Login to access your membership accounts, education training and products and services.
Online1/4/2017 - 4/13/2017
RAPS Virtual Career Fairs are designed to connect employees with employers no matter where they might be located.
Local or global—RAPS has you covered with offices in Washington, DC, Shanghai and Singapore. There are RAPS chapters in Canada, Israel, Switzerland, Taiwan and throughout the United States, and local networks in Australia, Belgium, Brazil, Germany, India, Mexico, The Netherlands, Poland and Singapore.
Regulatory Exchange, aka RegEx, is where members come online to learn, grow and engage with a diverse global community of regulatory professionals with similar interests and goals.
It’s well-known that the National Institutes of Health (NIH) offers billions of dollars in grants to US academic research facilities. What’s less well-known is that each year, hundreds of new inventions are produced in the laboratories of NIH, the Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA), and these inventions are licensed out to private companies in the US and internationally for further research and development, with the hopes of bringing new products to market.
The ongoing overhaul of diagnostic and lab-developed test (LDT) regulations turned another corner last week, with Reps. Larry Bucshon, M.D. (R-IN) and Diana DeGette (D-CO) releasing a discussion draft of a bill that would offer a new direction for the US Food and Drug Administration (FDA) and the Centers for Medicare & Medicaid Services (CMS).
With the repeal of Obamacare on life support, the furor over rising prescription drug prices and President Donald Trump’s support for the cause could end up filling the vacant crossroads where bipartisanship meets change.
Welcome to Regulatory Reconnaissance, your daily regulatory news and intelligence briefing.
applying, all candidates must review the eligibility requirements and need to
complete an attestation to confirm that they meet at least one of the three
possible eligibility rules.
experience may include quality assurance, quality control, clinical research or health product project management.
First Name: Last Name:
By completing this form, I attest that I am eligible to take the RAC under the following criteria:
What exam are you applying for?
When would you like to take it?
By paying the RAC exam
registration fee, I agree to the following:
I have read, understood and
agree to comply with all policies outlined in the RAC Candidate Guide.
The information in my RAPS
account is complete and accurate.
I meet all eligibility
requirements for the RAC exam, and I authorize RAPS to make any inquiries
deemed necessary to verify my credentials. I understand that false information
may be cause for denial of this application or loss of the RAC credential.
I allow RAPS to use
information from my application and from the examination for the purpose of
aggregate statistical analysis, provided that any personal information or
identifiers are removed.
I understand and agree to the
policies related to withdrawing from the examination, presented in the
I acknowledge that I have
read and understand the tenets outlined in the RAPS Code of Ethics.