Walk-through GVP Modules (GVP Module III) - 1 h Live Session

Dive right into the heart of Good Pharmacovigilance Practices with our engaging 1-hour live session crafted to give you the ins and outs of GVP Module III. If you've been curious about how medicinal products are kept safe and effective throughout their lifecycle, this is your golden chance! We're unpacking the essential guidelines that govern the safety, quality, and risk management of pharmaceuticals. Not only will you grasp the module's key principles, but you'll also learn how to apply them in the context of the real-world pharmacovigilance system.

Now, let's talk application: it's not just about theory, right? You'll leave this session equipped to weave GVP Module III into your professional toolkit. Whether you're in the pharmaceutical industry, healthcare, or a regulatory agency, you'll find this content incredibly valuable. Understanding these guidelines means you can help ensure the well-being of patients and the integrity of medical treatments. So, ready to up your game and make an impact? Let's do this!

With over two decades of dedicated service in the realm of clinical trials and the post-marketing of medicinal products, I bring a wealth of expertise to this course on Good Pharmacovigilance Practices. My extensive background includes multi-faceted roles such as Clinical Research Associate, Trial Site Manager, and Drug Safety Manager, overseeing global clinical trials and post-marketing activities across diverse indications and patient demographics. As an EU&UK-Qualified Person for Pharmacovigilance, I have a panoramic view of product lifecycle management, expertise in compliance, and a profound understanding of European pharmaceutical law – knowledge I am eager to pass on to my students.

Founding ARC-Traicoa reflects my devotion to the field of pharmacovigilance, creating a hub for comprehensive support in this critical aspect of healthcare. I pair this hands-on experience with a passion for education, regularly providing training on Audits & Inspections, Risk Management, GVP, and Clinical Trials. My goal is to equip you with the practical skills and insights needed to excel in your pharmacovigilance career, fostering a learning environment that bridges theoretical knowledge with real-world applications.