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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.
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.
Registration is now open for RAPS Euro Convergence 2021! Attend to join peers from EU and around the world to gain insights and exchange ideas on the regions most pressing issues.
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.
China has become the second-largest economy in the world and one of the most important markets for international businesses. As a regulatory professional, it is imperative to have a sufficient understanding of China’s NMPA regulations, processes, and expertise to navigate the NMPA system.
This workshop will focus on the fundamentals of Chinese NMPA regulations for medical device, providing a systematic review of all elements in the Chinese regulations from clinical trial, to quality management, product registration and post market surveillance. Led by instructors who are veteran regulatory managers, this workshop will also incorporate personal experience, knowledge, up to date information and best practices.
Pricing Amounts & Deadlines
18 November 2020 – 15 February 2021: Early Bird $800 Member | $900 Nonmember
16 February 2021 – 14 March 2021: Regular $900 Member | $1000 Nonmember
Who Should Attend?
This workshop is suitable for RA professionals with more than 3 years of experience, looking to broaden his/her knowledge base on international regulations or to focus on the Chinese market in the near future.
Faculty
Chang-Hong Whitney RAC MBA
President & CEO, Whitney Consulting Ltd.
Speakers to be added
Cancellation Policy
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.
All cancellation requests must be submitted in writing via our online cancellation form. RAPS is unable to accept cancellations by phone. Please specify the name of the person registered and event title.
Substitutions may be accepted with written approval from RAPS and must be submitted to raps@raps.org.
If you have questions or concerns, please contact RAPS customer service at +1 301 770 2920, ext. 200, or via email at raps@raps.org.