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 firstname.lastname@example.org if you need assistance.
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.
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.
With so many global regulation changes, staying informed is a challenge. Join other regulatory professionals as you navigate the gray 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.
Posted 23 March 2012 | By Alexander Gaffney, RAC
The US Food and Drug Administration (FDA) announced Friday it will stop publishing written agreements and memoranda of understanding (MOU's) in the Federal Register, and will instead be opting to publish the agreement solely on its website.
The 23 March Federal Register final rule claims the existing regulatory policy is no longer necessary, and eliminates the requirement effective 6 August 2012.
FDA currently uses MOUs to generate agreements between US agencies and departments, as well as foreign governments and outside organizations.
The MOUs will henceforth be posted to one of three FDA webpages:
FDA has also published a companion Federal Register posting for all public comments on the rule "in the event we receive any significant adverse comments and withdraw this direct final rule."
Federal Register - Agreements and Memoranda of Understanding Between the Food and Drug Administration and Other Departments, Agencies, and Organizations (Final Rule)
Federal Register - Agreements and Memoranda of Understanding Between the Food and Drug Administration and Other Departments, Agencies, and Organizations (Companion Rule)
Tags: Memorandum of Understanding, Memoranda of Understanding, MOUs, MOU, Latest News, website
Regulatory Focus newsletters
All the biggest regulatory news and happenings.