates for computerized systems in the Life Science industry.
Are you ready to implement the EU ISO IDMP standards for medicinal products? Discover with us how to safely move to the new standards
The Ministry of Health of Israel has just been included in the Medical Device Single Audit Program (MDSAP), what are the changes?
Cleaning Validation in the Pharmaceutical Industry: our expert Marco Paolillo addresses the 5Wsv to avoid contamination and cross-contamination.
Effective June 30, 2022, the registration procedure for Food Supplement notification in Italy has changed.
Regulated companies are moving to Cloud solutions to store data, improving their performance and capability, while keeping a careful GxP oriented.
Stephen Tyrpak, Executive Consultant @ PQE Group speaks about how to raise funds for your start up in the Life Science Industry.
Many countries are working to implement or improve their Tobacco risk reduction policy, to ensure a lower rate of diseases and deaths connected to.
Last decade has witnessed an increasing interest in the Cannabis field considering every aspect, from business applications to more scientific and.
Vaccine Technology Transfer is a core challenge for pharmaceutical companies that are involved in the fight to Covid-19.
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