At the end of April 2023, the EU Commission announced the largest reform of the pharmaceutical sector in over 20 years. Why is this happening right.
Pharmacovigilance System Master File (PSMF), describes the details of the pharmacovigilance system, focusing on the Quality Management System (QMS).
The European Medicines Agency (EMA) has issued guidelines for the environmental risk/impact assessment (ERA or EIA) of veterinary medicinal products.
Pharmacovigilance system for the Veterinary Industries and that the compliance to the requirements requested by the EU regulations.
The Committee for Veterinary Medicinal Products has released a new guideline on the prescription status of veterinary medicinal products.
In January 2023, the implementation of risk assessment requirements to control elemental impurities in veterinary medicinal products will enter into.
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 Life Science industry revolution goes along with the development of data interoperability systems that allow shared data within the entire.
Effective June 30, 2022, the registration procedure for Food Supplement notification in Italy has changed.
EMA has recommended the suspension of around 100 generic drugs for Data Integrity and Reliability issues, with the consequence of repeating the.
