In a rapidly evolving regulatory landscape, health and beauty brands face increasing scrutiny. Whether it's a food supplement promising enhanced wellness or a cosmetic product offering skin rejuvenation, regulatory compliance is no longer optional—it's a critical component of successful market entry and long-term brand integrity.
In the ever-evolving landscape of pharmaceuticals, patient safety remains paramount. This is where Pharmacovigilance (PV) services step in
A Qualified Person for Pharmacovigilance is an individual residing within the European Economic Area (EEA), who is personally responsible by law for the safety of a human pharmaceutical product within the EEA
In the pharmaceutical industry, drug safety is paramount. Ensuring that medications are safe for patients involves rigorous testing and ongoing monitoring, even after a drug has been approved and released to the market. One crucial aspect of this post-market surveillance is medical literature monitoring (MLM). Effective MLM can streamline drug safety processes, ensuring that adverse effects are identified and addressed promptly. This article explores the importance of MLM in drug safety, the challenges faced, and best practices for implementing a robust MLM system.
