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Santa Clara, CA7/22/2017
Santa Clara, CA8/4/2017
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 European Medicines Agency (EMA) on Friday recommended the approval of eight new medicines after its Committee for Medicinal Products for Human Use (CHMP) met to discuss the drugs earlier this week.
The European Medicines Agency (EMA) on Friday said it plans to suspend the marketing authorization for three gadolinium contrast agents and restrict the use of others after a review by the agency's Pharmacovigilance Risk Assessment Committee (PRAC) confirmed evidence of gadolinium accumulation in patients' brains months after being injected.
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.
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By completing this form, I attest that I am eligible to take the RAC under the following criteria:
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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.
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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.