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Irene Lanza
Regulatory Affairs Manager at GSK
Professional Background
Irene Lanza is a highly skilled professional with extensive experience in the field of regulatory affairs, particularly dedicated to the oral health sector. She currently serves as the Regulatory Affairs Manager for Oral Health at GlaxoSmithKline (GSK), where she applies her expertise to ensure compliance with both internal and external regulations. Her role is pivotal in navigating the complex landscape of product approvals and ensuring that the company's oral health products meet the highest standards of safety and efficacy. Irene’s leadership at GSK reflects her commitment to enhancing consumer trust and product reliability in a competitive market.
Prior to her role at GSK, Irene held several prominent positions that have contributed to her well-rounded expertise in regulatory affairs. She was a Product Certification Specialist in Medical Devices at Certiquality Srl, where she honed her understanding of medical product standards and certification processes. This role provided her with valuable insights into the critical evaluation of medical devices and their market compliance.
Irene's career also includes experience as an International Regulatory Affairs Specialist at Mylan, where she developed strategies for navigating regulatory challenges across various international markets. Her responsibilities included maintaining awareness of legislative changes, which is crucial in ensuring timely market access for products.
Additionally, Irene has worked as a Regulatory Affairs Specialist Consultant at Pharma D&S, a firm known for its consultancy in pharmaceutical regulatory matters. During her time there, she leveraged her analytical skills to drive successful outcomes for her clients, showcasing her proficiency in regulatory framework navigation. Starting as a Junior Consultant in the same company, she built a foundational understanding of regulatory processes that set the stage for her impressive career trajectory.
Irene’s journey began as a Trainee at Farmacia Ninci, where she first developed a passion for the pharmaceutical industry. This early experience laid the groundwork for her pursuit of a career dedicated to ensuring that healthcare products adhere to essential safety regulations.
Education and Achievements
Irene Lanza received her Master’s Degree (MSc) in Chimica e Tecnologia Farmaceutiche from the prestigious Università degli Studi di Firenze. This academic background equipped her with deep scientific knowledge and advanced technical skills necessary for a successful career in pharmaceutical and regulatory affairs. Her education focused on critical aspects of pharmaceutical chemistry and technology, providing her with a robust understanding of drug formulation, safety assessment, and compliance.
Irene's combination of rigorous academic training and extensive professional experience makes her a leading expert in regulatory affairs, particularly in oral health and medical devices. Her work has contributed significantly to the formulation and governance of products that improve patient care and health quality.
Achievements
Throughout her career, Irene Lanza has achieved numerous milestones that underscore her expertise and dedication to the regulatory affairs field. Her ability to lead projects at GSK has been instrumental in the successful launch of several oral health products, enabling the company to address consumer needs effectively.
Irene's contributions go beyond project management; she has played a vital role in developing strategies to meet new regulatory requirements, ensuring that GSK adapts swiftly to the evolving landscape of healthcare regulations.
Moreover, her experience across various organizations has given her a unique perspective on regulatory compliance, making her a sought-after resource for guidance on complex regulatory issues. Irene's ability to communicate effectively across diverse teams has been crucial in fostering collaboration and ensuring that regulatory considerations are integrated throughout the product development cycle.
Irene Lanza's impressive background in regulatory affairs, combined with her academic credentials, positions her as a leading professional in her field. Her commitment to excellence and deep understanding of pharmaceutical regulations are assets to any organization in the healthcare sector.