ExpertFORUM Labelling

Senior Director and Project Lead for Gravitate Health; Giovanna Ferrari is a Senior Director, Regional Labeling Lead at Pfizer. She holds a PhD from University College London and has over 20 years' experience in pharmaceutical regulatory affairs. She has a strong background in labeling and product information, having specialized in this area since 2009, and is the global business process owner for the Pfizer process for management of country labeling documents. Externally, Giovanna has represented Pfizer in a wide range of industry forums over the last few years, in particular focussing on e-labelling, and is the industry lead for a highly innovative and patient-focussed digital health information project that is being progressed via an IMI public-private partnership - Gravitate-Health.

Head of Global Labeling Operations & Digitization; Dr. Jänich is an expert in Regulatory Affairs with extensive expertise in the field of labeling. In his role, he is responsible for the labeling process as well as associated systems, compliance, and digitalization. Furthermore, he advances the development and implementation of Structured Content Authoring and electronic product information in the GxP-regulated environment.

Regulatory Nets Lead; Tris leads the industry Regulatory Networks (labelnet & rimnet) at Navitas Life Sciences. With over 20 years of experience in the Healthcare industry, Tris has a strong background in Labeling, Regulatory, Quality Management and the underlying technologies. She is committed to advancing industry best practices, particularly in the E2E labeling processes and is always seeking opportunities to balance the demands of patients and regulators alongside industry working practices.

Julian has been working at IQVIA before starting his own consultancy. During his tenure with IQVIA Technology SRQ (Safety, Regulatory and Quality) Julian has lead a dynamic team responsible for the design and development of IQVIA’s label information, content management and authoring solution. Focused on the complex challenges of the core, local and regional label change process.

Senior Adviser Product Information, QRD member, CMDh alternate; Nina Malvik is a Senior Adviser at the Norwegian Medicines Agency. With 13 years of experience in regulatory affairs, Nina Malvik has a strong background in product information. She is committed to safe and correct use of medicinal products and is always seeking opportunities to improve the ways of communication between the parties involved. Previously, she worked as a pharmacist at Adler Apotheke, Wandsbek, Hamburg where she gained valuable experience in production of sterile and non-sterile medicinal product as well as informing and educating patients and healthcare personnel in all aspect related to correct and safe use of their medicine. Nina Malvik holds MSc from University of Hamburg, Germany. She is passionate about medicinal communication and is dedicated to making communication of safe and correct use of medicinal products fit for the future.