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The regulatory function is vital in making safe and effective healthcare products available worldwide. Individuals who ensure regulatory compliance and prepare submissions, as well as those whose main job function is clinical affairs or quality assurance are all considered regulatory professionals.
Resources, news and special offers to support you and your professional development during this difficult time.
One of our most valuable contributions to the profession is the Regulatory Code of Ethics. The Code of Ethics provides regulatory professionals with core values that hold them to the highest standards of professional conduct.
Your membership opens the door to free learning resources on demand. Check out the Member Knowledge Center for free webcasts, publications and online courses.
Like all professions, regulatory is based on a shared set of competencies. The Regulatory Competency Framework describes the essential elements of what is required of regulatory professionals at four major career and professional levels.
Download your copy of the new events calendar and see all the online workshops, conferences, RAC exams and European online workshops RAPS has planned for 2021 at a glance.
An invaluable resource for any professional engaged in designing, composing, compiling, or commenting on regulatory documentation
From self-assessments to help you identify your strengths and areas to focus on to reference books and online courses that will help you fill in the gaps in your regulatory knowledge, RAPS has the resources to help you prepare for the RAC exam.
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Member: FREENonmember: FREEYour participation in the regulatory community is vital. The RAPS European Council (REC) is offering this webcast for free so that global regulatory professionals maintain access to valuable knowledge about issues currently impacting our industry.DescriptionWith the European Commission making the Actor module of EUDAMED available on a voluntary basis from 1 December 2020, we will focus this presentation and discussion to provide you with an overview of the current status of implementation and launch. This webcast will focus on practical information and tips specific to the Actor Registration module, and will address why cross-functional collaboration and data organisation are so important in relation to EUDAMED and process rationale for your Notified Body. A Q&A session will be provided at the end. This event is brought to you by the RAPS European Council (REC) to encourage knowledge sharing and community development. RAC holders may claim 1.0 RAC recertification credit. Learning Level: BasicBasic: Content is introductory in nature and requires no requisite knowledge or experience to grasp concepts and related exercises. Basic educational activities are meant to establish a foundation of knowledge and/or competence that will be expanded upon in practice or in higher level activities. This webcast is available to global regulatory professionals for free.
Looking for More Euro-Centric Regulatory Content and Professional Development?Take a deeper dive into some of the most pressing issues impacting our community today—including Design Controls and Human Factors, Post Market Surveillance, and Data Management and Digitalization. Explore our up-coming European workshops produced in collaboration with the RAPS European Council (REC). Learn more and register. Join our RAPS CommunityRAPS membership provides vital information for regulatory professionals, as well as a place for networking and invaluable connections. Now is a great time to explore the many benefits to RAPS membership, including the Member Knowledge Center and our award-winning, private online community, Regulatory Exchange. Learn more about RAPS membership.How Do Webcasts Work?For the best webcast experience, please use the Google Chrome browser. RAPS webcasts are also mobile- and tablet-accessible for your convenience. Registrants will receive instructions on how to log in 24 hours before the start of the webcast. A live Q&A portion with the speaker will follow the presentation. Featured Speaker:Olga van Grol-Lawlor, principal regulatory affairs specialist, Boston Scientific
RAPS reserves the right to cancel this program at its sole discretion. RAPS will not be responsible for travel or other costs incurred due to cancellation.
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Cancellation Policy: Registration fees for this event are nonrefundable. Substitutions may be accepted with written approval from RAPS. If you have questions or concerns, please contact RAPS customer service at +1 301 770 2920, ext. 200, or via email at support@raps.org.