The deviation management process is a requirement and is designed to be a part of the Quality Management System (QMS) imposed by all major GMP.
Method development as a key process to encompasses the process of establishing chemical analytical techniques.
How to register a generic medicine in the European market?
Signal management is complex and requires a customized approach to each product. Read this article to optimize your signal management strategies with.
Are you looking to expand your drug products into the European market? Let us guide you through the process with a detailed overview.
Are you interested in learning about stability studies and their critical role in the manufacturing process of new products?
A number of processes must be completed by the manufacturing company in order to receive EU certification for its product. Are you aware of them ?
Read insight from our expert to learn more about most important aspects of technology transfer processes in the pharmaceutical landscape.
Cleaning Validation for Biotech products: our expert Marco Paolillo addresses the main challenges in the process.
Cleaning Validation in the Pharmaceutical Industry: our expert Marco Paolillo addresses the 5Wsv to avoid contamination and cross-contamination.
