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.
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.
For 20 years, our flagship publication, Fundamentals of US Regulatory Affairs, has been giving regulatory professionals the insights and answers they need, right at their fingertips.
There are hundreds of RAC testing centers available worldwide. Any of the four RAC exams (US, EU, CAN or Global) may be taken at any location. Find an upcoming exam at a location near you.
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.
Posted 14 September 2012 | By Louise Zornoza,
Local Brazilian companies will be the beneficiaries of a new technology transfer regulation that is intended to reduce the country's dependence on foreign drug imports and technology.
The regulation, approved by the Board of Brazil's national regulatory agency, Anvisa, on 13 September 2012, establishes procedures for local companies to enter into drug development and technology transfer partnerships with the National Health Service (SUS). The regulation expands strategic and practical mechanisms for increasing access to new technologies in Brazil, and will lead to an estimated 25% reduction in the country's dependence on health sector imports.
According to Anvisa, proposed partnerships must have a, "High relevance for public health and for the development of the [Brazilian] health-industrial complex," and must be approved by Brazil's Ministry of Health. The new regulation has won the support of the Brazilian drug industry association, Farmabrasil.
Read more:
Read all Breaking News from RegLink
Tags: Imports, Transfer Regulation, Exports, Patents, pharmaceutical, brazil, drug
Regulatory Focus newsletters
All the biggest regulatory news and happenings.