Welcome to our new website! If this is the first time you are logging in on the new site, you will need to reset your password. Please contact us at raps@raps.org if you need assistance.
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.
Join the brightest minds in regulatory at the annual Regulatory Convergence. See the global regulatory community in action. Intensive workshops. Topical sessions. Meet ups with regulators. This is where it all comes together.
Learn how recent changes to the regulation of healthcare products in the EU will impact you as a regulatory professional.
In light of the COVID-19 pandemic, the RAC Board has elected to offer online testing with live online proctoring this summer.
The site navigation utilizes arrow, enter, escape, and space bar key commands. Left and right arrows move across top level links and expand / close menus in sub levels. Up and Down arrows will open main level menus and toggle through sub tier links. Enter and space open menus and escape closes them as well. Tab will move on to the next part of the site rather than go through menu items.
RAPS is closely monitoring developments in the Coronavirus (COVID-19) outbreak. See our public safety page for the latest updates.
Posted 02 May 2013 | By Louise Zornoza,
Brazil's National Health Surveillance Agency (Anvisa) has opened a Public Consultation on proposed Good Regulatory Practices (GRPs), which establishes the standards and procedures that are to be followed by the agency in the development of regulatory measures.
The proposals include a mechanism that would enable Anvisa to assess the best regulatory measure to achieve an intended regulatory goal, which would complement the Regulatory Impact Analysis process. That process is used to assesses the likely benefits, costs and impact of proposed regulations.
Anvisa said it sees the new consultation as part of a continuing process by which the agency will provide greater transparency on its regulatory conduct and responsibilities.
Anvisa: Anvisa lança Consulta Pública sobre Boas Práticas Regulatórias
Read all Breaking News from RegLink
Tags: brazil
Regulatory Focus newsletters
All the biggest regulatory news and happenings.