In this webinar, Dr Steffen Thirstrup and Professor Carole Longson will explore the steps that can be taken to develop and communicate a compelling, evidence-based value story.
Today we shine the spotlight on Hildegard Schmatz. Hildegard specializes in European regulatory procedures including linguistic reviews and lifecycle activities, regulatory project management as well as regulatory planning and QC management.
In this webinar Dr Roz Cox will discuss the many opportunities that exist to interact with European Regulatory Agencies during product development to optimise Regulatory submissions.
Your drug development needs are unique
Contact us to learn how our experts can support you to meet all regulatory, quality and safety requirements and ensure the best path to approval.
Let's Bring Medicines to the World