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 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.
Share your knowledge and expertise with your regulatory peers by submitting an in-depth, evidence-based article focusing on key areas and emerging issues in the global regulatory landscape.
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.
Registration is now open for RAPS Convergence 2021! Gather with the regulatory community 12-15 September for four days of learning, engagement, and excitement.
Keep the sparks coming! Delegates of the conference have access to on-demand content until the end of October 2021.
This updated edition is a great reference for anyone working in multinational product development and marketing.
Regipedia is an interactive resource created to benefit RAPS members with 24/7 access to more than 2,300 regulatory terms.
Hear from leaders around the globe as they share insights about their experiences and lessons learned throughout their certification journey.
Posted 09 December 2014 | By Alexander Gaffney, RAC,
The US Department of Health and Human Services (DHHS) is providing a gift to manufacturers of prospective vaccines meant to protect patients against the Ebola virus: Protection from legal liability.
In an announcement in the 9 December 2014 edition of the Federal Register, DHHS said it was issuing a new declaration that would "provide liability protection for activities related to Ebola virus disease vaccines consistent with the terms of the declaration."
Protection from legal liability is a major concern for vaccine manufacturers, whose products are administered to a large number of patients of different ages and health statuses. Even remarkably safe products can cause problems in a very small subset of patients, which becomes almost certain to happen when a vaccine is administered to tens of thousands—or even millions—of patients.
For ordinary vaccines, the US government offers legal protection through its National Vaccine Injury Compensation Program (NVICP) and a unique vaccine claims court system, both of which are funded through a tax assessed on vaccines.
For more background on this process, please see our explanation of a piece of vaccine liability legislation passed into law in June 2013.
But in emergency situations, the US government operates on a slightly different system. Under the Public Readiness and Emergency Preparedness (PREP) Act of 2005, DHHS is allowed to declare that a certain product is immune from liability as long as it is administered or used as a medical countermeasure in a specific patient population.
DHHS said it would use this same authority to allow all use of Ebola vaccines—barring, of course, "willful misconduct"—without concern to legal liability.
The liability waiver extends "without geographic limitation," DHHS noted, and is in effect for the next 12 months.
To date, no such vaccine products have been approved or made available for use through the US Food and Drug Administration's (FDA) Emergency Use Authorization (EUA) process, so for now DHHS' declaration seems anticipatory and intended to promote further research and development in this area.
Federal Register notice
Tags: Ebola, DHHS, Vaccine, Legal Liability
Regulatory Focus newsletters
All the biggest regulatory news and happenings.