We are seeking experienced regulatory affairs professionals with a specialization in medical devices to volunteer as subject-matter experts (SMEs) to help RAPS develop a new eLearning course on navigating pre-application meetings for devices.
This course is designed to empower regulatory professionals worldwide with the knowledge and strategies to engage effectively with regulatory agencies. As an SME, you will collaborate with our team to help write content, validate content accuracy, provide real-world insights, and ensure that the course addresses the practical needs of professionals preparing for critical pre-application discussions.
Your contributions will directly impact the effectiveness of the course and the success of its participants in navigating the complex regulatory environment. The ideal volunteer is someone with proven expertise in the regulatory affairs sector for medical devices, and a familiarity with the pre-application processes of major regulatory agencies.