The inaugural RAPS Regulatory Conference - Europe 2020 brings together leading experts in the medical device, IVD and pharmaceutical industries to examine and provide insight on some of the most urgent and crucial issues facing regulators, manufacturers and regulatory professionals working with healthcare products for the European market.
We cordially invite all regulatory professionals and subject matter experts to Brussels, Belgium on 11–13 May, to participate in this unique gathering of stakeholders. The conference will focus on new strategies and important developments affecting regulatory professionals working in Europe’s quickly changing and uncertain regulatory environment. It is a conference created by European regulatory professionals for regulatory professionals operating in Europe, designed to foster discussion and facilitate idea exchange on these important topics.
Our volunteer committee of European regulatory experts, representing all healthcare product sectors, evaluated nearly 100 proposals to develop a timely, relevant agenda of more than 30 one-hour sessions. Sessions cover a wide range of current issues affecting the regulation and oversight of medical devices, IVDs and medicines, as well as general regulatory matters that impact all professionals in the healthcare products space.
This conference is 100% regulatory focused, developed to help increase regulatory capacity, knowledge and competency in Europe. By driving regulatory excellence and connecting the global regulatory community, we help support a thriving healthcare products sector and the advancement of public health. Join us for the 2019 RAPS Regulatory Conference – Europe and walk away with a stronger professional network, actionable insights and strategies for success.