Walk-through GVP Modules (GVP IV) - 1 h Live Session

Hey there, are you ready to dive into the nitty-gritty of pharmacovigilance? Our interactive live session packs a punch by providing an in-depth look at the Good Pharmacovigilance Practices (GVP), specifically the fourth module. The core of this course centers on the GVP's pivotal role in ensuring medicine safety and efficacy. You'll get firsthand experience understanding how to maintain high standards of pharmacovigilance, discover the ins and outs of adverse event reporting, and dive deep into risk management plans that protect patient health.

Now, not only will you master the essential guidelines set by regulatory authorities, but you'll also see how these principles are applied in the real world. By joining this course, you're going to unlock valuable skills that will bolster your expertise in the pharmaceutical field. Whether you're a professional looking to refresh your knowledge or stepping into the world of pharmacovigilance, you'll walk away with practical know-how that can make a tangible impact on patient safety and drug development processes. So, let's get you geared up to navigate the complexities of GVP Module IV with confidence and apply these best practices to your career!

With over two decades immersed in the dynamic arena of clinical trials and pharmacovigilance, my career path has taken me through a multifaceted journey of roles, including Clinical Research Associate, Trial Site Manager, and Drug Safety Manager. These experiences have not only honed my expertise in managing global clinical trials and the post-marketing of therapeutic products but have also instilled in me a profound understanding of the unique challenges across different patient demographics and medical indications. Embracing the mantle of an EU & UK-Qualified Person for Pharmacovigilance, I've ensured the safety and efficacy of medical product life cycles, while contributing to areas such as Quality Assurance, Regulatory Affairs, and Marketing.

As the founder of ARC-Traicoa, my hands-on involvement in the industry extends to the realm of education, where I channel my passion for pharmacovigilance into cultivating the next wave of experts. Through comprehensive training sessions in Audits & Inspections, Risk Management, GVP, and Clinical Trials, I am deeply committed to empowering professionals to uphold the highest standards of patient safety and product quality. Engaging with students in this live session on GVP Modules, I aim to impart practical insights and foster a collaborative learning environment that bridges my professional insights with your academic endeavors.