RAC Certification and Study Group
The US RAC Study Group begins August 15th - Sign up now! We will be
meeting in Lakewood for 12 weeks every Wednesday. This is an
incredible opportunity to get a indepth knowledge of regulatory affairs.
We have historically had 90 to 100% pass rates on the test, however, you
do not have to take the test to attend the study group. All levels
of regulatory experience are welcome.
Each year RMRAS organizes a US RAC Study Groups to prepare our members for the US RAC Exam held in October/November.
The proposed dates and
times will be:
EU RAC - 10 Thursdays
starting August 14th and ending October 16th
US RAC - 10 Wednesdays
starting August 13th and ending October 15th.
Both classes 6:00 PM - 8:30
PM.
Costs to members:
Test details:
October and November held at numerous local computer based sites
Application deadlines:
August 15th = $325, and Late Registration September 8th = $375 (I always
hop on a computer with those interested after the first night of the
study group so they can save the $50.00)
If you are interested in the US RAC examination, please email
nancid@ecentral.com.
About the Regulatory Affairs Certification through the Regulatory Affairs Professionals Society (RAPS).
RAPS provides certification for the healthcare product RA community through its Regulatory Affairs Certification (RAC). The RAC designation is a mark of professional distinction. The RAC is indicative of the professional and technical abilities that are vital in this time of increasing challenges and demands within the health product sector.
Regulatory Affairs Certification (RAC) is a professional distinction that identifies individuals committed to excellence, the pursuit of knowledge and career advancement. The RAC is the only certification available to RA professionals within the healthcare product sector.
To become certified, individuals must pass the RAC examination, offered every year in April and November at worldwide locations. Three different certifications are available: RAC (CAN) for Canadian regulations, RAC (EU) for European regulations and RAC (US) for US regulations.
Currently, more than 3,000 RA professionals have earned the RAC designation, with many of them holding more than one regional credential (Canada, EU or US).
RAC-credentialed professionals are among the current and rising leaders in regulatory affairs in industry, government and academic organizations. It is intended for the regulatory affairs professional with three to five years of regulatory experience.
Why is Certification Desirable?
Certification sets those with the credential apart—or above—those without it. There are a number of advantages to seeking certification. Certification becomes a public recognition of professional achievement—both within and outside of the profession. For many, achieving certification becomes a personal professional goal—a way to test knowledge and to measure it against one’s peers. Others see certification as an aid to career advancement.
Exam Overview
- 100 multiple-choice questions for each of the RAC exams
- Two hours to complete each exam
- Administered by computer
- Administered only in English
The RAC Examinations are knowledge-based examinations addressing laws, regulations, policies and guidelines affecting regulated health products, including medical devices, pharmaceuticals, biologics and biotechnology in their respective regions. The examination is reviewed and revised annually.
For a comprehensive description of the RAC examinations, including procedures, format and a content outline visit www.raps.org for more information.